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postsynaptic neurotransmitter receptor diffusion trapping

Definition

Target type: biologicalprocess

The process by which diffusing neurotransmitter receptor becomes trapped at the postsynaptic specialization membrane. This is typically due to interaction with components of the post-synaptic specialization. [PMID:18832033]

Postsynaptic neurotransmitter receptor diffusion trapping is a crucial mechanism in synaptic plasticity and neuronal communication. It involves the lateral diffusion of neurotransmitter receptors within the postsynaptic membrane, where they can be trapped by specific interactions with scaffolding proteins or other components of the postsynaptic density (PSD). This trapping enhances the local concentration of receptors at the synapse, amplifying the effects of neurotransmitter release and facilitating signal transduction.

Here's a detailed breakdown of the process:

1. **Diffusion:** Neurotransmitter receptors, primarily ionotropic and metabotropic receptors, are embedded in the lipid bilayer of the postsynaptic membrane. These receptors are highly mobile and undergo lateral diffusion within the membrane, constantly moving in random directions.

2. **Trapping by Scaffolding Proteins:** The PSD, a dense protein structure located beneath the postsynaptic membrane, provides a scaffold for the organization of various signaling molecules, including neurotransmitter receptors. Specific scaffolding proteins, like PSD-95, gephyrin, and SAP97, bind to the intracellular domains of neurotransmitter receptors. These interactions effectively trap the receptors within the PSD, preventing their free diffusion away from the synapse.

3. **Clustering and Local Concentration:** The trapping of receptors by scaffolding proteins leads to the formation of receptor clusters within the PSD. This clustering increases the local concentration of receptors at the synapse, enhancing their sensitivity to neurotransmitter release.

4. **Signal Amplification:** The increased concentration of receptors at the synapse amplifies the signal transduction pathways initiated by neurotransmitter binding. This is particularly important for the activation of downstream signaling cascades and the induction of long-term synaptic plasticity.

5. **Regulation and Dynamics:** Diffusion trapping is not a static process. It is dynamically regulated by various factors, including:
- **Synaptic activity:** Increased neurotransmitter release can trigger the phosphorylation of scaffolding proteins, leading to enhanced receptor trapping.
- **Cellular signaling pathways:** Second messenger systems, such as cAMP and Ca2+, can modulate the interaction between receptors and scaffolding proteins.
- **Internalization and degradation:** Trapped receptors can be internalized from the PSD and degraded, providing a mechanism for regulating receptor number and sensitivity.

6. **Implications for Synaptic Plasticity:** Diffusion trapping plays a critical role in synaptic plasticity, the ability of synapses to strengthen or weaken over time. By controlling the local concentration of receptors, this mechanism contributes to the long-lasting changes in synaptic efficacy that underlie learning and memory.

In summary, postsynaptic neurotransmitter receptor diffusion trapping is a sophisticated mechanism that regulates receptor distribution and enhances signal transduction at synapses. It plays a vital role in synaptic plasticity, neuronal communication, and cognitive function.'
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Proteins (7)

ProteinDefinitionTaxonomy
Voltage-dependent calcium channel gamma-4 subunitA voltage-dependent calcium channel gamma-4 subunit that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q9UBN1]Homo sapiens (human)
Voltage-dependent calcium channel gamma-3 subunitA voltage-dependent calcium channel gamma-3 subunit that is encoded in the genome of human. [PRO:DNx, UniProtKB:O60359]Homo sapiens (human)
Disks large homolog 4A disks large homolog 4 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P78352]Homo sapiens (human)
Voltage-dependent calcium channel gamma-2 subunitA voltage-dependent calcium channel gamma-2 subunit that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q9Y698]Homo sapiens (human)
Voltage-dependent calcium channel gamma-7 subunitA voltage-dependent calcium channel gamma-7 subunit that is encoded in the genome of human. [PRO:DNx, UniProtKB:P62955]Homo sapiens (human)
Voltage-dependent calcium channel gamma-8 subunitA voltage-dependent calcium channel gamma-8 subunit that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q8WXS5]Homo sapiens (human)
Voltage-dependent calcium channel gamma-5 subunitA voltage-dependent calcium channel gamma-5 subunit that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q9UF02]Homo sapiens (human)

Compounds (4)

CompoundDefinitionClassesRoles
tacrinetacrine : A member of the class of acridines that is 1,2,3,4-tetrahydroacridine substituted by an amino group at position 9. It is used in the treatment of Alzheimer's disease.

Tacrine: A cholinesterase inhibitor that crosses the blood-brain barrier. Tacrine has been used to counter the effects of muscle relaxants, as a respiratory stimulant, and in the treatment of Alzheimer's disease and other central nervous system disorders.
acridines;
aromatic amine
EC 3.1.1.7 (acetylcholinesterase) inhibitor
nimodipinenimodipine : A dihydropyridine that is 1,4-dihydropyridine which is substituted by methyl groups at positions 2 and 6, a (2-methoxyethoxy)carbonyl group at position 3, a m-nitrophenyl group at position 4, and an isopropoxycarbonyl group at position 5. An L-type calcium channel blocker, it acts particularly on cerebral circulation, and is used both orally and intravenously for the prevention and treatment of subarachnoid hemorrhage from ruptured intracranial aneurysm.

Nimodipine: A calcium channel blockader with preferential cerebrovascular activity. It has marked cerebrovascular dilating effects and lowers blood pressure.
2-methoxyethyl ester;
C-nitro compound;
dicarboxylic acids and O-substituted derivatives;
diester;
dihydropyridine;
isopropyl ester
antihypertensive agent;
calcium channel blocker;
cardiovascular drug;
vasodilator agent
ith 4012
tat-nr2b9cTat-NR2B9c: a synthetic peptide consisting of the C-terminal 9 amino acids of the NR2B subunit of the NMDA receptor fused to the cell membrane protein transduction domain of the HIV-1-Tat protein