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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.
There are two types of exocytosis: Constitutive secretion and Regulated secretion. In both of these types, a vesicle buds from the Golgi Apparatus and is shuttled to the plasma membrane, to be exocytosed from cell. Exocytosis of lysosomes commonly serves to repair damaged areas of the plasma membrane by replenishing the lipid bilayer. [5]
When a vesicle is produced inside the cell and fuses with the plasma membrane to release its contents into the extracellular space, this process is known as exocytosis. In the reverse process, a region of the cell membrane will dimple inwards and eventually pinch off, enclosing a portion of the extracellular fluid to transport it into the cell.
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 ...
Exocytosis is infiltration of the epidermis by inflammatory or circulating blood cells. [1] See also. Skin lesion; Skin disease; List of skin diseases; References
When an action potential propagates down the motor neuron axon and arrives at the axon terminal, it causes a depolarization of the axon terminal and opens calcium channels. This causes the release of the neurotransmitters via vesicle exocytosis. After exocytosis, vesicles are recycled during a process known as the synaptic vesicle cycle.
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Consequently, exocytosis releases acetylcholine in packets that are called quanta. The acetylcholine quantum diffuses through the acetylcholinesterase meshwork, where the high local transmitter concentration occupies all of the binding sites on the enzyme in its path.