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NSCL-1和NSCL-2通过协调神经元前体细胞的迁移来控制小脑前核的形成。

NSCL-1 and -2 control the formation of precerebellar nuclei by orchestrating the migration of neuronal precursor cells.

作者信息

Schmid Thomas, Krüger Marcus, Braun Thomas

机构信息

Max-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany.

出版信息

J Neurochem. 2007 Sep;102(6):2061-2072. doi: 10.1111/j.1471-4159.2007.04694.x. Epub 2007 Jun 15.

Abstract

During embryonic development post-mitotic neurons of the precerebellar neuroepithelium, migrate from the rhombic lip to the ventral part of the neural tube to form the precerebellar nuclei of the pons and medulla oblongata. In this study, we show that neural basic helix-loop-helix transcription factors NSCL-1 and -2 are expressed in all cells of the anterior extramural migration stream (aes), which forms the precerebellar nuclei. The combined inactivation of NSCL-1 and -2 led to a complete absence of the pontine nuclei and a strong reduction in the reticulotegmental nuclei. We demonstrate that NSCL-1/2 were required for a sustained expression of the netrin receptor and cell guidance molecule Dcc in the aes. Unc5H3, a second netrin receptor, which serves as a stop signal for migratory cells was up-regulated in NSCL-1/2 deficient cells, which ceased migration and accumulated ectopically. Furthermore, we observed a massive increase of apoptosis in cells of the aes in the absence of NSCL-1/2, which together with the arrest of migration might explain the virtually complete loss of aes-derived structures in NSCL-1/2 mutant mice. We conclude that NSCL-1/2 maintain migration and survival of cells in the aes.

摘要

在胚胎发育过程中,小脑前神经上皮的有丝分裂后神经元从菱唇迁移至神经管腹侧,形成脑桥和延髓的小脑前核。在本研究中,我们发现神经碱性螺旋-环-螺旋转录因子NSCL-1和-2在前外侧壁迁移流(aes)的所有细胞中均有表达,而aes会形成小脑前核。NSCL-1和-2的联合失活导致脑桥核完全缺失,网状被盖核显著减少。我们证明,NSCL-1/2是aes中持续表达网蛋白受体和细胞导向分子Dcc所必需的。Unc5H3是另一种网蛋白受体,作为迁移细胞的停止信号,在NSCL-1/2缺陷细胞中上调,这些细胞停止迁移并异位聚集。此外,我们观察到在缺乏NSCL-1/2的情况下,aes细胞中的凋亡大量增加,这与迁移停滞一起,可能解释了NSCL-1/2突变小鼠中aes衍生结构几乎完全丧失的原因。我们得出结论,NSCL-1/2维持aes中细胞的迁移和存活。

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