Suppr超能文献

连接蛋白 36 的表达调控神经祖细胞向神经元的分化。

Connexin 36 expression regulates neuronal differentiation from neural progenitor cells.

机构信息

Henry Wellcome Laboratories for Integrative Neuroscience & Endocrinology, University of Bristol, Bristol, United Kingdom.

出版信息

PLoS One. 2011 Mar 9;6(3):e14746. doi: 10.1371/journal.pone.0014746.

Abstract

BACKGROUND

Gap junction communication has been shown in glial and neuronal cells and it is thought they mediate inter- and intra-cellular communication. Connexin 36 (Cx36) is expressed extensively in the developing brain, with levels peaking at P14 after which its levels fall and its expression becomes entirely neuronal. These and other data have led to the hypothesis that Cx36 may direct neuronal coupling and neurogenesis during development.

METHODOLOGY/PRINCIPAL FINDINGS: To investigate Cx36 function we used a neurosphere model of neuronal cell development and developed lentiviral Cx36 knockdown and overexpression strategies. Cx36 knockdown was confirmed by western blotting, immunocytochemistry and functionally by fluorescence recovery after photobleaching (FRAP). We found that knockdown of Cx36 in neurosphere neuronal precursors significantly reduced neuronal coupling and the number of differentiated neurons. Correspondingly, the lentiviral mediated overexpression of Cx36 significantly increased the number of neurons derived from the transduced neurospheres. The number of oligodendrocytes was also significantly increased following transduction with Cx36 indicating they may support neuronal differentiation.

CONCLUSIONS/SIGNIFICANCE: Our data suggests that astrocytic and neuronal differentiation during development are governed by mechanisms that include the differential expression of Cx36.

摘要

背景

缝隙连接通讯已在神经胶质细胞和神经元细胞中得到证实,据认为它们介导细胞内和细胞间的通讯。连接蛋白 36(Cx36)在发育中的大脑中广泛表达,其水平在 P14 达到峰值,之后其水平下降,表达完全变为神经元。这些和其他数据导致了这样的假设,即 Cx36 可能在发育过程中指导神经元偶联和神经发生。

方法/主要发现:为了研究 Cx36 的功能,我们使用了神经元细胞发育的神经球模型,并开发了慢病毒 Cx36 敲低和过表达策略。通过 Western blot、免疫细胞化学和荧光恢复后光漂白(FRAP)功能证实了 Cx36 的敲低。我们发现,神经球神经元前体细胞中 Cx36 的敲低显著降低了神经元偶联和分化神经元的数量。相应地,慢病毒介导的 Cx36 过表达显著增加了转导神经球衍生的神经元数量。转导后,少突胶质细胞的数量也显著增加,表明它们可能支持神经元分化。

结论/意义:我们的数据表明,发育过程中的星形胶质细胞和神经元分化受包括 Cx36 差异表达在内的机制控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c464/3052311/b369c2f5eb1c/pone.0014746.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验