Collapsin Response Mediator Proteins Regulate Neuronal Development and Plasticity by Switching Their Phosphorylation Status

被引:95
作者
Yamashita, Naoya [1 ]
Goshima, Yoshio [1 ]
机构
[1] Yokohama City Univ, Grad Sch Med, Dept Mol Pharmacol & Neurobiol, Kanazawa Ward, Yokohama, Kanagawa 2360004, Japan
关键词
Collapsin response mediator protein; Semaphorin; Reelin; BDNF; Phosphorylation; GROWTH-CONE COLLAPSE; CYCLIN-DEPENDENT KINASE-5; AXON OUTGROWTH INHIBITION; CEREBELLAR PURKINJE-CELLS; APOE RECEPTOR 2; ALZHEIMERS-DISEASE; HIPPOCAMPAL-NEURONS; RHO-KINASE; NEURODEGENERATIVE DISEASES; MOLECULAR CHARACTERIZATION;
D O I
10.1007/s12035-012-8242-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:234 / 246
页数:13
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