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CREM-1 的上调与光诱导损伤后体内视网膜神经节细胞凋亡有关。

Upregulation of CREM-1 relates to retinal ganglion cells apoptosis after light-induced damage in vivo.

机构信息

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong Province, People's Republic of China.

出版信息

J Mol Neurosci. 2014 Mar;52(3):331-8. doi: 10.1007/s12031-013-0153-y. Epub 2013 Oct 30.

Abstract

Previous studies have shown activation of cyclic AMP response element-binding protein (CREB) family is involved in the retinal ganglion cells (RGCs) protection. However, the function of cyclic AMP response element modulator-1 (CREM-1), one member of the CREB family, is still with limited acquaintance. To investigate whether CREM-1 is involved in RGCs death, we performed a light-induced retinal damage model in adult rats. Upregulation of CREM-1 was observed in retina after light-induced damage by performing western blot. Immunofluorescent labeling indicated that upregulated CREM-1 was localized mainly in the RGCs. We also investigated co-localization of CREM-1 with active-caspase-3 and TUNEL (apoptotic markers) in the retina after light-induced damage. In addition, the expression patterns of B cell lymphoma/leukemia-2 and Bcl-2 associated X protein were parallel with that of CREM-1. Collectively, we hypothesized upregulation of CREM-1 in the retina was associated with RGCs death after light-induced damage.

摘要

先前的研究表明,环磷酸腺苷反应元件结合蛋白(CREB)家族的激活参与了视网膜神经节细胞(RGCs)的保护。然而,CREB 家族的一员,环磷酸腺苷反应元件调制器-1(CREM-1)的功能仍知之甚少。为了研究 CREM-1 是否参与 RGCs 的死亡,我们在成年大鼠中建立了光诱导的视网膜损伤模型。通过 Western blot 检测到光诱导损伤后视网膜中 CREM-1 的上调。免疫荧光标记表明,上调的 CREM-1 主要定位于 RGCs。我们还研究了光诱导损伤后视网膜中 CREM-1 与活性半胱天冬酶-3 和 TUNEL(凋亡标志物)的共定位。此外,B 细胞淋巴瘤/白血病-2 和 Bcl-2 相关 X 蛋白的表达模式与 CREM-1 平行。综上所述,我们假设光诱导损伤后视网膜中 CREM-1 的上调与 RGCs 的死亡有关。

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