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Math3和NeuroD调节视网膜中无长突细胞的命运特化。

Math3 and NeuroD regulate amacrine cell fate specification in the retina.

作者信息

Inoue Tomoyuki, Hojo Masato, Bessho Yasumasa, Tano Yasuo, Lee Jacqueline E, Kageyama Ryoichiro

机构信息

Institute for Virus Research, Kyoto University, Kyoto 606-8507, Japan.

出版信息

Development. 2002 Feb;129(4):831-42. doi: 10.1242/dev.129.4.831.

Abstract

The basic helix-loop-helix genes Math3 and NeuroD are expressed by differentiating amacrine cells, retinal interneurons. Previous studies have demonstrated that a normal number of amacrine cells is generated in mice lacking either Math3 or NEUROD: We have found that, in Math3-NeuroD double-mutant retina, amacrine cells are completely missing, while ganglion and Müller glial cells are increased in number. In the double-mutant retina, the cells that would normally differentiate into amacrine cells did not die but adopted the ganglion and glial cell fates. Misexpression studies using the developing retinal explant cultures showed that, although Math3 and NeuroD alone only promoted rod genesis, they significantly increased the population of amacrine cells when the homeobox gene Pax6 or Six3 was co-expressed. These results indicate that Math3 and NeuroD are essential, but not sufficient, for amacrine cell genesis, and that co-expression of the basic helix-loop-helix and homeobox genes is required for specification of the correct neuronal subtype.

摘要

碱性螺旋-环-螺旋基因Math3和NeuroD在分化的无长突细胞(视网膜中间神经元)中表达。先前的研究表明,在缺乏Math3或NEUROD的小鼠中会产生正常数量的无长突细胞:我们发现,在Math3-NeuroD双突变视网膜中,无长突细胞完全缺失,而神经节细胞和米勒胶质细胞的数量增加。在双突变视网膜中,那些通常会分化为无长突细胞的细胞并未死亡,而是转变成了神经节细胞和胶质细胞的命运。利用发育中的视网膜外植体培养物进行的错误表达研究表明,尽管单独的Math3和NeuroD仅促进视杆细胞生成,但当同源框基因Pax6或Six3共表达时,它们会显著增加无长突细胞的数量。这些结果表明,Math3和NeuroD对于无长突细胞的发生是必不可少的,但并不充分,并且碱性螺旋-环-螺旋基因和同源框基因的共表达对于正确神经元亚型的特化是必需的。

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