Goshima Yoshio
Department of Molecular Pharmacology and Neurobiology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Nihon Shinkei Seishin Yakurigaku Zasshi. 2006 Jun;26(3):135-40.
The functioning of the vertebrate brain depends on the differentiation and positioning of the neural cells, and on the specific connections these cells make among themselves and their peripheral targets. Semaphorin3A (Sema3A), a secreted type of guidance cue of the semaphorin family, possesses a strong repulsive activity to a subset of neurons such as dorsal root ganglia and sympathetic neurons. CRMP (collapsin response mediator protein) was originally identified as an intracellular mediator of Sema3A by using Xenopus laevis oocyte expression system, but its mechanism has long been ill-defined. We demonstrate that Fyn-Cdk5 complex acts as a downstream mediator of Sema3A signaling cascades that induce growth cone collapse. In addition, the sequential phosphorylation of CRMP2 by Cdk5 and GSK3beta is an important process of Sema3A signaling. Since the dual-phosphorylated CRMP2 is recognized with the antibody 3F4, a highly reactive antibody with the neurofibrillary tangles of Alzheimer's disease, the same mechanism for Sema3A signaling may have some relevance to the pathological aggregation of the microtubule-associated proteins.
脊椎动物大脑的功能取决于神经细胞的分化和定位,以及这些细胞之间及其与外周靶标之间形成的特定连接。信号素3A(Sema3A)是信号素家族分泌型的导向因子,对背根神经节和交感神经元等一部分神经元具有强烈的排斥活性。CRMP(塌陷反应介导蛋白)最初是通过非洲爪蟾卵母细胞表达系统被鉴定为Sema3A的细胞内介质,但其机制长期以来一直不清楚。我们证明Fyn-Cdk5复合物作为Sema3A信号级联反应的下游介质,诱导生长锥塌陷。此外,Cdk5和GSK3β对CRMP2的顺序磷酸化是Sema3A信号传导的重要过程。由于双磷酸化的CRMP2可被抗体3F4识别,3F4是一种与阿尔茨海默病神经原纤维缠结高度反应的抗体,Sema3A信号传导的相同机制可能与微管相关蛋白的病理聚集有一定关联。