Jiménez-Mateos Eva M, Wandosell Francisco, Reiner Orly, Avila Jesús, González-Billault Christian
Centro de Biología Molecular Severo Ochoa, CSIC-UAM, Campus de Cantoblanco, Cantoblanco 28049, Madrid, Spain.
Biochem J. 2005 Jul 15;389(Pt 2):333-41. doi: 10.1042/BJ20050244.
For neuronal migration to occur, the cell must undergo morphological changes that require modifications of the cytoskeleton. Several different MAPs (microtubule-associated proteins) or actin-binding proteins are proposed to be involved in the migration of neurons. Therefore we have specifically analysed how two members of the MAP family, MAP1B and LIS1 (lissencephaly-related protein 1), interact with one another and participate in neuronal migration. Our results indicate that, in hippocampal neurons, MAP1B and LIS1 co-localize, associate and interact with each another. The interaction between these two MAPs is regulated by the phosphorylation of MAP1B. Furthermore, this interaction interferes with the association between LIS1 and the microtubule-dependent molecular motor, dynein. Clearly, the differential binding of these cytoskeletal proteins could regulate the functions attributed to the LIS1-dynein complex, including those related to extension of the neural processes necessary for neuronal migration.
为了使神经元迁移发生,细胞必须经历需要细胞骨架修饰的形态变化。几种不同的微管相关蛋白(MAPs)或肌动蛋白结合蛋白被认为参与了神经元的迁移。因此,我们专门分析了MAP家族的两个成员,即MAP1B和LIS1(无脑回相关蛋白1)如何相互作用并参与神经元迁移。我们的结果表明,在海马神经元中,MAP1B和LIS1共定位、缔合并相互作用。这两种MAP之间的相互作用受MAP1B磷酸化的调节。此外,这种相互作用干扰了LIS1与微管依赖性分子马达动力蛋白之间的缔合。显然,这些细胞骨架蛋白的差异结合可能调节归因于LIS1-动力蛋白复合体的功能,包括那些与神经元迁移所需神经突起延伸相关的功能。