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DNA 结合螺旋-环-螺旋蛋白抑制剂在发育中和成年小鼠视网膜中的表达和作用。

The expression and roles of inhibitor of DNA binding helix-loop-helix proteins in the developing and adult mouse retina.

机构信息

Department of Anatomy, The University of Hong Kong, Pokfulam, Hong Kong.

出版信息

Neuroscience. 2011 Feb 23;175:367-79. doi: 10.1016/j.neuroscience.2010.12.007. Epub 2010 Dec 9.

DOI:10.1016/j.neuroscience.2010.12.007
PMID:21145943
Abstract

Inhibitor of DNA binding (Id) proteins bind to and inhibit the function of basic helix-loop-helix (bHLH) transcription factors including those that regulate retinal development. However, little is known about the role of Id proteins in the growth and differentiation of the retina during development. The purpose of this study is to observe the expression of Id proteins in the developing and adult mouse retinas as the first step in investigating the functions of Id family members in the eye. The expression of Id1-4 was examined by real-time PCR, Western blot, and immunohistochemistry in wild-type and Id1/Id3 double-knockout mice. Id1-4 genes and proteins showed high expression levels in the retina at embryonic and early postnatal stages, whereas declined in the adult. Expression of Id proteins was observed in the inner neuroblastic layer (NBL) at embryonic (E) day 13.5 through 16.5. Id4 expression began at E18.5. By E18.5 and postnatal day 1, the expression of Id1-4 exhibited distinct yet overlapping patterns in the ganglion cell layer and inner part of NBL. In the adult, Ids were expressed in retinal ganglion cells, amacrine cells, bipolar cells, and horizontal cells. No Id expression was found in Müller cells. Id1 and Id3 double-knockout mice (Id1(-/-)/Id3(-/-)) showed smaller retinal size compared to wild-type or heterozygous littermates. However, histological analyses in Id1 and Id3 single-knockout retinas revealed no obvious defects in developmental phenotype. Our results indicate that the expression of the Id family may play an important role in regulating retinal progenitor cell proliferation and differentiation.

摘要

DNA 结合抑制因子(Id)蛋白与碱性螺旋-环-螺旋(bHLH)转录因子结合并抑制其功能,包括那些调节视网膜发育的转录因子。然而,关于 Id 蛋白在发育过程中视网膜生长和分化中的作用知之甚少。本研究的目的是观察 Id 蛋白在发育中和成年小鼠视网膜中的表达,作为研究 Id 家族成员在眼睛中的功能的第一步。通过实时 PCR、Western blot 和免疫组织化学,在野生型和 Id1/Id3 双敲除小鼠中检查 Id1-4 的表达。Id1-4 基因和蛋白在胚胎和出生后早期的视网膜中表达水平较高,而在成年时表达水平下降。在胚胎(E)第 13.5 天至 16.5 天,Id 蛋白在视网膜内层神经节细胞层(NBL)中表达。Id4 的表达始于 E18.5。到 E18.5 和出生后第 1 天,Id1-4 的表达在神经节细胞层和 NBL 内层具有明显但重叠的模式。在成年期,Id 表达于视网膜神经节细胞、无长突细胞、双极细胞和水平细胞中。在 Müller 细胞中未检测到 Id 表达。Id1 和 Id3 双敲除小鼠(Id1(-/-)/Id3(-/-))的视网膜大小明显小于野生型或杂合子同窝仔鼠。然而,在 Id1 和 Id3 单敲除视网膜的组织学分析中,未发现发育表型有明显缺陷。我们的结果表明,Id 家族的表达可能在调节视网膜祖细胞增殖和分化中发挥重要作用。

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