胶质发生
生物
视网膜
穆勒胶质细胞
细胞生物学
细胞命运测定
神经发育
视网膜
遗传学
螺旋
增强子
基因
神经科学
神经干细胞
基因表达
生物化学
祖细胞
干细胞
转录因子
DNA结合蛋白
作者
Tetsu Satow,Soo-Kyung Bae,Tomoyuki Inoue,Chihiro Inoue,Goichi Miyoshi,Koichi Tomita,Yasumasa Bessho,Nobuo Hashimoto,Ryoichiro Kageyama
标识
DOI:10.1523/jneurosci.21-04-01265.2001
摘要
Members of a subclass of hairy / Enhancer of split [ E(spl) ] homologs, called hesr genes, are structurally related to another subclass of hairy / E(spl) homologs, Hes genes, which play an important role in neural development. To characterize the roles of hesr genes in neural development, we used the retina as a model system. In situ hybridization analysis indicated that all hesr genes are expressed in the developing retina, but only hesr2 expression is associated spatially with gliogenesis. Each member was then misexpressed with retrovirus in the retinal explant cultures prepared from mouse embryos or neonates, which well mimic in vivo retinal development. Interestingly, hesr2 but not hesr1 or hesr3 promoted gliogenesis while inhibiting rod genesis without affecting cell proliferation or death, suggesting that the cells that normally differentiate into rods adopted the glial fate by misexpression of hesr2 . The gliogenic activity of hesr2 was more profound when it was misexpressed postnatally than prenatally. In addition, double mutation of the neuronal determination genes Mash1 and Math3 , which increases Müller glia at the expense of bipolar cells, upregulated hesr2 expression. These results indicate that, among structurally related hesr genes, only hesr2 promotes glial versus neuronal cell fate specification in the retina and that antagonistic regulation between hesr2 and Mash1–Math3 may determine the ratios of neurons and glia.
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