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Exocytosis (/ ˌ ɛ k s oʊ s aɪ ˈ t oʊ s ɪ s / [1] [2]) is a form of active transport and bulk transport in which a cell transports molecules (e.g., neurotransmitters and proteins) out of the cell (exo-+ cytosis). As an active transport mechanism, exocytosis requires the use of energy to transport material.
Exocytosis (L) and Endocytosis (R) Exocytosis is when a cell directs the contents of secretory vesicles out of the cell membrane. The vesicles fuse with the cell membrane and their content, usually protein, is released out of the cell. There are two types of exocytosis: Constitutive secretion and Regulated secretion.
In phagocytosis, involving the destruction of pathogens, the pathogens are surrounded and then engulfed through endocytosis. The vacuole then forms and closes around the pathogens. In exocytosis, the lysosome and vacuole fuse together which allows enzymes to destroy pathogens. Debris from the pathogens is then released from the cell.
The 2013 Nobel Prize in Physiology or Medicine was shared by James Rothman, Randy Schekman and Thomas Südhof for their roles in elucidating (building upon earlier research, some of it by their mentors) the makeup and function of cell vesicles, especially in yeasts and in humans, including information on each vesicle's parts and how they are assembled.
Exocytosis is the process by which a large amount of molecules are released; thus it is a form of bulk transport. Exocytosis occurs via secretory portals at the cell plasma membrane called porosomes. Porosomes are permanent cup-shaped lipoprotein structures at the cell plasma membrane, where secretory vesicles transiently dock and fuse to ...
Axon terminals are specialized to release neurotransmitters very rapidly by exocytosis. [1] Neurotransmitter molecules are packaged into synaptic vesicles that cluster beneath the axon terminal membrane on the presynaptic side (A) of a synapse.
Schematic drawing illustrating clathrin-mediated (left) and clathrin-independent endocytosis (right) of synaptic vesicle membranes. Endocytosis pathways can be subdivided into four categories: namely, receptor-mediated endocytosis (also known as clathrin-mediated endocytosis), caveolae, pinocytosis, and phagocytosis.
Eventually, there is vesicle fusion with the cell membrane at porosomes, by a process called exocytosis, dumping its contents out of the cell's environment. [2] Strict biochemical control is maintained over this sequence by usage of a pH gradient: the pH of the cytosol is 7.4, the ER's pH is 7.0, and the cis-golgi has a pH of 6.5.