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衔接蛋白反应调节剂通过改变其磷酸化状态来调节神经元的发育和可塑性。

Collapsin response mediator proteins regulate neuronal development and plasticity by switching their phosphorylation status.

机构信息

Department of Molecular Pharmacology and Neurobiology, Yokohama City University Graduate School of Medicine, Fuku-ura 3-9, Kanazawa Ward, Yokohama 236-0004, Japan.

出版信息

Mol Neurobiol. 2012 Apr;45(2):234-46. doi: 10.1007/s12035-012-8242-4. Epub 2012 Feb 18.

DOI:10.1007/s12035-012-8242-4
PMID:22351471
Abstract

Collapsin response mediator protein (CRMP) was originally identified as a molecule involved in semaphorin3A signaling. CRMPs are now known to consist of five homologous cytosolic proteins, CRMP1-5. All of them are phosphorylated and highly expressed in the developing and adult nervous system. In vitro experiments have clearly demonstrated that CRMPs play important roles in neuronal development and maturation through the regulation of their phosphorylation. Several recent knockout mice studies have revealed in vivo roles of CRMPs in neuronal migration, neuronal network formation, synapse formation, synaptic plasticity, and neuronal diseases. Dynamic spatiotemporal regulation of phosphorylation status of CRMPs is involved in many aspects of neuronal development.

摘要

collapsin 反应介质蛋白 (CRMP) 最初被鉴定为参与信号 semaphorin3A 的分子。现在已知 CRMP 由五个同源胞质蛋白 CRMP1-5 组成。它们在发育和成年神经系统中均高度表达并发生磷酸化。体外实验清楚地表明,CRMP 通过调节其磷酸化在神经元发育和成熟中发挥重要作用。最近的一些敲除小鼠研究揭示了 CRMP 在神经元迁移、神经元网络形成、突触形成、突触可塑性和神经元疾病中的体内作用。CRMP 磷酸化状态的动态时空调节参与了神经元发育的许多方面。

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Phosphorylation of CRMP2 (collapsin response mediator protein 2) is involved in proper dendritic field organization.CRMP2( collapsin response mediator protein 2)的磷酸化参与了树突场的正确组织。
J Neurosci. 2012 Jan 25;32(4):1360-5. doi: 10.1523/JNEUROSCI.5563-11.2012.
2
CRMP4 suppresses apical dendrite bifurcation of CA1 pyramidal neurons in the mouse hippocampus.CRMP4 抑制小鼠海马 CA1 锥体神经元的树突分岔。
Dev Neurobiol. 2012 Nov;72(11):1447-57. doi: 10.1002/dneu.22007. Epub 2012 Jul 20.
3
Suppression of inflammatory and neuropathic pain by uncoupling CRMP-2 from the presynaptic Ca²⁺ channel complex.
解析关联:衔接蛋白 2 磷酸化在神经退行性变和神经再生中的作用
Neuromolecular Med. 2024 Nov 12;26(1):45. doi: 10.1007/s12017-024-08814-0.
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Hindbrain boundaries as niches of neural progenitor and stem cells regulated by the extracellular matrix proteoglycan chondroitin sulphate.后脑边界作为神经祖细胞和干细胞的龛位,由细胞外基质蛋白聚糖硫酸软骨素调控。
Development. 2024 Feb 15;151(4). doi: 10.1242/dev.201934. Epub 2024 Feb 13.
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Calpain signaling: from biology to therapeutic opportunities in neurodegenerative disorders.钙蛋白酶信号传导:从生物学原理到神经退行性疾病的治疗契机
Front Vet Sci. 2023 Sep 5;10:1235163. doi: 10.3389/fvets.2023.1235163. eCollection 2023.
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Contribution of the dihydropyrimidinase-like proteins family in synaptic physiology and in neurodevelopmental disorders.二氢嘧啶酶样蛋白家族在突触生理学和神经发育障碍中的作用。
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Protein Misfolding and Aggregation in the Brain: Common Pathogenetic Pathways in Neurodegenerative and Mental Disorders.脑内蛋白质错误折叠和聚集:神经退行性和精神障碍的常见发病机制途径。
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通过使 CRMP-2 与突触前 Ca²⁺ 通道复合物解偶联来抑制炎症和神经性疼痛。
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Emerging roles of collapsin response mediator proteins (CRMPs) as regulators of voltage-gated calcium channels and synaptic transmission.坍塌反应中介蛋白(CRMPs)作为电压门控钙通道和突触传递调节因子的新作用。
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10
Fyn promotes phosphorylation of collapsin response mediator protein 1 at tyrosine 504, a novel, isoform-specific regulatory site.Fyn 促进了神经反应调节蛋白 1 在酪氨酸 504 上的磷酸化,这是一个新的、异构体特异性的调节位点。
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