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紫外线B诱导晶状体上皮细胞中Otx2的表达促进上皮-间充质转化。

Ultraviolet B-induced Otx2 expression in lens epithelial cells promotes epithelial-mesenchymal transition.

作者信息

Yoshitomi Yasuo, Osada Hiromi, Satake Haruka, Kojima Masami, Saito-Takatsuji Hidehito, Ikeda Takayuki, Yoshitake Yoshino, Ishigaki Yasuhito, Kubo Eri, Sasaki Hiroshi, Yonekura Hideto

机构信息

Department of Biochemistry, Kanazawa Medical University School of Medicine, 1-1 Daigaku, Uchinada, Kahoku-gun, Ishikawa 920-0293, Japan.

Department of Ophthalmology, Kanazawa Medical University School of Medicine, 1-1 Daigaku, Uchinada, Kahoku-gun, Ishikawa 920-0293, Japan.

出版信息

Biol Open. 2019 Feb 18;8(2):bio035691. doi: 10.1242/bio.035691.

Abstract

Ultraviolet (UV) radiation of eyes is a major risk factor for cataractogenesis, although the molecular mechanisms underlying this process remain poorly understood and genes that are affected by UV radiation have not been fully identified. In this study, we examined the UV-related gene regulation in lens epithelial cells (LECs) of mouse eyes and investigated the molecular mechanisms of UV-triggered cataractogenesis. Forty-one genes were significantly upregulated in LECs following UVB exposure in two independent experiments. Among these, Otx2 was strongly upregulated in LECs, suggesting that it may act as an upstream regulator of UVB-induced changes in gene expression. Accordingly, Otx2 overexpression in LECs induced morphological changes in cell shapes. Epithelial-mesenchymal transition (EMT)-related molecules, such as TGFβ2, αSMA and fibronectin were upregulated in Otx2-overexpressing LECs, concomitant with suppression of lens fiber cell marker genes, such as CRYAA and DNASEIIB. experiments suggested that UVB upregulated Otx2 through hydrogen peroxide generation. Aberrant upregulation of Otx2 in LECs following UV irradiation induces the EMT and alteration of the lens cell characteristics, likely contributing to cataractogenesis.

摘要

眼睛的紫外线(UV)辐射是白内障发生的主要危险因素,尽管这一过程背后的分子机制仍知之甚少,且受紫外线辐射影响的基因尚未完全确定。在本研究中,我们检测了小鼠眼睛晶状体上皮细胞(LECs)中与紫外线相关的基因调控,并研究了紫外线引发白内障发生的分子机制。在两项独立实验中,紫外线B(UVB)照射后,LECs中有41个基因显著上调。其中,Otx2在LECs中强烈上调,表明它可能作为UVB诱导基因表达变化的上游调节因子。因此,LECs中Otx2的过表达诱导了细胞形态的变化。上皮-间质转化(EMT)相关分子,如TGFβ2、αSMA和纤连蛋白在Otx2过表达的LECs中上调,同时晶状体纤维细胞标记基因,如CRYAA和DNASEIIB受到抑制。实验表明,UVB通过产生过氧化氢上调Otx2。紫外线照射后LECs中Otx2的异常上调诱导了EMT和晶状体细胞特性的改变,可能导致白内障的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d7e/6398467/52a4f952c6c6/biolopen-8-035691-g1.jpg

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