Page last updated: 2024-10-24

regulation of synaptic vesicle budding from presynaptic endocytic zone membrane

Definition

Target type: biologicalprocess

Any process that modulates the frequency, rate or extent of synaptic vesicle budding from presynaptic endocytic zone membrane. [GOC:dos]

Synaptic vesicle budding from the presynaptic endocytic zone membrane is a complex and tightly regulated process that ensures the efficient recycling of synaptic vesicles for neurotransmitter release. Here's a detailed description of the biological process:

1. **Triggering of Endocytosis:** After neurotransmitter release, the fusion of synaptic vesicles with the presynaptic plasma membrane leaves behind a patch of membrane called the endocytic zone. This zone becomes the site of new vesicle formation. The process is triggered by the arrival of a new action potential and the subsequent influx of calcium ions into the presynaptic terminal.

2. **Clathrin-Mediated Budding:** The formation of new synaptic vesicles begins with the recruitment of clathrin, a protein that forms a cage-like structure around the endocytic zone membrane. Clathrin assembly is initiated by adaptor proteins, such as AP-2, which bind to specific phosphoinositides (PIP2) on the membrane and interact with clathrin. These interactions lead to the formation of a clathrin-coated pit.

3. **Dynamin-Mediated Fission:** As the clathrin coat assembles, the pit progressively invaginates, forming a bud. The neck of the bud is then constricted by the GTPase dynamin, which forms a ring-like structure around the neck. Dynamin hydrolyzes GTP, leading to a conformational change that constricts the neck and ultimately severs the bud from the plasma membrane.

4. **Uncoating and Recycling:** Once the vesicle is fully formed, the clathrin coat is disassembled by proteins like Hsc70 and auxilin. The newly formed vesicle is then transported to the reserve pool of synaptic vesicles, which are located away from the active zone. The vesicle membrane is then recycled through a series of steps, which may involve endosomes and other membrane compartments.

5. **Regulation of Endocytosis:** The entire process of synaptic vesicle budding is tightly regulated by various factors, including:

* **Calcium concentration:** Calcium influx, triggered by the action potential, activates key proteins involved in endocytosis, including AP-2 and dynamin.
* **Phosphorylation:** Proteins involved in endocytosis can be phosphorylated, modifying their activity and influencing the rate of vesicle budding.
* **Lipid composition:** The composition of lipids in the presynaptic membrane can affect the formation of clathrin-coated pits and the efficiency of endocytosis.
* **Cytoskeleton:** The cytoskeleton, particularly actin filaments, plays a role in the positioning and movement of endocytic zones and the newly formed vesicles.

6. **Importance of Endocytosis:** Efficient synaptic vesicle budding is crucial for maintaining neurotransmission. Recycling of synaptic vesicle membrane ensures a continuous supply of vesicles for neurotransmitter release, allowing for rapid and sustained signaling at synapses. Disruptions in this process can lead to neurotransmitter depletion and impaired synaptic function, contributing to various neurological disorders.'
"

Proteins (1)

ProteinDefinitionTaxonomy
Solute carrier family 2, facilitated glucose transporter member 4A solute carrier family 2, facilitated glucose transporter member 4 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P14672]Homo sapiens (human)

Compounds (2)

CompoundDefinitionClassesRoles
cytochalasin bcytochalasin B : An organic heterotricyclic compound, that is a mycotoxin which is cell permeable an an inhibitor of cytoplasmic division by blocking the formation of contractile microfilaments.

Cytochalasin B: A cytotoxic member of the CYTOCHALASINS.
cytochalasin;
lactam;
lactone;
organic heterotricyclic compound
actin polymerisation inhibitor;
metabolite;
mycotoxin;
platelet aggregation inhibitor
wzb117WZB117: structure in first source