Page last updated: 2024-10-24

trans-synaptic signaling

Definition

Target type: biologicalprocess

Cell-cell signaling in either direction across the synaptic cleft. [GOC:dos]

Trans-synaptic signaling refers to the communication between neurons that occurs across the synaptic cleft, the small gap separating the presynaptic and postsynaptic neurons. This intricate process enables the transmission of information between neurons, driving a wide range of physiological functions.

Here's a detailed breakdown of the steps involved:

1. **Presynaptic Neuron:** The signaling process begins in the presynaptic neuron, which synthesizes and stores neurotransmitters, chemical messengers responsible for transmitting signals across the synapse. These neurotransmitters are packaged into vesicles, tiny membrane-bound sacs that reside within the presynaptic terminal, the specialized structure at the end of the presynaptic axon.

2. **Action Potential Arrival:** When an action potential, a brief electrical signal, travels down the presynaptic axon and reaches the terminal, it triggers a cascade of events that lead to the release of neurotransmitters. Voltage-gated calcium channels open, allowing calcium ions to flow into the presynaptic terminal.

3. **Neurotransmitter Release:** The influx of calcium ions initiates a complex series of protein interactions that cause the synaptic vesicles to fuse with the presynaptic membrane. This fusion event releases the neurotransmitters into the synaptic cleft, the space between the presynaptic and postsynaptic neurons.

4. **Neurotransmitter Binding:** The released neurotransmitters diffuse across the synaptic cleft and bind to specific receptors located on the postsynaptic membrane of the receiving neuron. These receptors are highly specialized proteins designed to recognize and bind to specific neurotransmitters.

5. **Postsynaptic Signaling:** The binding of neurotransmitters to their receptors triggers a series of events in the postsynaptic neuron, leading to changes in its membrane potential or intracellular signaling pathways. This can involve the opening or closing of ion channels, leading to depolarization or hyperpolarization of the postsynaptic membrane, or the activation of intracellular signaling cascades that modify gene expression or protein activity.

6. **Neurotransmitter Removal:** To ensure precise and efficient signaling, the neurotransmitters must be removed from the synaptic cleft. This is achieved through several mechanisms, including reuptake by the presynaptic neuron, enzymatic degradation in the synaptic cleft, or diffusion away from the synapse.

7. **Trans-synaptic Signaling Variability:** The specific neurotransmitters involved, the types of receptors present, and the strength of the synaptic connection can all vary, resulting in diverse forms of trans-synaptic signaling. This diversity is crucial for the complex information processing capabilities of the nervous system.

8. **Synaptic Plasticity:** The strength and efficacy of synaptic connections are not fixed but can be modified over time. This process, known as synaptic plasticity, underlies learning and memory formation. Synaptic plasticity can occur through various mechanisms, including changes in the number of receptors, the efficiency of neurotransmitter release, and the structure of the synapse.

9. **Types of Synapses:** Trans-synaptic signaling can occur at various types of synapses. Chemical synapses, the most common type, rely on the release of neurotransmitters. Electrical synapses, on the other hand, allow direct flow of electrical current between neurons through gap junctions, providing rapid and synchronized communication.

Trans-synaptic signaling is a fundamental process in the nervous system, enabling communication between neurons and orchestrating a vast array of physiological functions, from sensory perception and motor control to cognitive processes and emotional responses. The intricate interplay of neurotransmitters, receptors, and signaling pathways at synapses forms the basis for neural computation and information processing in the brain.'
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Proteins (1)

ProteinDefinitionTaxonomy
Receptor-type tyrosine-protein phosphatase SA receptor-type tyrosine-protein phosphatase S that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q13332]Homo sapiens (human)

Compounds (4)

CompoundDefinitionClassesRoles
baicaleintrihydroxyflavoneangiogenesis inhibitor;
anti-inflammatory agent;
antibacterial agent;
anticoronaviral agent;
antifungal agent;
antineoplastic agent;
antioxidant;
apoptosis inducer;
EC 1.13.11.31 (arachidonate 12-lipoxygenase) inhibitor;
EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor;
EC 3.4.21.26 (prolyl oligopeptidase) inhibitor;
EC 3.4.22.69 (SARS coronavirus main proteinase) inhibitor;
EC 4.1.1.17 (ornithine decarboxylase) inhibitor;
ferroptosis inhibitor;
geroprotector;
hormone antagonist;
plant metabolite;
prostaglandin antagonist;
radical scavenger
morinmorin : A pentahydroxyflavone that is 7-hydroxyflavonol bearing three additional hydroxy substituents at positions 2' 4' and 5.

morin: a light yellowish pigment found in the wood of old fustic (Chlorophora tinctoria)
7-hydroxyflavonol;
pentahydroxyflavone
angiogenesis modulating agent;
anti-inflammatory agent;
antibacterial agent;
antihypertensive agent;
antineoplastic agent;
antioxidant;
EC 5.99.1.2 (DNA topoisomerase) inhibitor;
hepatoprotective agent;
metabolite;
neuroprotective agent
scutellareinscutellarein : Flavone substituted with hydroxy groups at C-4', -5, -6 and -7.

scutellarein: aglycone of scutellarin from Scutellaria baicalensis; carthamidin is 2S isomer of scutellarein; do not confuse with isoscutellarein and/or isocarthamidin which are respective regioisomers, or with the scutelarin protein
tetrahydroxyflavonemetabolite
tricetintricetin : Flavone hydroxylated at positions 3', 4', 5, 5' and 7.pentahydroxyflavoneantineoplastic agent;
metabolite