It has been suggested that this article or section be merged into Endocytosis. (Discuss)

Most animal cells take up portions of their surface plasma membranes in a process called endocytosis. The main route of endocytosis is the coated pit which buds into a cell to form a cytoplasmic vesicle — a clathrin-coated vesicle. The membrane so internalised is processed in a series of intracellular organelles which include endosomes and lysosomes. Some of this membrane, maybe most of it, is returned to the cell surface by a process which is almost the opposite of endocytosis: this is called exocytosis. The whole cycle of endocytosis plus exocytosis is known as the endocytic cycle. Wikipedia does not have an article with this exact name. ... It has been suggested that Endocytic cycle be merged into this article or section. ... Drawing of a cell membrane A component of every biological cell, the cell membrane (or plasma membrane) is a thin and structured bilayer of phospholipid and protein molecules that envelopes the cell. ... It has been suggested that Endocytic cycle be merged into this article or section. ... Clathrin coat structure Clathrin is a protein that is the major constituent of the coat of the clathrin coated pits and coated vesicles formed during endocytosis of materials at the surface of cells. ... In biology an endosome is an endocytotic vesicle derived from the plasma membrane. ... Lysosomes are organelles in eukaryotic cells that contain digestive enzymes to digest macromolecules. ... This page is currently under construction. ...

The endocytic cycle is crucial for the well-being of individual cells and multicellular organisms. A few examples follow:

LDL metabolism

Low density lipoprotein (LDL) originates in the liver and is transported around an animal by the blood stream. From there it is taken up by other cells, such as fibroblasts, and degraded: this provides a source of cholesterol for the growth of these other cells. LDL in the blood binds to LDL receptors on the surface of fibroblasts; these receptors concentrate in coated pits (they are about 200x as concentrated here as along the rest of the cell’s plasma membrane) and are internalised when the pit becomes a coated vesicle. The itinerary of the LDL receptor inside the cell is complex, but it spends little time there. Within a fraction of a minute it has released its LDL cargo and is returned to the cell surface by exocytosis. It is now ready for another round of LDL clearance. Low-density lipoprotein (LDL) refers to a class and range of lipoprotein particles, varying somewhat in their size and contents, which carry cholesterol in the blood and around the body, for use by various cells. ... Low-density lipoprotein (LDL) refers to a class and range of lipoprotein particles, varying somewhat in their size and contents, which carry cholesterol in the blood and around the body, for use by various cells. ... A fibroblast is a cell that makes the structural fibers and ground substance of connective tissue. ... Cholesterol is a sterol (a combination steroid and alcohol), a lipid found in the cell membranes of all body tissues, and is transported in the blood plasma of all animals. ... Brown and Goldstein won a Nobel Prize for their identification of the Low Density Lipoprotein (LDL) receptor 30 years ago whilst they were studying the disease familiar hypercholesterolaemia. ...

High levels of LDL in the blood are observed in atherosclerosis and associated with the disease; the endocytic cycle reduces LDL through consuming it. This may or may not be useful in regulating increased levels of LDL, although it may have limitations, or not increase at all in the presence of extra LDL molecules.

Transferrin receptor

Transferrin is a plasma protein which is able to combine with iron ions: it is the vehicle with which iron is carried around the body. Free ferric ions are toxic; but cells need iron to build many of their proteins including cytochromes and hemoglobin. Ferric ions are carried in the blood tightly bound to transferrin as ferritransferrin. Dividing cells, which need the iron, gain it by binding the ferritransferrin to transferrin receptors on their surfaces. These receptors also have a high affinity for coated pits. Like the LDL receptor, the transferrin receptor is internalised into a coated vesicle. The iron is released inside the cell and the receptor returned to the cell surface. The route this receptor takes inside the cell appears to be different from that taken by the LDL receptor, because it takes about 10 minutes before it is exocytosed. Transferrin receptor is a carrier protein for transferrin. ... Transferrin is a plasma protein for iron ion delivery. ... Cytochromes are generally membrane-bound proteins that contain heme groups and carry out electron transport. ... Structure of hemoglobin. ...

Synapse function

Impulses between neurons are transmitted by the release of neurotransmitters at the junction between the two cells, a region called a synapse. This release is effected by exocytosis at the presynaptic terminal. A vesicle full of transmitter, acetylcholine (for example), in the presynaptic terminal fuses with its neighbouring plasma membrane and thereby releases a burst of acetylcholine into the synaptic space. The acetylcholine is rapidly degraded here, but before this happens it activates acetylcholine receptors on the postsynaptic terminal and triggers an electrical impulse in that cell. The membrane added to the presynaptic terminal is recovered by endocytosis and recycled to form fresh vesicles full of neurotransmitter, ready for another cycle of postsynaptic excitation. Illustration of the major elements in a prototypical synapse. ... Neurons (also called nerve cells) are the primary cells of the nervous system. ... Neurotransmitters are chemicals that are used to relay, amplify and modulate electrical signals between a presynaptic and a postsynaptic neuron. ... In a synapse between two neurons, the cell that releases the neurotransmitter is referred to as the presynaptic cell. ... The chemical compound acetylcholine, often abbreviated as ACh, was the first neurotransmitter to be identified. ... An acetylcholine receptor (abbreviated AChR) is an integral membrane protein that responds to the binding of the neurotransmitter acetylcholine by opening a pathway in the membrane for the diffusion of ions across the cell membrane. ...

The function of the nervous system is thus dependent on this endocytic cycle. A nice example of this dependence is found in fruit flies. A key protein required for endocytosis is dynamin: it assists in budding a coated pit into a cell to form a coated vesicle. Mutations in the dynamin gene exist in which the activity of the dynamin protein is lost at above-normal temperatures (for the fly): these are called temperature sensitive mutations. Such mutant flies have the property that, when the fly is brought from its normal 22ºC to 30ºC, the dynamin function is lost: however, when the flies are cooled to 22ºC, it is regained. In other words, in these mutant flies, the endocytic cycle can be turned off at 30ºC, and turned back on by cooling. What one observes is that, within seconds of warming to 30ºC, the fruit flies become paralysed: they drop out of the air and appear near-dead. On cooling, they slowly get up, flutter their wings and fly away. The endocytic cycle has been temporarily suspended with drastic effects! Dynamin is a GTPase thought to be responsible for endocytosis in the eukaryotic cell, and is involved in vesicle (biology) trafficking both at the cell surface (particularly caveolae internalization) as well as at the Golgi (1)(2)(4). ... This article is about mutation in biology, for other meanings see: mutation (disambiguation). ...

Non-polarised and polarised endocytic cycles

Non-polarised cells

Animal cells, such as fibroblasts, as grown in culture in the laboratory are usually stationary; they grow and divide, but rarely move about. They have a normal endocytic cycle: coated pits 'bud in' from all over the cell’s surface in a random fashion and the returned membrane is exocytosed at the cell’s surface, also at random.

Polarised cells

Moving cells, such as fibroblasts, are arranged quite differently. Endocytosis by coated pits occurs, as in stationary cells, at random. But in motile cells exocytosis now occurs at the front of the cell: it is here that both LDL- and transferrin-receptors emerge from inside the cell and return to the cell surface. As the sites of endocytosis (at random on the cell surface) and exocytosis (at the front edge of the cell) are separated in space, it follows that (within the cell’s context) there is a flow of membrane from the front rearwards.

The consequences of this polarised endocytic cycle are profound:

• The membrane added at the front of the cell is believed to provide the surface there for the cell to extend itself forward as it moves.

Image File history File links No higher resolution available. ...

• Evidence indicates that those molecules in the cell’s surface which act as the feet of the cell — the integrins which attach the cell to the substratum — can also be endocytosed and transported through the cell. In this way fresh adhesion sites (see cell adhesion) are provided at the cell’s front. An integrin, or integrin receptor, is an integral membrane protein in the plasma membrane of cells. ... Schematic of cell adhesion The study of cell adhesion is part of cell biology. ...

• The flow of membrane from the front rearwards is not a flow of average plasma membrane proteins: the membrane internalised is a subset of plasma membrane proteins, such as LDL or transferrin receptors and the lipid bilayer in which they sit. These recycling molecules appear at the front surface of the cell and diffuse about, drifting rearwards until they are recaptured by a coated pit and transported back, through the cell, to the front. Other proteins do not participate in this cycle: therefore, they experience a slow rearward flow of the lipid bilayer in which they reside. They are thus subject to two different influences: (a) they tend to get swept backwards in this lipid flow and (b) they tend to randomise their distribution on the cell surface by Brownian motion. Calculation shows that, for non-cycling proteins, diffusion is the more important influence, so these molecules would be expected to have a near-random distribution on the cell’s surface. However, if a large object were attached to the cell surface which was unable to diffuse against the flow, it would be expected to be swept backwards by the flow towards the trailing end of the cell. Indeed, it would act as a marker for that flow. This is the reason why carbon particles attached to the dorsal surface of a moving cell, or why aggregates of surface proteins, are seen to move to the back of a cell. This process is known as cap formation. Three different views of Brownian motion, with 32 steps, 256 steps, and 2048 steps denoted by progressively lighter colors. ... There are very few or no other articles that link to this one. ...

Further support for this scheme comes from a study of yeast cells (S. cerevisiae) which undergo a primitive form of movement called shmooing. A protein which cycles rapidly would be expected to be most concentrated near the shmoo tip of such a cell , whereas a non-cycling protein would be expected to be swept backwards slightly. Both these distributions have been observed for a cycling and non-cycling variant of the same protein in the plasma membrane of yeast cells as they shmoo. Binomial name Saccharomyces cerevisiae Meyen ex E.C. Hansen Saccharomyces cerevisiae is a species of budding yeast. ...

• The molecular feet of a cell (usually integrins), when bound to the substratum, cannot diffuse about. Like any other macroscopic object sitting in the lipid flow, they are thus pushed backwards. However, they cannot move backwards (they are attached to the fixed substratum)) and therefore push the cell forward. This may be the force against the substratum which enables a cell to move forward.

• Polarised endocytic cycles are believed to exist in other cellular contexts but the evidence for them at present is less clear.