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E 盒 Sox 基因 Sox8 和 Sox9 受 Notch 信号调控,对于小鼠视网膜 Müller 胶质细胞的发育是必需的。

The group E Sox genes Sox8 and Sox9 are regulated by Notch signaling and are required for Müller glial cell development in mouse retina.

机构信息

Department of Molecular and Developmental Biology, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokane-dai, Minato-ku, Tokyo 108-8639, Japan.

出版信息

Exp Eye Res. 2009 Oct;89(4):549-58. doi: 10.1016/j.exer.2009.05.006. Epub 2009 May 31.

Abstract

Although Müller glial cells play pivotal roles in the vertebrate retina, the regulation of their development is poorly understood. While Notch-Hes5 signaling has been shown to be involved in this developmental process, the presence of Müller glial cells in Hes5-deficient mice suggests the involvement of other molecules. We found that two group E Sox genes, Sox8 and Sox9, are expressed in proliferating progenitors and then exclusively in Müller glial cells in mouse retina. Knocking-down Sox8 and Sox9 by shRNA significantly reduced the population of Müller glial cells and relatively increased the proportion of rod photoreceptors, suggesting that the Sox genes play roles in the specification of Müller glial cells. Using an activated form of Notch and the gamma-secretase inhibitor DAPT, we also found that Notch signaling regulates the transcription of Sox8 and Sox9. This is the first evidence that group E Sox genes play important roles in the developing vertebrate retina.

摘要

虽然 Müller 胶质细胞在脊椎动物视网膜中起着关键作用,但它们的发育调控机制仍知之甚少。虽然 Notch-Hes5 信号通路已被证明参与了这一发育过程,但在 Hes5 缺陷型小鼠中存在 Müller 胶质细胞表明存在其他分子的参与。我们发现,两个 Sox 基因家族 E 成员 Sox8 和 Sox9,在增殖的祖细胞中表达,然后在小鼠视网膜的 Müller 胶质细胞中特异性表达。通过 shRNA 敲低 Sox8 和 Sox9,Müller 胶质细胞的数量显著减少,而杆状光感受器的比例相对增加,表明 Sox 基因在 Müller 胶质细胞的特化中起作用。使用 Notch 的激活形式和 γ-分泌酶抑制剂 DAPT,我们还发现 Notch 信号通路调节 Sox8 和 Sox9 的转录。这是 Sox 基因家族 E 成员在发育中的脊椎动物视网膜中发挥重要作用的第一个证据。

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