Target type: biologicalprocess
The process in which a neuronal cell in a multicellular organism interprets its surroundings. [GOC:go_curators]
Neuron recognition is a complex and multifaceted process that involves the coordinated interaction of various molecular cues and cellular mechanisms. It encompasses the ability of neurons to identify and interact with their appropriate target cells, establishing precise and functional neuronal circuits within the nervous system.
The process of neuron recognition can be broadly divided into two phases:
1. **Axon guidance:** This initial phase involves the directed growth of axons, the long projections of neurons, towards their target cells. Axon guidance relies on a series of molecular signals, including chemoattractants and chemorepellents, which act as guiding cues for growing axons. These signals can be secreted from target cells or present on the surface of other cells or extracellular matrix components. Axon guidance is a highly dynamic process, involving a delicate balance of attractive and repulsive cues that direct axons along specific pathways.
2. **Synapse formation:** Once an axon reaches its target cell, the second phase of neuron recognition involves the establishment of a specialized communication point called a synapse. Synapse formation requires the precise apposition of the presynaptic axon terminal with the postsynaptic target cell. This process is regulated by a cascade of molecular interactions, including adhesion molecules, cell surface receptors, and signaling pathways. Synaptic specificity ensures that the right neurons connect with each other, forming functional circuits that underlie various brain functions.
The molecular mechanisms underlying neuron recognition are highly intricate and involve a wide range of signaling molecules and cellular processes. Some of the key players in neuron recognition include:
- **Netrins:** These are chemoattractants that guide axons towards their targets. They interact with specific receptors on the surface of axons, triggering signaling cascades that promote axonal growth.
- **Slit proteins:** These act as chemorepellents, repelling axons from specific regions. They bind to Robo receptors on axons, inhibiting axonal growth and directing axons towards alternative pathways.
- **Ephrins and Eph receptors:** These are a family of cell surface molecules that mediate both attractive and repulsive axon guidance. They interact in a bi-directional manner, influencing both the growth of axons and the development of target cells.
- **Cadherins:** These are cell adhesion molecules that play a crucial role in synapse formation. They mediate the adherence of presynaptic and postsynaptic membranes, promoting the stabilization of synapses.
- **Neurotrophins:** These are growth factors that promote the survival and differentiation of neurons. They act as chemoattractants, guiding axons towards their targets and supporting the establishment of functional synapses.
The precise molecular mechanisms of neuron recognition vary depending on the specific type of neurons and their target cells. Moreover, neuron recognition is a highly dynamic process that is influenced by various factors, including the developmental stage, the environment, and the presence of other cells.
Disruptions in neuron recognition can lead to a variety of neurological disorders, including developmental disabilities, neurodegenerative diseases, and mental health problems. Therefore, understanding the molecular mechanisms underlying neuron recognition is crucial for developing novel therapeutic strategies for these conditions.
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Protein | Definition | Taxonomy |
---|---|---|
C-X-C chemokine receptor type 4 | A C-X-C chemokine receptor type 4 that is encoded in the genome of human. [PRO:WCB, UniProtKB:P61073] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
zalcitabine | zalcitabine : A pyrimidine 2',3'-dideoxyribonucleoside compound having cytosine as the nucleobase. Zalcitabine: A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by a hydrogen. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. The compound is a potent inhibitor of HIV replication at low concentrations, acting as a chain-terminator of viral DNA by binding to reverse transcriptase. Its principal toxic side effect is axonal degeneration resulting in peripheral neuropathy. | pyrimidine 2',3'-dideoxyribonucleoside | antimetabolite; antiviral drug; HIV-1 reverse transcriptase inhibitor |
plerixafor | plerixafor : An azamacrocycle consisting of two cyclam rings connected by a 1,4-phenylenebis(methylene) linker. It is a CXCR4 chemokine receptor antagonist and a hematopoietic stem cell mobilizer. It is used in combination with grulocyte-colony stimulating factor (G-CSF) to mobilize hematopoietic stem cells to the perpheral blood for collection and subsequent autologous transplantation in patients with non-Hodgkin's lymphoma and multiple myeloma. plerixafor: a bicyclam derivate, highly potent & selective inhibitor of HIV-1 & HIV-2 | azacycloalkane; azamacrocycle; benzenes; crown amine; secondary amino compound; tertiary amino compound | anti-HIV agent; antineoplastic agent; C-X-C chemokine receptor type 4 antagonist; immunological adjuvant |
benzylaniline | benzylaniline: major metabolite of antazoline; RN given refers to parent cpd | ||
terephthalamide | benzenedicarboxamide | ||
krh 1636 | KRH 1636: structure in first source | ||
amd 8664 | |||
cyclo(d-tyrosyl-arginyl-arginyl-3-(2-naphthyl)alanyl-glycyl) | oligopeptide | ||
amd 070 | mavorixafor: a derivative of AMD3100; a CXCR4 blocker | aminoquinoline | |
wz 811 | |||
tn14003 | TN14003: synthetic antagonist 14-mer peptide inhibiting metastasis in an animal model |