...
首页> 外文期刊>Brain research. Developmental brain research >Distribution of GAP-43 mRNA in the immature and adult cerebellum: a role for GAP-43 in cerebellar development and neuroplasticity.
【24h】

Distribution of GAP-43 mRNA in the immature and adult cerebellum: a role for GAP-43 in cerebellar development and neuroplasticity.

机译:GAP-43 mRNA在未成熟和成年小脑中的分布:GAP-43在小脑发育和神经可塑性中的作用。

获取原文
获取原文并翻译 | 示例
           

摘要

Expression of GAP-43 mRNA in the rat cerebellum and inferior olivary nucleus was examined at birth, during postnatal development and in the adult by both Northern and in situ hybridization. Northern blot analysis revealed that cerebellar GAP-43 mRNA expression increases from birth to postnatal day (PD) 7 and then declines to a lower level in the adult. At birth, in situ hybridization experiments showed intense labeling of GAP-43 mRNA in the premigratory, but not the germinal, zone of the cerebellar external granule cell layer. Localization of GAP-43 within the premigratory zone, a layer containing post-mitotic granule cells, indicates that granule cells begin expressing GAP-43 mRNA after final mitosis and during axonal outgrowth of the parallel fibers. The deep cerebellar nuclei and the inferior olive were also intensely labeled at birth. GAP-43 mRNA was localized in granule cells during their migration through the molecular layer of the developing cerebellum and after their arrival in the internal granule cell layer. By PD 21, the pattern of GAP-43 expression was similar to that observed in the adu GAP-43 mRNA was localized to the internal granule layer and the inferior olive with minimal to no hybridization in the deep cerebellar nuclei and none in the molecular layer. Purkinje cells were devoid of GAP-43 mRNA throughout the postnatal and adult periods. In light of our observations, we propose that GAP-43 is a critical factor in granule cell differentiation/migration, as well as in the parallel and climbing fiber axonal outgrowth and synaptogenesis during development. Localization of GAP-43 mRNA within granule and inferior olivary cells of adult animals indicates that GAP-43 protein observed in the molecular layer is transported from these cells to their terminals in the molecular layer suggesting that GAP-43 is also an intrinsic presynaptic determinant in cerebellar neuroplasticity.
机译:通过Northern和原位杂交检查出生时,产后发育期间和成年大鼠中小脑和下橄榄核中GAP-43 mRNA的表达。 Northern印迹分析显示,小脑GAP-43 mRNA表达从出生到出生后一天(PD)7都会增加,然后在成年人中降低到较低的水平。出生时,原位杂交实验显示小脑外部颗粒细胞层的迁移前区域(而非生发区域)强烈标记了GAP-43 mRNA。 GAP-43在迁移前区域(包含有丝分裂后的颗粒细胞)中的定位表明,颗粒细胞在最终有丝分裂后和平行纤维的轴突生长过程中开始表达GAP-43 mRNA。小脑深核和下橄榄在出生时也被强烈标记。 GAP-43 mRNA在通过发展中的小脑分子层的迁移过程中以及到达内部颗粒细胞层后都位于颗粒细胞中。通过PD 21,GAP-43的表达模式与成年人相似。 GAP-43 mRNA定位于内部颗粒层和下橄榄,在小脑深核中几乎没有杂交,在分子层中没有杂交。整个产后和成年期,浦肯野细胞都没有GAP-43 mRNA。根据我们的观察,我们认为GAP-43是颗粒细胞分化/迁移以及发育过程中平行和攀升纤维轴突生长和突触形成的关键因素。 GAP-43 mRNA在成年动物的颗粒和下橄榄细胞中的定位表明,在分子层中观察到的GAP-43蛋白从这些细胞转运到分子层的末端,这表明GAP-43还是内在的突触前决定簇。小脑神经可塑性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号