Figure 3.1
Drawing of the structure of cork from as it appeared under the microscope to Robert Hooke. The first scientific use of the word appears in this book.
Knowing the make up of cells and how cells work is necessary to all of the biological sciences. Learning about the similarities and differences between cell types is particularly important to the fields of cell biology and molecular biology. The importance of the similarities and differences between cell types is a unifying theme in biology. They allow the principles learned from studying one cell type to be applied when learning about other cell types. For example, learning about how single-celled animals or bacteria work can help us understand more about how human cells work. Research in cell biology is closely linked to genetics, biochemistry, molecular biology, and developmental biology.
A cell is the smallest unit that can carry out the processes of life. It is the basic unit of all living things, and all organisms are made up of one or more cells. In addition to having the same basic structure, all cells carry out similar life processes. These include transport of materials, obtaining and using energy, waste disposal, replication, and responding to their environment.
If you look at living organisms under a microscope you will see they are made up of cells. The word cell was first used by Robert Hooke, a British biologist and early microscopist. Hooke looked at thin slices of cork under a microscope. The structure he saw looked like a honeycomb as it was made up of many tiny units. Hooke’s drawing is shown in Figure below. In 1665 Hooke published his book Micrographia, in which he wrote:
Figure 3.1
Drawing of the structure of cork from as it appeared under the microscope to Robert Hooke. The first scientific use of the word appears in this book.
During the 1670s, the Dutch tradesman Antony van Leeuwenhoek, shown in Figure below, used microscopes to observe many microbes and body cells. Leeuwenhoek developed an interest in microscopy and ground his own lenses to make simple microscopes. Compound microscopes, which are microscopes that use more than one lens, had been invented around 1595. Several people, including Robert Hooke, had built compound microscopes and were making important discoveries with them during Leeuwenhoek’s time. These compound microscopes were very similar to the microscopes in use today. However, Leeuwenhoek was so good at making lenses that his simple microscopes were able to magnify much more clearly than the compound microscopes of his day. His microscope's increased ability to magnify over 200 times is comparable to a modern compound light microscope.
Leeuwenhoek was also very curious, and he took great care in writing detailed reports of what he saw under his microscope. He was the first person to report observations of many microscopic organisms. Some of his discoveries included tiny animals such as ciliates, foraminifera, roundworms, and rotifers, shown in Figure below. He discovered blood cells and was the first person to see living sperm cells. In 1683, Leeuwenhoek wrote to the Royal Society of London about his observations on the plaque between his own teeth, "a little white matter, which is as thick as if 'twere batter." He called the creatures he saw in the plaque animacules, or tiny animals. This report was among the first observations on living bacteria ever recorded.
Figure 3.2
Antony van Leeuwenhoek (1632-1723). His carefully crafted microscopes and insightful observations of microbes led to the title the "Father of Microscopy."
Figure 3.3
Rotifers, similar to the type that Leeuwenhoek saw under his microscope.
Hooke’s and Leeuwenhoek’s studies and observations filled people with wonder because their studies were of life forms that were everywhere, but too small to see with the naked eye. Just think how amazed you would be if you were to read about the first accounts of a newly discovered microorganism from the moon or Mars. Your first thought might be "Things can live there?!" which was probably the first thought of the people who read Hooke’s and Leeuwenhoek’s accounts. The microscope literally opened up an amazing new dimension in the natural sciences, and became a critical tool in the progress of biology.
Magnifying glasses had been in use since the 1300s, but the use of lenses to see very tiny objects was a slowly-developing technology. The magnification power of early microscopes was very limited by the glass quality used in the lenses and the amount of light reflected off the object. These early light microscopes had poor resolution and a magnification power of about 10 times. Compare this to the over 200 times magnification that Leeuwenhoek was able to achieve by carefully grinding his own lenses. However, in time the quality of microscopes was much improved with better lighting and resolution. It was through the use of light microscopes that the first discoveries about the cell and the cell theory (1839) were developed.
However, by the end of the 19th century, light microscopes had begun to hit resolution limits. Resolution is a measure of the clarity of an image; it is the minimum distance that two points can be separated by and still be distinguished as two separate points. Because light beams have a physical size, it is difficult to see an object that is about the same size as the wavelength of light. Objects smaller than about 0.2 micrometers appear fuzzy, and objects below that size just cannot be seen. Light microscopes were still useful, but most of the organelles and tiny cell structures discussed in later lessons were invisible to the light microscope.
Figure 3.4
Left to right: (a) Hookes light microscope (b) Modern electron microscope.
In the 1950s, a new system was developed that could use a beam of electrons to resolve very tiny dimensions at the molecular level. Electron microscopes, one of which is shown in Figure above, have been used to produce images of molecules and atoms. They have been used to visualize the tiny sub-cellular structures that were invisible to light microscopes. Many of the discoveries made about the cell since the 1950s have been made with electron microscopes.
Later, biologists found cells everywhere. Biologists in the early part of the 19th century suggested that all living things were made of cells, but the role of cells as the primary building block of life was not discovered until 1839 when two German scientists, Theodor Schwann, a zoologist, and Matthias Jakob Schleiden, a botanist, suggested that cells were the basic unit of all living things. Later, in 1858, the German doctor Rudolf Virchow observed that cells divide to produce more cells. He proposed that all cells arise only from other cells. The collective observations of all three scientists form the cell theory. The modern cell theory states that:
As with any theory, the cell theory is based on observations that over many years upheld the basic conclusions of Schwann’s paper written in 1839. However, one of Schwann’s original conclusions stated that cells formed in a similar way to crystals. This observation, which refers to spontaneous generation of life, was discounted when Virchow proposed that all cells arise only from other cells. The cell theory has withstood intense examination of cells by modern powerful microscopes and other instruments. Scientists use new techniques and equipment to look into cells to discover additional explanations for how they work.
Different cells within a single organism can come in a variety of sizes and shapes. They may not be very big, but their shapes can be very different from each other. However, these cells all have common abilities, such as getting and using food energy, responding to the external environment, and reproducing. A cell’s shape determines its function.
If cells have such an important job, why are they so small? And why are there no organisms with huge cells? The answers to these questions lie in a cell’s need for fast, easy food. The need to be able to pass nutrients and gases into and out of the cell sets a limit on how big cells can be. The larger a cell gets, the more difficult it is for nutrients and gases to move in and out of the cell.
As a cell grows, its volume increases more quickly than its surface area. If a cell was to get very large, the small surface area would not allow enough nutrients to enter the cell quickly enough for the cell’s needs. This idea is explained in Figure below. However, large cells have a way of dealing with some size challenges. Big cells, such as some white blood cells, often grow more nuclei so that they can supply enough proteins and RNA for the cell’s needs. Large, metabolically active cells often have lots of folds in their cell surface membrane. These folds increase the surface area available for transport into or out of the cell. Such cell types are found lining your small intestine, where they absorb nutrients from your food through little folds called microvilli.
Scale of Measurements
1 centimeter (cm) = 10 millimeters (mm) = 10-2 meters (m)
1 mm = 1000 micrometers (µm) = 10-3 m
1 µm = 1000 nanometers (nm) = 10-6 m
1 nm = 10-3 µm
Figure 3.5
A small cell (left), has a larger surface-area to volume ratio than a bigger cell (center). The greater the surface-area to volume ratio of a cell, the easier it is for the cell to get rid of wastes and take in essential materials such as oxygen and nutrients.
Imagine cells as little cube blocks. A small cube cell is one unit in length.
The total surface area of this cell is calculated by the equation:
height × width × number of sides × number of boxes
1 × 1 × 6 × 1 = 6
The volume of the cell is calculated:
height x width x length x number of boxes
1 × 1 × 1 × 1 = 1
The surface-area to volume ratio is:
area ÷ volume
6 ÷ 1=6
A larger cell that is 3 units in length would have a total surface area of
3 × 3 × 6 × 1 = 54
and a volume of:
3 × 3 × 3 × 1 = 27
The surface-area to volume ratio of the large cell is:
54÷ 27=2
Now, replace the three unit cell with enough one unit cells to equal the volume of the single three unit cell. This can be done with 27 one unit cells. Find the total surface area of the 27 cells:
1 × 1 × 6 × 27 = 162 units
The total volume of the block of 27 cells is:
1 × 1 × 1 × 27 = 27
The surface-area to volume ratio of the 27 cells is:
162 ÷ 27=6
An increased surface area to volume ratio means increased exposure to the environment. This means that nutrients and gases can move in and out of a small cell more easily than in and out of a larger cell.
The smallest prokaryotic cell currently known has a diameter of only 400 nm. Eukaryotic cells normally range between 1– 100 µm in diameter.
Figure 3.6
Ostrich eggs (a) can weigh as much as 1.5 kg, and be 13 cm in diameter, whereas each of the mouse cells (b) shown at right are each about 10 m in diameter, much smaller than the period at the end of this sentence.
The cells you have learned about so far are tinier than the period at the end of this sentence, so they are normally measured on a very tiny scale. Most cells are between 1 and 100 µm in diameter. The mouse cells in Figure above are about 10 µm in diameter. One exception however, is eggs. Eggs contain the largest known single cell, and the ostrich egg is the largest of them all. The ostrich egg in Figure above is over 10,000 times larger than the mouse cell.
Figure 3.7
Cells come in very different shapes. Left to right, top row: Long, thin nerve cells; biconcave red blood cells; curved-rod shaped bacteria. Left to right, bottom row: oval, flagellated algae and round, spiky pollen grains are just a sample of the many shapes.
The variety of cell shapes seen in prokaryotes and eukaryotes reflects the functions that each cell has. Each cell type has evolved a shape that best helps it survive and do its job. For example, the nerve cell in Figure above has long, thin extensions that reach out to other nerve cells. The extensions help the nerve cell pass chemical and electrical messages quickly through the body. The spikes on the pollen grain help it stick to a pollinating insect or animal so that it can be transferred to and pollinate another flower. The long whip-like flagella (tails) of the algae Chlamydomonas help it swim in water.
There are many different types of cells, but all cells have a few things in common. These are:
The cell membrane is the physical boundary between the inside of the cell (intracellular) and its outside environment (extracellular). It acts almost like the "skin" of the cell. Cytoplasm is the general term for all of the material inside the cell. Cytoplasm is made up of cytosol, a watery fluid that contains dissolved particles and organelles. Organelles are structures that carry out specific functions inside the cell. Ribosomes are the organelles on which proteins are made. Ribosomes are found throughout the cytosol of the cell. All cells also have DNA. DNA contains the genetic information needed for building structures such as proteins and RNA molecules in the cell.
There are two cell types: prokaryotes and eukaryotes. Prokaryotic cells are usually single-celled and smaller than eukaryotic cells. Eukaryotic cells are usually found in multicellular organisms, but there are some single-celled eukaryotes.
Figure 3.8
Diagram of a typical prokaryotic cell. Among other things, prokaryotic cells have a plasma membrane, cytoplasm, ribosomes, and DNA. Prokaryotes do not have membrane-bound organelles or a cell nucleus.
The bacterium in Figure above is a prokaryote. Prokaryotes are organisms that do not have a cell nucleus nor any organelles that are surrounded by a membrane. Some cell biologists consider the term "organelle" to describe membrane-bound structures only, whereas other cell biologists define organelles as discrete structures that have a specialized function. Prokaryotes have ribosomes, which are not surrounded by a membrane but do have a specialized function, and could therefore be considered organelles. Most of the metabolic functions carried out by a prokaryote take place in the plasma membrane.
Most prokaryotes are unicellular and have a cell wall that adds structural support and acts as a barrier against outside forces. Some prokaryotes have an extra layer outside their cell wall called a capsule, which helps them stick to surfaces or to each other. Prokaryotic DNA usually forms a circular molecule and is found in the cell’s cytoplasm along with ribosomes. Prokaryotic cells are very small; most are between 1–10 µm in diameter. They are found living in almost every environment on Earth. Biologists believe that prokaryotes were the first type of cells on Earth and that they are the most common organisms on Earth today.
Figure 3.9
A eukaryotic cell, represented here by a model animal cell is much more complex than a prokaryotic cell. Eukaryotic cells contain many organelles that do specific jobs. No single eukaryotic cell has all the organelles shown here, and this model shows all eukaryotic organelles.
A eukaryote is an organism whose cells are organized into complex structures by internal membranes and a cytoskeleton, as shown in Figure above. The most characteristic membrane-bound structure of eukaryotes is the nucleus. This feature gives them their name, which comes from Greek and means "true nucleus." The nucleus is the membrane-enclosed organelle that contains DNA. Eukaryotic DNA is organized in one or more linear molecules, called chromosomes. Some eukaryotes are single-celled, but many are multicellular.
In addition to having a plasma membrane, cytoplasm, a nucleus and ribosomes, eukaryotic cells also contain membrane-bound organelles. Each organelle in a eukaryote has a distinct function. Because of their complex level of organization, eukaryotic cells can carry out many more functions than prokaryotic cells. The main differences between prokaryotic and eukaryotic cells are shown in Figure below and listed in Table 1. Eukaryotic cells may or may not have a cell wall. Plant cells generally have cell walls, while animal cells do not.
Eukaryotic cells are about 10 times the size of a typical prokaryote; they range between 10 and 100 µm in diameter while prokaryotes range between 1 and 10 µm in diameter, as shown in Figure below. Scientists believe that eukaryotes developed about 1.6 – 2.1 billion years ago. The earliest fossils of multicellular organisms that have been found are 1.2 billion years old.
Figure 3.10
The relative scale of prokaryotic and eukaryotic cells. See how eukaryotic cells are generally 10 to 100 times larger than prokaryotic cells.
Figure 3.11
The main differences between prokaryotic and eukaryotic cells. Eukaryotic cells have membrane bound organelles while prokaryotic cells do not.
| Presence of | Prokaryote | Eukaryote |
| Plasma membrane | yes | yes |
| Genetic material (DNA) | yes | yes |
| Cytoplasm | yes | yes |
| Ribosomes | yes | yes |
| Nucleus | no | yes |
| Nucleolus | no | yes |
| Mitochondria | no | yes |
| Other membrane-bound organelles | no | yes |
| Cell wall | yes | some (not around animal cells) |
| Capsule | yes | no |
| Average diameter | 0.4 to 10 µm | 1 to 100 µm |
Are viruses prokaryotic or eukaryotic? Neither. Viruses are not made up of cells, so they do not have a cell membrane or any cytoplasm, ribosomes, or other organelles. Viruses do not replicate by themselves, instead, they use their host cell to make more of themselves. So most virologists consider viruses non-living. But, they do evolve, which is a characteristic of living things.
A virus is a sub-microscopic particle that can infect living cells. Viruses are much smaller than prokaryotic organisms. In essence, a virus is simply a nucleic acid surrounded by a protein coat. Viruses will be discussed in more detail in the Prokaryotes and Viruses chapter.
Figure 3.12
Structural overview of a virus, the T2 phage. A 2-dimensional representation is on the left, and a 3-dimensional representation is on the right. The virus is essentially nucleic acid surrounded by a protein coat.
Figure 3.13
Next we focus on cell structures and their roles.
The invention of the microscope opened up a previously unknown world. Before the invention of the microscope, very little was known about what made up living things and non-living things, or where living things came from. During Hooke’s and Leeuwenhoek’s time, spontaneous generation — the belief that living organisms grow directly from decaying organic substances — was the accepted explanation for the appearance of small organisms. For example, people accepted that mice spontaneously appeared in stored grain, and maggots formed in meat with no apparent external influence. Once cells were discovered, the search for answers to such questions as "what are cells made of?" and "what do they do?" became the focus of study.
Figure 3.14
The structure and contents of a typical animal cell. Every animal cell has a cell membrane, cytoplasm, and a nucleus, but not all cells have every structure shown here. For example, some cells such as red blood cells do not have any mitochondria, yet others such as muscle cells may have thousands of mitochondria.
Cells share the same needs: the need to get energy from their environment, the need to respond to their environment, and the need to reproduce. Cells must also be able to separate their relatively stable interior from the ever-changing external environment. They do this by coordinating many processes that are carried out in different parts of the cell. Structures that are common to many different cells indicate the common history shared by cell-based life. Examples of these common structures include the components of both the cell (or plasma) membrane and the cytoskeleton, and other structures shown in Figure above.
The plasma membrane (also called the cell membrane) has many functions. For example, it separates the internal environment of the cell from the outside environment. It allows only certain molecules into and out of the cell. The ability to allow only certain molecules in or out of the cell is referred to as selective permeability or semipermeability. These semipermeable membranes regulate the cell’s interactions between the internal cytoplasm and the external surroundings. Proteins that are associated with the plasma membrane determine which molecules can pass through the membrane. This will be discussed in the next lesson. The plasma membrane also acts as the attachment point for both the intracellular cytoskeleton and, if present, the cell wall.
The plasma membrane is a lipid bilayer that is common to all living cells. A lipid bilayer is a double layer of closely-packed lipid molecules. The membranes of cell organelles are also lipid bilayers. The plasma membrane contains many different biological molecules, mostly lipids and proteins. These lipids and proteins are involved in many cellular processes.
The main type of lipid found in the plasma membrane is phospholipid. A phospholipid is made up of a polar, phosphorus-containing head, and two long fatty acid, non-polar "tails." That is, the head of the molecule is hydrophilic (water-loving), and the tail is hydrophobic (water-fearing). Cytosol and extracellular fluid are made up of mostly water. In this watery environment, the water loving heads point out towards the water, and the water fearing tails point inwards, and push the water out. The resulting double layer is called a phospholipid bilayer. A phospholipid bilayer is made up of two layers of phospholipids, in which hydrophobic fatty acids are in the middle of the plasma membrane, and the hydrophilic heads are on the outside. An example of a simple phospholipid bilayer is illustrated in Figure below.
Figure 3.15
The hydrophobic fatty acids point towards the middle of the plasma membrane (pink), and the hydrophilic heads (blue) point outwards. The membrane is stabilized by cholesterol molecules (green). This self-organization of phospholipids results in a semipermeable membrane which allows only certain molecules in or out of the cell.
Plasma membranes of eukaryotes contain many proteins, as well as other lipids called sterols. The proteins have various functions, such as channels that allow certain molecules into the cell and receptors that bind to signal molecules. In Figure above, the smaller (green) molecules shown between the phospholipids are cholesterol molecules. Cholesterol helps keep the plasma membrane firm and stable over a wide range of temperatures. At least ten different types of lipids are commonly found in plasma membranes. Each type of cell or organelle will have a different percentage of each lipid, protein and carbohydrate.
Plasma membranes also contain certain types of proteins. A membrane protein is a protein molecule that is attached to, or associated with the membrane of a cell or an organelle. Membrane proteins can be put into two groups based on how the protein is associated with the membrane.
Integral membrane proteins are permanently embedded within the plasma membrane. They have a range of important functions. Such functions include channeling or transporting molecules across the membrane. Other integral proteins act as cell receptors. Integral membrane proteins can be classified according to their relationship with the bilayer:
Some integral membrane proteins are responsible for cell adhesion (sticking of a cell to another cell or surface). On the outside of cell membranes and attached to some of the proteins are carbohydrate chains that act as labels that identify the cell type. Shown in Figure below are two different types of membrane proteins and associated molecules.
Peripheral membrane proteins are proteins that are only temporarily associated with the membrane. They can be easily removed, which allows them to be involved in cell signaling. Peripheral proteins can also be attached to integral membrane proteins, or they can stick into a small portion of the lipid bilayer by themselves. Peripheral membrane proteins are often associated with ion channels and transmembrane receptors. Most peripheral membrane proteins are hydrophilic.
Figure 3.16
Some of the membrane proteins make up a major transport system that moves molecules and ions through the polar phospholipid bilayer.
In 1972 S.J. Singer and G.L. Nicolson proposed the now widely accepted Fluid Mosaic Model of the structure of cell membranes. The model proposes that integral membrane proteins are embedded in the phospholipid bilayer, as seen in Figure above. Some of these proteins extend all the way through the bilayer, and some only partially across it. These membrane proteins act as transport proteins and receptors proteins.
Their model also proposed that the membrane behaves like a fluid, rather than a solid. The proteins and lipids of the membrane move around the membrane, much like buoys in water. Such movement causes a constant change in the "mosaic pattern" of the plasma membrane.
The gel-like material within the cell that holds the organelles is called cytoplasm. The cytoplasm plays an important role in a cell, serving as a "jelly" in which organelles are suspended and held together by a fatty membrane. The cytosol, which is the watery substance that does not contain organelles, is made up of 80% to 90% water.
The cytosol plays a mechanical role by exerting pressure against the cell’s plasma membrane which helps keep the shape of the cell. Cytosol also acts as the site of biochemical reactions such as anaerobic glycolysis and protein synthesis. In prokaryotes all chemical reactions take place in the cytosol.
The cytoskeleton is a cellular "scaffolding" or "skeleton" that crisscrosses the cytoplasm. All eukaryotic cells have a cytoskeleton, and recent research has shown that prokaryotic cells also have a cytoskeleton. The eukaryotic cytoskeleton is made up of a network of long, thin protein fibers and has many functions. It helps to maintain cell shape. It holds organelles in place, and for some cells, it enables cell movement. The cytoskeleton also plays important roles in both the intracellular movement of substances and in cell division. Certain proteins act like a path that vesicles and organelles move along within the cell. The threadlike proteins that make up the cytoskeleton continually rebuild to adapt to the cell's constantly changing needs. Three main kinds of cytoskeleton fibers are microtubules, intermediate filaments, and microfilaments.
(a)The eukaryotic cytoskeleton. Microfilaments are shown in red, microtubules in green, and the nuclei are in blue. By linking regions of the cell together, the cytoskeleton helps support the shape of the cell. (b) Microscopy of keratin filaments (intermediate filaments) inside cells. (c) Microtubules in a methanol-fixated cell, visualized with anti-beta-tubuline antibodies.
| Microtubules | Intermediate Filaments | Microfilaments | |
| Fiber Diameter | About 25 nm | 8 to 11 nm | Around 7 nm |
| Protein Composition | Tubulin, with two subunits, alpha and beta tubulin | One of different types of proteins such as lamin, vimentin, and keratin | Actin |
| Shape | Hollow cylinders made of two protein chains twisted around each other | Protein fiber coils twisted into each other | Two actin chains twisted around one another |
| Main Functions | Organelle and vesicle movement; form mitotic spindles during cell reproduction; cell motility (in cilia and flagella) | Organize cell shape; positions organelles in cytoplasm structural support of the nuclear envelope and sarcomeres; involved in cell-to-cell and cell-to-matrix junctions | Keep cellular shape; allows movement of certain cells by forming cytoplasmatic extensions or contraction of actin fibers; involved in some cell-to-cell or cell-to-matrix junctions |
| Image |
Molecular structure of microtubules. |
Keratin intermediate filaments in skin cells (stained red). |
Actin cytoskeleton of mouse embryo cells. |
Flagella (flagellum, singular) are long, thin structures that stick out from the cell membrane. Both eukaryotic and prokaryotic cells can have flagella. Flagella help single-celled organisms move or swim towards food. The flagella of eukaryotic cells are normally used for movement too, such as in the movement of sperm cells. The flagella of either group are very different from each other. Prokaryotic flagella, shown below, are spiral-shaped and stiff. They spin around in a fixed base much like a screw does, which moves the cell in a tumbling fashion. Eukaryotic flagella are made of microtubules and bend and flex like a whip.
Bacterial flagella spin about in place, which causes the bacterial cell to "tumble."
Cilia (cilium, singular) are made up of extensions of the cell membrane that contain microtubules. Although both are used for movement, cilia are much shorter than flagella. Cilia cover the surface of some single-celled organisms, such as paramecium. Their cilia beat together to move the little animals through the water. In multicellular animals, including humans, cilia are usually found in large numbers on a single surface of cells. Multicellular animals' cilia usually move materials inside the body. For example, the mucociliary escalator of the respiratory system is made up of mucus-secreting cells that line the trachea and bronchi. Ciliated cells, shown in Figure below, move mucus away from the lungs. Spores, bacteria, and debris are caught in the mucus which is moved to the esophagus by the ciliated cells, where it is swallowed.
Figure 3.17
Left: Scanning electron micrograph (SEM), of the cilia sticking up from human lung cells. Right: Electron micrograph of cross-section of two cilia (not human), showing the positions of the microtubules inside. Note how there are nine groups of two microtubules (called dimers) in each cilium. Each dimer is made up of an alpha and a beta tubulin protein that are connected together.
The nucleus is a membrane-enclosed organelle found in most eukaryotic cells. The nucleus is the largest organelle in the cell and contains most of the cell's genetic information (mitochondria also contain DNA, called mitochondrial DNA, but it makes up just a small percentage of the cell’s overall DNA content). The genetic information, which contains the information for the structure and function of the organism, is found encoded in DNA in the form of genes. A gene is a short segment of DNA that contains information to encode an RNA molecule or a protein strand. DNA in the nucleus is organized in long linear strands that are attached to different proteins. These proteins help the DNA to coil up for better storage in the nucleus. Think how a string gets tightly coiled up if you twist one end while holding the other end. These long strands of coiled-up DNA and proteins are called chromosomes. Each chromosome contains many genes. The function of the nucleus is to maintain the integrity of these genes and to control the activities of the cell by regulating gene expression. Gene expression is the process by which the information in a gene is "decoded" by various cell molecules to produce a functional gene product, such as a protein molecule or an RNA molecule.
The degree of DNA coiling determines whether the chromosome strands are short and thick or long and thin. Between cell divisions, the DNA in chromosomes is more loosely coiled and forms long thin strands called chromatin. Before the cell divides, the chromatin coil up more tightly and form chromosomes. Only chromosomes stain clearly enough to be seen under a microscope. The word chromosome comes from the Greek word chroma, (color) and soma, (body) due to its ability to be stained strongly by dyes.
The nuclear envelope is a double membrane of the nucleus that encloses the genetic material. It separates the contents of the nucleus from the cytoplasm. The nuclear envelope is made of two lipid bilayers, an inner membrane and an outer membrane. The outer membrane is continuous with the rough endoplasmic reticulum. Many tiny holes called nuclear pores are found in the nuclear envelope. These nuclear pores help to regulate the exchange of materials (such as RNA and proteins) between the nucleus and the cytoplasm.
The nucleus of many cells also contains an organelle called a nucleolus, shown in Figure below. The nucleolus is mainly involved in the assembly of ribosomes. Ribosomes are organelles made of protein and ribosomal RNA (rRNA), and they build cellular proteins in the cytoplasm. The function of the rRNA is to provide a way of decoding the genetic messages within another type of RNA called mRNA, into amino acids. After being made in the nucleolus, ribosomes are exported to the cytoplasm where they direct protein synthesis.
Figure 3.18
The eukaryotic cell nucleus. Visible in this diagram are the ribosome-studded double membranes of the nuclear envelope, the DNA (as chromatin), and the nucleolus. Within the cell nucleus is a viscous liquid called nucleoplasm, similar to the cytoplasm found outside the nucleus. The chromatin (which is normally invisible), is visible in this figure only to show that it is spread out throughout the nucleus.
Centrioles are rod-like structures made of short microtubules. Nine groups of three microtubules make up each centriole. Two perpendicularly placed centrioles make up the centrosome. Centrioles are very important in cellular division, where they arrange the mitotic spindles that pull the chromosome apart during mitosis.
A mitochondrion (mitochondria, plural), is a membrane-enclosed organelle that is found in most eukaryotic cells. Mitochondria are called the "power plants" of the cell because they use energy from organic compounds to make ATP. ATP is the cell's energy source that is used for such things such as movement and cell division. Some ATP is made in the cytosol of the cell, but most of it is made inside mitochondria. The number of mitochondria in a cell depends on the cell’s energy needs. For example, active human muscle cells may have thousands of mitochondria, while less active red blood cells do not have any.
Figure 3.19
Electron micrograph of a single mitochondrion within which you can see many cristae. Mitochondria range from 1 to 10 m in size. This model of a mitochondrian shows the organized arrangement of the inner and outer membranes, the protein matrix, and the folded inner mitochondrial membranes.
As Figure above (a) and (b) shows, a mitochondrion has two phospholipids membranes. The smooth outer membrane separates the mitochondrion from the cytosol. The inner membrane has many folds, called cristae. The fluid-filled inside of the mitochondrian, called matrix, is where most of the cell’s ATP is made.
Although most of a cell's DNA is contained in the cell nucleus, mitochondria have their own DNA. Mitochandria are able to reproduce asexually and scientists think that they are descended from prokaryotes. According to the endosymbiotic theory, mitochondria were once free-living prokaryotes that infected ancient eukaryotic cells. The invading prokaryotes were protected inside the eukaryotic host cell, and in turn the prokaryote supplied extra ATP to its host.
The endoplasmic reticulum (ER) (plural, reticuli) is a network of phospholipid membranes that form hollow tubes, flattened sheets, and round sacs. These flattened, hollow folds and sacs are called cisternae. The ER has two major functions:
There are two types of endoplasmic reticulum, rough endoplasmic reticulum (RER) and smooth endoplasmic reticulum (SER).
Figure 3.20
Image of nucleus, endoplasmic reticulum and Golgi apparatus, and how they work together. The process of secretion from endoplasmic reticuli (orange) to Golgi apparatus (pink) is shown.
Ribosomes are small organelles and are the site of protein synthesis (or assembly). They are made of ribosomal protein and ribosomal RNA. Each ribosome has two parts, a large and a small subunit, as shown in Figure below. The subunits are attached to each other. Ribosomes can be found alone or in groups within the cytoplasm. Some ribosomes are attached to the endoplasmic reticulum (as shown in Figure above), and others are attached to the nuclear envelope.
Ribozymes are RNA molecules that catalyzes chemical reactions, such as translation. Translation is the process of ordering the amino acids in the assembly of a protein, and more will be discussed on translation in a later chapter. Briefly, the ribosomes interact with other RNA molecules to make chains of amino acids called polypeptide chains, due to the peptide bond that forms between individual amino acids. Polypeptide chains are built from the genetic instructions held within a messenger RNA molecule. Polypeptide chains that are made on the rough ER are inserted directly into the ER and then are transported to their various cellular destinations. Ribosomes on the rough ER usually produce proteins that are destined for the cell membrane.
Figure 3.21
The two subunits that make up a ribosome, small organelles that are intercellular protein factories.
The Golgi apparatus is a large organelle that is usually made up of five to eight cup-shaped, membrane-covered discs called cisternae, as shown in Figure above. The cisternae look a bit like a stack of deflated balloons. The Golgi apparatus modifies, sorts, and packages different substances for secretion out of the cell, or for use within the cell. The Golgi apparatus is found close to the nucleus of the cell where it modifies proteins that have been delivered in transport vesicles from the RER. It is also involved in the transport of lipids around the cell. Pieces of the Golgi membrane pinch off to form vesicles that transport molecules around the cell. The Golgi apparatus can be thought of as similar to a post office; it packages and labels "items" and then sends them to different parts of the cell. Both plant and animal cells have a Golgi apparatus. Plant cells can have up to several hundred Golgi stacks scattered throughout the cytoplasm. In plants, the Golgi apparatus contains enzymes that synthesize some of the cell wall polysaccharides.
A vesicle is a small, spherical compartment that is separated from the cytosol by at least one lipid bilayer. Many vesicles are made in the Golgi apparatus and the endoplasmic reticulum, or are made from parts of the cell membrane. Vesicles from the Golgi apparatus can be seen in Figure above. Because it is separated from the cytosol, the space inside the vesicle can be made to be chemically different from the cytosol. Vesicles are basic tools of the cell for organizing metabolism, transport, and storage of molecules. Vesicles are also used as chemical reaction chambers. They can be classified by their contents and function.
Vacuoles are membrane-bound organelles that can have secretory, excretory, and storage functions. Many organisms will use vacuoles as storage areas and some plant cells have very large vacuoles. Vesicles are much smaller than vacuoles and function in transporting materials both within and to the outside of the cell.
Most of the organelles that have been discussed are common to both animal and plant cells. However, plant cells also have features that animal cells do not have; they have a cell wall, a large central vacuole, and plastids such as chloroplasts.
Plants have very different lifestyles from animals, and these differences are apparent when you examine the structure of the plant cell. Plants make their own food in a process called photosynthesis. They take in carbon dioxide (CO2) and water (H2O) and convert them into sugars. The features unique to plant cells can be seen in Figure below.
Figure 3.22
In addition to containing most of the organelles found in animal cells, plant cells also have a cell wall, a large central vacuole, and plastids. These three features are not found in animal cells.
A cell wall is a rigid layer that is found outside the cell membrane and surrounds the cell. The cell wall contains not only cellulose and protein, but other polysaccharides as well. In fact, two other classes of polysaccharides, hemicelluloses and pectic polysaccharides, can comprise 30% of the dry mass of the cell wall. The cell wall provides structural support and protection. Pores in the cell wall allow water and nutrients to move into and out of the cell. The cell wall also prevents the plant cell from bursting when water enters the cell.
Microtubules guide the formation of the plant cell wall. Cellulose is laid down by enzymes to form the primary cell wall. Some plants also have a secondary cell wall. The secondary wall contains a lignin, a secondary cell component in plant cells that have completed cell growth/expansion.
Most mature plant cells have a central vacuole that occupies more than 30% of the cell's volume, but can also occupy as much as 90% of the volume of certain cells. The central vacuole is surrounded by a membrane called the tonoplast. The central vacuole has many functions. Aside from storage, the main role of the vacuole is to maintain turgor pressure against the cell wall. Proteins found in the tonoplast control the flow of water into and out of the vacuole. The central vacuole also stores the pigments that color flowers.
The central vacuole contains large amounts of a liquid called cell sap, which differs in composition to the cell cytosol. Cell sap is a mixture of water, enzymes, ions, salts, and other substances. Cell sap may also contain toxic byproducts that have been removed from the cytosol. Toxins in the vacuole may help to protect some plants from being eaten.
Plant plastids are a group of closely related membrane-bound organelles that carry out many functions. They are responsible for photosynthesis, for storage of products such as starch, and for the synthesis of many types of molecules that are needed as cellular building blocks. Plastids have the ability to change their function between these and other forms. Plastids contain their own DNA and some ribosomes, and scientists think that plastids are descended from photosynthetic bacteria that allowed the first eukaryotes to make oxygen. The main types of plastids and their functions are:
Figure 3.23
Plant cells with visible chloroplasts (left). Starch-storing potato leucoplasts (right).
Figure 3.24
The internal structure of a chloroplast, with a granal stack of thylakoids circled.
Chloroplasts capture light energy from the sun and use it with water and carbon dioxide to produce sugars for food. Chloroplasts look like flat discs that are usually 2 to 10 micrometers in diameter and 1 micrometer thick. A model of a chloroplast is shown in Figure above. The chloroplast is enclosed by an inner and an outer phospholipid membrane. Between these two layers is the intermembrane space. The fluid within the chloroplast is called the stroma, and it contains one or more molecules of small circular DNA. The stroma also has ribosomes. Within the stroma are stacks of thylakoids, the sub-organelles which are the site of photosynthesis. The thylakoids are arranged in stacks called grana (singular: granum). A thylakoid has a flattened disk shape. Inside it is an empty area called the thylakoid space or lumen. Photosynthesis takes place on the thylakoid membrane.
Within the thylakoid membrane is the complex of proteins and light-absorbing pigments, such as chlorophyll and carotenoids. This complex allows capture of light energy from many wavelengths because chlorophyll and carotenoids both absorb different wavelengths of light. You will learn more about how chloroplasts convert light energy into chemical energy in the Photosynthesis chapter.
Biological organization exists at all levels in organisms. It can be seen at the smallest level, in the molecules that made up such things as DNA and proteins, to the largest level, in an organism such as a blue whale, the largest mammal on Earth. Similarly, single celled prokaryotes and eukaryotes show order in the way their cells are arranged. Single-celled organisms such as an amoeba are free-floating and independent-living. Their single-celled "bodies" are able to carry out all the processes of life such as metabolism and respiration without help from other cells. Some single-celled organisms such as bacteria can group together and form a biofilm. A biofilm is a large grouping of many bacteria that sticks to a surface and makes a protective coating over itself. Biofilms can show similarities to multicellular organisms. Division of labor is the process in which one group of cells does one job (such as making the "glue" that sticks the biofilm to the surface) while another group of cells does another job (such as taking in nutrients). Multicellular organisms carry out their life processes through division of labor and they have specialized cells that do specific jobs. However, biofilms are not considered a multicellular organism and are instead called colonial organisms. The difference between a multicellular organism and a colonial organism is that individual organisms from a colony or biofilm can, if separated, survive on their own, while cells from a multicellular organism (e.g., liver cells) cannot.
Figure 3.25
Colonial algae of the genus .
Colonial organisms were probably one of the first evolutionary steps towards multicellular organisms. Algae of the genus Volvox are an example of the border between colonial organisms and multicellular organisms.
Each Volvox, shown in Figure above, is a colonial organism. It is made up of between 1000 to 3000 photosynthetic algae that are grouped together into a hollow sphere. The sphere has a distinct front and back end. The cells have eyespots, which are more developed in the cells near the front. This enables the colony to swim towards light.
The oldest known multicellular organism is a red algae Bangiomorpha pubescens, fossils of which were found in 1.2 billion year old rock. However, the first organisms were single celled. How multicellular organisms developed is the subject of much debate.
Scientists think that multicellularity arose from cooperation between many organisms of the same species. The Colonial Theory proposes that this cooperation led to the development of a multicellular organism. Many examples of cooperation between organisms in nature have been observed. For example, a certain species of amoeba (a single-celled animal) groups together during times of food shortage and forms a colony that moves as one to a new location. Some of these amoebas then become slightly differentiated from each other. Volvox, shown in Figure above, is another example of a colonial organism. Most scientists accept that the Colonial theory explains how multicellular organisms evolved.
Multicellular organisms are organisms that are made up of more than one type of cell and have specialized cells that are grouped together to carry out specialized functions. Most life that you can see without a microscope is multicellular. As discussed earlier, the cells of a multicellular organism would not survive as independent cells. The body of a multicellular organism, such as a tree or a cat, exhibits organization at several levels: tissues, organs, and organ systems. Similar cells are grouped into tissues, groups of tissues make up organs, and organs with a similar function are grouped into an organ system.
The simplest living multicellular organisms, sponges, are made of many specialized types of cells that work together for a common goal. Such cell types include digestive cells, tubular pore cells; and epidermal cells. Though the different cell types create a large organized, multicellular structure—the visible sponge—they are not organized into true interconnected tissues. If a sponge is broken up by passing it through a sieve, the sponge will reform on the other side. However, if the sponge’s cells are separated from each other, the individual cell types cannot survive alone. Simpler colonial organisms, such as members of the genus Volvox, as shown in Figure above, differ in that their individual cells are free-living and can survive on their own if separated from the colony.
Figure 3.26
This roundworm, a multicellular organism, was stained to highlight the nuclei of all the cells in its body (red dots).
A tissue is a group of connected cells that have a similar function within an organism. More complex organisms such as jellyfish, coral, and sea anemones have a tissue level of organization. For example, jellyfish have tissues that have separate protective, digestive, and sensory functions.
Even more complex organisms, such as the roundworm shown in Figure above, while also having differentiated cells and tissues, have an organ level of development. An organ is a group of tissues that has a specific function or group of functions. Organs can be as primitive as the brain of a flatworm (a group of nerve cells), as large as the stem of a sequoia (up to 90 meters, or 300 feet, in height), or as complex as a human liver.
The most complex organisms (such as mammals, trees, and flowers) have organ systems. An organ system is a group of organs that act together to carry out complex related functions, with each organ focusing on a part of the task. An example is the human digestive system in which the mouth ingests food, the stomach crushes and liquifies it, the pancreas and gall bladder make and release digestive enzymes, and the intestines absorb nutrients into the blood.
Probably the most important feature of a cell’s phospholipid membranes is that they are selectively permeable. A membrane that is selectively permeable has control over what molecules or ions can enter or leave the cell, as shown in Figure below. The permeability of a membrane is dependent on the organization and characteristics of the membrane lipids and proteins. In this way, cell membranes help maintain a state of homeostasis within cells (and tissues, organs, and organ systems) so that an organism can stay alive and healthy.
Figure 3.27
A selectively permeable membrane allows certain molecules through, but not others.
The molecular make-up of the phospholipid bilayer limits the types of molecules that can pass through it. For example, hydrophobic (water-hating) molecules, such as carbon dioxide (CO2) and oxygen (O2), can easily pass through the lipid bilayer, but ions such as calcium (Ca2+) and polar molecules such as water (H2O) cannot. The hydrophobic interior of the phospholipid does not allow ions or polar molecules through because they are hydrophilic, or water loving. In addition, large molecules such as sugars and proteins are too big to pass through the bilayer. Transport proteins within the membrane allow these molecules to cross the membrane into or out of the cell. This way, polar molecules avoid contact with the nonpolar interior of the membrane, and large molecules are moved through large pores.
Every cell is contained within a membrane punctuated with transport proteins that act as channels or pumps to let in or force out certain molecules. The purpose of the transport proteins is to protect the cell's internal environment and to keep its balance of salts, nutrients, and proteins within a range that keeps the cell and the organism alive.
There are three main ways that molecules can pass through a phospholipid membrane. The first way requires no energy input by the cell and is called passive transport. The second way requires that the cell uses energy to pull in or pump out certain molecules and ions and is called active transport. The third way is through vesicle transport, in which large molecules are moved across the membrane in bubble-like sacks that are made from pieces of the membrane.
Passive transport is a way that small molecules or ions move across the cell membrane without input of energy by the cell. The three main kinds of passive transport are diffusion, osmosis, and facilitated diffusion.
Diffusion is the movement of molecules from an area of high concentration of the molecules to an area with a lower concentration. The difference in the concentrations of the molecules in the two areas is called the concentration gradient. Diffusion will continue until this gradient has been eliminated. Since diffusion moves materials from an area of higher concentration to the lower, it is described as moving solutes "down the concentration gradient." The end result of diffusion is an equal concentration, or equilibrium, of molecules on both sides of the membrane.
If a molecule can pass freely through a cell membrane, it will cross the membrane by diffusion (Figure below).
Figure 3.28
Molecules move from an area of high concentration to an area of lower concentration until an equilibrium is met. The molecules continue to cross the membrane at equilibrium, but at equal rates in both directions.
Imagine you have a cup that has 100ml water, and you add 15g of table sugar to the water. The sugar dissolves and the mixture that is now in the cup is made up of a solute (the sugar), that is dissolved in the solvent (the water). The mixture of a solute in a solvent is called a solution.
Imagine now that you have a second cup with 100ml of water, and you add 45 grams of table sugar to the water. Just like the first cup, the sugar is the solute, and the water is the solvent. But now you have two mixtures of different solute concentrations. In comparing two solutions of unequal solute concentration, the solution with the higher solute concentration is hypertonic, and the solution with the lower concentration is hypotonic. Solutions of equal solute concentration are isotonic. The first sugar solution is hypotonic to the second solution. The second sugar solution is hypertonic to the first.
You now add the two solutions to a beaker that has been divided by a selectively permeable membrane. The pores in the membrane are too small for the sugar molecules to pass through, but are big enough for the water molecules to pass through. The hypertonic solution is on one side of the membrane and the hypotonic solution on the other. The hypertonic solution has a lower water concentration than the hypotonic solution, so a concentration gradient of water now exists across the membrane. Water molecules will move from the side of higher water concentration to the side of lower concentration until both solutions are isotonic.
Osmosis is the diffusion of water molecules across a selectively permeable membrane from an area of higher concentration to an area of lower concentration. Water moves into and out of cells by osmosis. If a cell is in a hypertonic solution, the solution has a lower water concentration than the cell cytosol does, and water moves out of the cell until both solutions are isotonic. Cells placed in a hypotonic solution will take in water across their membrane until both the external solution and the cytosol are isotonic.
A cell that does not have a rigid cell wall (such as a red blood cell), will swell and lyse (burst) when placed in a hypotonic solution. Cells with a cell wall will swell when placed in a hypotonic solution, but once the cell is turgid (firm), the tough cell wall prevents any more water from entering the cell. When placed in a hypertonic solution, a cell without a cell wall will lose water to the environment, shrivel, and probably die. In a hypertonic solution, a cell with a cell wall will lose water too. The plasma membrane pulls away from the cell wall as it shrivels. The cell becomes plasmolyzed. Animal cells tend to do best in an isotonic environment, plant cells tend to do best in a hypotonic environment. This is demonstrated in Figure below.
Figure 3.29
Unless an animal cell (such as the red blood cell in the top panel) has an adaptation that allows it to alter the osmotic uptake of water, it will lose too much water and shrivel up in a hypertonic environment. If placed in a hypotonic solution, water molecules will enter the cell causing it to swell and burst. Plant cells (bottom panel) become plasmolyzed in a hypertonic solution, but tend to do best in a hypotonic environment. Water is stored in the central vacuole of the plant cell.
When water moves into a cell by osmosis, osmotic pressure may build up inside the cell. If a cell has a cell wall, the wall helps maintain the cell’s water balance. Osmotic pressure is the main cause of support in many plants. When a plant cell is in a hypotonic environment, the osmotic entry of water raises the turgor pressure exerted against the cell wall until the pressure prevents more water from coming into the cell. At this point the plant cell is turgid. The effects of osmotic pressures on plant cells are shown in Figure below.
Figure 3.30
The central vacuoles of the plant cells in the left image are full of water, so the cells are turgid. The plant cells in the right image have been exposed to a hypertonic solution; water has left the central vacuole and the cells have become plasmolysed.
Osmosis can be seen very effectively when potato slices are added to a high concentration of salt solution (hypertonic). The water from inside the potato moves out of the potato cells to the salt solution, which causes the potato cells to lose turgor pressure. The more concentrated the salt solution, the greater the difference in the size and weight of the potato slice after plasmolysis.
The action of osmosis can be very harmful to organisms, especially ones without cell walls. For example, if a saltwater fish (whose cells are isotonic with seawater), is placed in fresh water, its cells will take on excess water, lyse, and the fish will die. Another example of a harmful osmotic effect is the use of table salt to kill slugs and snails.
Organisms that live in a hypotonic environment such as freshwater, need a way to prevent their cells from taking in too much water by osmosis. A contractile vacuole is a type of vacuole that removes excess water from a cell. Freshwater protists, such as the paramecia shown in Figure below, have a contractile vacuole. The vacuole is surrounded by several canals, which absorb water by osmosis from the cytoplasm. After the canals fill with water, the water is pumped into the vacuole. When the vacuole is full, it pushes the water out of the cell through a pore. Other protists, such as members of the genus Amoeba, have contractile vacuoles that move to the surface of the cell when full and release the water into the environment.
Figure 3.31
The contractile vacuole is the star-like structure within the paramecia (at center-right)
Facilitated diffusion is the diffusion of solutes through transport proteins in the plasma membrane. Facilitated diffusion is a type of passive transport. Even though facilitated diffusion involves transport proteins, it is still passive transport because the solute is moving down the concentration gradient.
As was mentioned earlier, small nonpolar molecules can easily diffuse across the cell membrane. However, due to the hydrophobic nature of the lipids that make up cell membranes, polar molecules (such as water) and ions cannot do so. Instead, they diffuse across the membrane through transport proteins. A transport protein completely spans the membrane, and allows certain molecules or ions to diffuse across the membrane. Channel proteins, gated channel proteins, and carrier proteins are three types of transport proteins that are involved in facilitated diffusion.
A channel protein, a type of transport protein, acts like a pore in the membrane that lets water molecules or small ions through quickly. Water channel proteins allow water to diffuse across the membrane at a very fast rate. Ion channel proteins allow ions to diffuse across the membrane.
A gated channel protein is a transport protein that opens a "gate," allowing a molecule to pass through the membrane. Gated channels have a binding site that is specific for a given molecule or ion. A stimulus causes the "gate" to open or shut. The stimulus may be chemical or electrical signals, temperature, or mechanical force, depending on the type of gated channel. For example, the sodium gated channels of a nerve cell are stimulated by a chemical signal which causes them to open and allow sodium ions into the cell. Glucose molecules are too big to diffuse through the plasma membrane easily, so they are moved across the membrane through gated channels. In this way glucose diffuses very quickly across a cell membrane, which is important because many cells depend on glucose for energy.
A carrier protein is a transport protein that is specific for an ion, molecule, or group of substances. Carrier proteins "carry" the ion or molecule across the membrane by changing shape after the binding of the ion or molecule. Carrier proteins are involved in passive and active transport. A model of a channel protein and carrier proteins is shown in Figure below.
Figure 3.32
Facilitated diffusion in cell membrane. Channel proteins and carrier proteins are shown (but not a gated-channel protein). Water molecules and ions move through channel proteins. Other ions or molecules are also carried across the cell membrane by carrier proteins. The ion or molecule binds to the active site of a carrier protein. The carrier protein changes shape, and releases the ion or molecule on the other side of the membrane. The carrier protein then returns to its original shape.
Ions such as sodium (Na+), potassium (K-), calcium (Ca2+), and chloride (Cl-), are important for many cell functions. Because they are polar, these ions do not diffuse through the membrane. Instead they move through ion channel proteins where they are protected from the hydrophobic interior of the membrane. Ion channels allow the formation of a concentration gradient between the extracellular fluid and the cytosol. Ion channels are very specific as they allow only certain ions through the cell membrane. Some ion channels are always open, others are "gated" and can be opened or closed. Gated ion channels can open or close in response to different types of stimuli such as electrical or chemical signals.
In contrast to facilitated diffusion which does not require energy and carries molecules or ions down a concentration gradient, active transport pumps molecules and ions against a concentration gradient. Sometimes an organism needs to transport something against a concentration gradient. The only way this can be done is through active transport which uses energy that is produced by respiration (ATP). In active transport, the particles move across a cell membrane from a lower concentration to a higher concentration. Active transport is the energy-requiring process of pumping molecules and ions across membranes "uphill" against a gradient.
Carrier proteins can work with a concentration gradient (passive transport), but some carrier proteins can move solutes against the concentration gradient (from high concentration to low), with energy input from ATP. As in other types of cellular activities, ATP supplies the energy for most active transport. One way ATP powers active transport is by transferring a phosphate group directly to a carrier protein. This may cause the carrier protein to change its shape, which moves the molecule or ion to the other side of the membrane. An example of this type of active transport system, as shown in Figure below, is the sodium-potassium pump, which exchanges sodium ions for potassium ions across the plasma membrane of animal cells.
Figure 3.33
The sodium-potassium pump system moves sodium and potassium ions against large concentration gradients. It moves two potassium ions into the cell where potassium levels are high, and pumps three sodium ions out of the cell and into the extracellular fluid.
As is shown in Figure above, three sodium ions bind with the protein pump inside the cell. The carrier protein then gets energy from ATP and changes shape. In doing so, it pumps the three sodium ions out of the cell. At that point, two potassium ions move in from outside the cell and bind to the protein pump. The sodium-potassium pump is found in the plasma membrane of almost every human cell and is common to all cellular life. It helps maintain cell potential and regulates cellular volume. Cystic fibrosis is a genetic disorder that results in a misshapen chloride ion pump. Chloride levels within the cells are not controlled properly, and the cells produce thick mucus. The chloride ion pump is important for creating sweat, digestive juices, and mucus.
The active transport of ions across the membrane causes an electrical gradient to build up across the plasma membrane. The number of positively charged ions outside the cell is greater than the number of positively charged ions in the cytosol. This results in a relatively negative charge on the inside of the membrane, and a positive charge on the outside. This difference in charges causes a voltage across the membrane. Voltage is electrical potential energy that is caused by a separation of opposite charges, in this case across the membrane. The voltage across a membrane is called membrane potential. Membrane potential is very important for the conduction of electrical impulses along nerve cells.
Because the inside of the cell is negative compared to outside the cell, the membrane potential favors the movement of positively charged ions (cations) into the cell, and the movement of negative ions (anions) out of the cell. So, there are two forces that drive the diffusion of ions across the plasma membrane—a chemical force (the ions' concentration gradient), and an electrical force (the effect of the membrane potential on the ions’ movement). These two forces working together are called an electrochemical gradient, and will be discussed in detail in the chapter Nervous and Endocrine Systems.
Some molecules or particles are just too large to pass through the plasma membrane or to move through a transport protein. So cells use two other methods to move these macromolecules (large molecules) into or out of the cell. Vesicles or other bodies in the cytoplasm move macromolecules or large particles across the plasma membrane. There are two types of vesicle transport, endocytosis and exocytosis.
Endocytosis is the process of capturing a substance or particle from outside the cell by engulfing it with the cell membrane. The membrane folds over the substance and it becomes completely enclosed by the membrane. At this point a membrane-bound sac, or vesicle pinches off and moves the substance into the cytosol. There are two main kinds of endocytosis:
Figure 3.34
Transmission electron microscope image of brain tissue that shows pinocytotic vesicles. Pinocytosis is a type of endocytosis.
Figure 3.35
Mode of exocytosis at a synaptic junction, where two nerve cells meet. Chemical signal molecules are released from nerve cell A by exocytosis, and move toward receptors in nerve cell B. Exocytosis is an important part in cell signaling.
Exocytosis describes the process of vesicles fusing with the plasma membrane and releasing their contents to the outside of the cell, as shown in Figure above. Exocytosis occurs when a cell produces substances for export, such as a protein, or when the cell is getting rid of a waste product or a toxin. Newly made membrane proteins and membrane lipids are moved on top the plasma membrane by exocytosis. For a detailed animation on cellular secretion, see http://vcell.ndsu.edu/animations/constitutivesecretion/first.htm.
Homeostasis refers to the balance, or equilibrium within the cell or a body. It is an organism’s ability to keep a constant internal environment. Keeping a stable internal environment requires constant adjustments as conditions change inside and outside the cell. The adjusting of systems within a cell is called homeostatic regulation. Because the internal and external environments of a cell are constantly changing, adjustments must be made continuously to stay at or near the set point (the normal level or range). Homeostasis is a dynamic equilibrium rather than an unchanging state. The cellular processes discussed in this lesson all play an important role in homeostatic regulation. You will learn more about homeostasis in The Human Body chapter.
To survive and grow, cells need to be able to "talk" with their cell neighbors and be able to detect change in their environment. Talking with neighbors is even more important to a cell if it is part of a multicellular organism. The billions of cells that make up your body need to be able to communicate with each other to allow your body to grow, and to keep you alive and healthy. The same is true for any organism. Cell signaling is a major area of research in biology today. Recently scientists have discovered that many different cell types, from bacteria to plants, use similar types of communication pathways, or cell-signaling mechanisms. This suggests that cell-signaling mechanisms evolved long before the first multicellular organism did.
For cells to be able to signal to each other, a few things are needed:
Cells that are communicating may be right next to each other or far apart. The type of chemical signal a cell will send differs depending on the distance the message needs to go. For example, hormones, ions, and neurotransmitters are all types of signals that are sent depending on the distance the message needs to go.
The target cell then needs to be able to recognize the signal. Chemical signals are received by the target cell on receptor proteins. As discussed earlier, most receptor proteins are found in the plasma membrane. Most receptors proteins are found on the plasma membrane, but some are also found inside the cell. These receptor proteins are very specific for only one particular signal molecule, much like a lock that recognizes only one key. Therefore, a cell has lots of receptor proteins to recognize the large number of cell signal molecules. There are three stages to sending and receiving a cell "message:" reception, transduction, and response.
Cell-surface receptors are integral proteins—they reach right through the lipid bilayer, spanning from the outside to the inside of the cell. These receptor proteins are specific for just one kind of signal molecule. The signaling molecule acts as a ligand when it binds to a receptor protein. A ligand is a small molecule that binds to a larger molecule. Signal molecule binding causes the receptor protein to change its shape. At this point the receptor protein can interact with another molecule. The ligand (signal molecule) itself does not pass through the plasma membrane.
In eukaryotic cells, most of the intracellular proteins that are activated by a ligand binding to a receptor protein are enzymes. Receptor proteins are named after the type of enzyme that they interact with inside the cell. These enzymes include G proteins and protein kinases, likewise there are G-protein-linked receptors and tyrosine kinase receptors. A kinase is a protein involved in phosphorylation. A G-protein linked receptor is a receptor that works with the help of a protein called a G-protein. A G-protein gets its name from the molecule to which it is attached, guanosine triphosphate (GTP), or guanosine diphosphate (GDP). The GTP molecule is similar to ATP.
Once G proteins or protein kinase enzymes are activated by a receptor protein, they create molecules called second messengers. A second messenger is a small molecule that starts a change inside a cell in response to the binding of a specific signal to a receptor protein. Some second messenger molecules include small molecules called cyclic nucleotides, such as cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP). Calcium ions (Ca2+) also act as secondary messengers. Secondary messengers are a part of signal transduction pathways.
A signal-transduction pathway is the signaling mechanism by which a cell changes a signal on it surface into a specific response inside the cell. It most often involves an ordered sequence of chemical reactions inside the cell which is carried out by enzymes and other molecules. In many signal transduction processes, the number of proteins and other molecules participating in these events increases as the process progresses from the binding of the signal. A "signal cascade" begins. Think of a signal cascade as a chemical domino-effect inside the cell, in which one domino knocks over two dominos, which in turn knock over four dominos, and so on. The advantage of this type of signaling to the cell is that the message from one little signal molecule can be greatly amplified and have a dramatic effect.
Figure 3.36
How a G-protein linked receptor works with the help of a G-protein. In panel C, the second messenger cAMP can be seen moving away from the enzyme.
G protein-linked receptors are only found in higher eukaryotes, including yeast, plants, and animals. Your senses of sight and smell are dependent on G-protein linked receptors. The ligands that bind to these receptors include light-sensitive compounds, odors, hormones, and neurotransmitters. The ligands for G-protein linked receptors come in different sizes, from small molecules to large proteins. G protein-coupled receptors are involved in many diseases, but are also the target of around half of all modern medicinal drugs.
The process of how a G-protein linked receptor works is outlined in Figure above.
| A. | A ligand such as a hormone (small, purple molecule) binds to the G-linked receptor (red molecule). Before ligand binding, the inactive G-protein (yellow molecule) has GDP bound to it. |
| B. | The receptor changes shape and activates the G-protein and a molecule of GTP replaces the GDP. |
| C. | The G-protein moves across the membrane then binds to and activates the enzyme (green molecule). This then triggers the next step in the pathway to the cell's response. After activating the enzyme, the G-protein returns to its original position. The second messenger of this signal transduction is cAMP, as shown in C. |
The sensing of the external and internal environments at the cellular level relies on signal transduction. Defects in signal transduction pathways can contribute or lead to many diseases, including cancer and heart disease. This highlights the importance of signal transductions to biology and medicine.
In response to a signal, a cell may change activities in the cytoplasm or in the nucleus that include the switching on or off of genes. Changes in metabolism, continued growth, movement, or death are some of the cellular responses to signals that require signal transduction.
Gene activation leads to other effects, since the protein products of many of the responding genes include enzymes and factors that increase gene expression. Gene expression factors produced as a result of a cascade can turn on even more genes. Therefore one stimulus can trigger the expression of many genes, and this in turn can lead to the activation of many complex events. In a multicellular organism these events include the increased uptake of glucose from the blood stream (stimulated by insulin), and the movement of neutrophils to sites of infection (stimulated by bacterial products). The set of genes and the order in which they are activated in response to stimuli are often called a genetic program.
Figure 3.37
Next we turn our attention to photosynthesis.