IGBMC Institut de Génétique et de Biologie Moléculaire et Cellulaire, Department of Development and Stem Cells, CNRS UMR7104, Inserm U964, Université de Strasbourg, Illkirch, France.
Cell Adh Migr. 2013 May-Jun;7(3):325-32. doi: 10.4161/cam.25140. Epub 2013 May 24.
Mutations in genes encoding several basal lamina components as well as their cellular receptors disrupt normal deposition and remodeling of the cortical basement membrane resulting in a disorganized cerebral and cerebellar cortex. The α6 integrin was the first α subunit associated with cortical lamination defects and formation of neural ectopias. In order to understand the precise role of α6 integrin in the central nervous system (CNS), we have generated mutant mice carrying specific deletion of α6 integrin in neuronal and glia precursors by crossing α6 conditional knockout mice with Nestin-Cre line. Cerebral cortex development occurred properly in the resulting α6 (fl/fl;nestin-Cre) mutant animals. Interestingly, however, cerebellum displayed foliation pattern defects although granule cell (GC) proliferation and migration were not affected. Intriguingly, analysis of Bergmann glial (BG) scaffold revealed abnormalities in fibers morphology associated with reduced processes outgrowth and altered actin cytoskeleton. Overall, these data show that α6 integrin receptors are required in BG cells to provide a proper fissure formation during cerebellum morphogenesis.
基因突变导致编码基底膜成分及其细胞受体的基因发生突变,从而破坏了皮质基底膜的正常沉积和重塑,导致大脑和小脑皮质排列紊乱。α6 整合素是第一个与皮质分层缺陷和神经外胚层形成相关的α 亚基。为了了解α6 整合素在中枢神经系统 (CNS) 中的精确作用,我们通过将α6 条件性敲除小鼠与巢蛋白-Cre 系杂交,在神经元和神经胶质前体细胞中产生了特异性缺失α6 整合素的突变小鼠。在产生的α6 (fl/fl;nestin-Cre) 突变动物中,大脑皮层的发育正常进行。然而,有趣的是,小脑显示出裂层模式缺陷,尽管颗粒细胞 (GC) 的增殖和迁移没有受到影响。有趣的是,对伯格曼胶质 (BG) 支架的分析显示,与突起生长减少和肌动蛋白细胞骨架改变相关的纤维形态异常。总的来说,这些数据表明,α6 整合素受体在 BG 细胞中是必需的,以在小脑形态发生过程中提供适当的裂隙形成。