Clathrin-coated pits/vesicles

Clathrin-coated Pits Clathrin-coated Vesicle CLC... 

In the classic model of synaptic vesicle recycling in nerve terminals, synaptic vesicles fuse completely with the plasma membrane and the integrated vesicle proteins move away from the active zone to adjacent membrane regions (Fig. 9-9A). In these regions, clathrin-mediated synaptic vesicle endocytosis takes place rapidly after neurotransmitter release (within seconds) [64]. The process starts with the formation of a clathrin-coated pit that invaginates toward the interior of the cell and pinches off to form a clathrin-coated vesicle [83]. Coated vesicles are transient organelles that rapidly shed their coats in an ATP/chaperone dependent process. Once uncoated, the recycled vesicle fuses with a local EE for reconstitution as a synaptic vesicle. Subsequently, the recycled synaptic vesicle is filled with neurotransmitter and it returns to the release site ready for use. This may be the normal pathway when neurotransmitter release rates are modest. Clathrin/ EE-based pathways become essential when synaptic proteins have been incorporated into the presynaptic plasma membrane. 

Both intracellular depletion of potassium and hypertonic treatment lead to disruption of clathrin from the inner side of the plasma membrane. Consequently, the formation of clathrin-coated pits and clathrin-coated vesicles is... 

For the formation of clathrin-coated vesicles, several proteins are required. Currently, there are several recombinant inhibitors available, which block different steps of coated pit/vesicle formation for example, amphiphysin (53), clathrin assembly protein AP180 (54), epsin (55), and clathrin mutant (56). 

Some bacteria glide with a twitching movement induced by rapid retraction of pili.340 Another type of movement involves the pinching off of vesicles, e.g., of clathrin-coated pits (Fig. 8-27). This is a GTP-driven process that requires a mechanoenzyme called dynamin, 341-342... 

Receptor-mediated endocytosis is the selective uptake of extracellular macromolecules (such as cholesterol) through their binding to specific cell-surface receptors. The receptor-macromolecule complex then accumulates in clathrin-coated pits and is endocytosed via a clathrin-coated vesicle. 

Both endocytosis of material at the plasma membrane and exocytosis from the Golgi apparatus involve the formation of clathrin-coated pits and vesicles. On the cytosolic side of the membrane these structures have an electron-dense coat consisting mainly of the protein clathrin, the polypeptides of which form a three-legged structure known as a triskelion. The clathrin triskelions assemble into a basket-like convex framework that causes the membrane to invaginate at that point and eventually to pinch off and form a vesicle. In endocytosis these clathrin-coated vesicles migrate into the cell where the clathrin coats are lost before delivering their contents to the lysosomes. 

Fig. 3. Receptor-mediated endocytosis involves clathrin-coated pits and vesicles.

Gene delivery systems can distribute plasmids to the desired target cells, after which the plasmid is internalized into the cell by a number of mechanisms, such as adsorptive endocytosis, receptor-mediated endocytosis, micropinocytosis, caveolae-mediated endocytosis and phagocytosis (see Section 1.3.3.2). The intracellular fate of plasmids depends on the means by which they are internalized and translocated to the cytoplasms and then to the nucleus. In coated-pit endocytosis, DNA complexes first bind to the cell surface, then migrate to clathrin-coated pits about 150 ran in diameter and are internalized from the plasma membrane to form coated vesicles. 

Non-clathrin-coated pit internalization can occur through smooth imagination of 150-300 nm vesicles or via potocytosis. This pathway has been shown to be involved in the transport of folate and other small molecules into the cytoplasm. Plasmids are taken up by muscles through the T-tubules system and caveolae via potocytosis. Muscle cells appear to take up plasmids through the T-tubule system and caveolae via potocytosis. Apart from coated or uncoated pit pathways, cells may also take up plasmid/cationic carrier complexes via plasma membrane destabilization. Particles greater than 200 nm in diameter are not... 

The rate of protein clearance has been estimated as 10% of the rate of fluid clearance from alveoli [173]. IgG clearance is probably mediated by FcRn transcytosis in distal type I alveolar epithelium and more proximal bronchial epithelium. Type I alveolar epithelium and bronchial epithelium contain the necessary subcellular structures for FcRn-mediated transcytosis vesicles, membrane invaginations, caveolae, and clathrin-coated pits [173,174], FcRn mRNA is expressed in lung although the cell types and locations have not yet been determined [112], Moreover, primary alveolar epithelial monolayer cell cultures express functional FcRn [173], plgA-R/SC transcytosis is thought to contribute little to distal (alveolar) airway IgG transport but might mediate more proximal (bronchial or bronchiolar) IgA transport [173], Uptake of an aerosolized IgG Fc-erythropoietin fusion molecule and subsequent erythropoietin-induced reticulocytosis has been demonstrated in human and nonhuman primates [175],... 

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