Yu Wei-Ming, Chen Zu-Lin, North Alison J, Strickland Sidney
Laboratory of Neurobiology and Genetics, The Rockefeller University, New York, NY 10065, USA.
J Cell Sci. 2009 Apr 1;122(Pt 7):929-36. doi: 10.1242/jcs.033928.
Development of the peripheral nervous system requires radial axonal sorting by Schwann cells (SCs). To accomplish sorting, SCs must both proliferate and undergo morphogenetic changes such as process extension. Signaling studies reveal pathways that control either proliferation or morphogenesis, and laminin is essential for SC proliferation. However, it is not clear whether laminin is also required for SC morphogenesis. By using a novel time-lapse live-cell-imaging technique, we demonstrated that laminins are required for SCs to form a bipolar shape as well as for process extension. These morphological deficits are accompanied by alterations in signaling pathways. Phosphorylation of Schwannomin at serine 518 and activation of Rho GTPase Cdc42 and Rac1 were all significantly decreased in SCs lacking laminins. Inhibiting Rac1 and/or Cdc42 activities in cultured SCs attenuated laminin-induced myelination, whereas forced activation of Rac1 and/or Cdc42 in vivo improved sorting and hypomyelinating phenotypes in SCs lacking laminins. These findings indicate that laminins play a pivotal role in regulating SC cytoskeletal signaling. Coupled with previous results demonstrating that laminin is critical for SC proliferation, this work identifies laminin signaling as a central regulator coordinating the processes of proliferation and morphogenesis in radial axonal sorting.
外周神经系统的发育需要施万细胞(SCs)进行径向轴突分选。为了完成分选,施万细胞必须增殖并经历形态发生变化,如突起延伸。信号研究揭示了控制增殖或形态发生的途径,层粘连蛋白对施万细胞增殖至关重要。然而,尚不清楚层粘连蛋白对施万细胞形态发生是否也是必需的。通过使用一种新型的延时活细胞成像技术,我们证明层粘连蛋白对于施万细胞形成双极形状以及突起延伸是必需的。这些形态学缺陷伴随着信号通路的改变。在缺乏层粘连蛋白的施万细胞中,神经纤维瘤蛋白在丝氨酸518处的磷酸化以及Rho GTP酶Cdc42和Rac1的激活均显著降低。在培养的施万细胞中抑制Rac1和/或Cdc42活性会减弱层粘连蛋白诱导的髓鞘形成,而在体内强制激活Rac1和/或Cdc42可改善缺乏层粘连蛋白的施万细胞中的分选和髓鞘形成不足表型。这些发现表明层粘连蛋白在调节施万细胞细胞骨架信号中起关键作用。结合先前表明层粘连蛋白对施万细胞增殖至关重要的结果,这项工作确定层粘连蛋白信号是协调径向轴突分选中增殖和形态发生过程的核心调节因子。