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缺氧预处理的神经保护作用:缺氧诱导因子-1和促红细胞生成素可保护视网膜免于退化。

Neuroprotection by hypoxic preconditioning: HIF-1 and erythropoietin protect from retinal degeneration.

作者信息

Grimm C, Hermann D M, Bogdanova A, Hotop S, Kilic U, Wenzel A, Kilic E, Gassmann M

机构信息

Laboratory of Retinal Cell Biology, University Eye Hospital Zurich, CH-8091 Zurich, Switzerland.

出版信息

Semin Cell Dev Biol. 2005 Aug-Oct;16(4-5):531-8. doi: 10.1016/j.semcdb.2005.03.004. Epub 2005 Apr 18.

Abstract

Hypoxic exposure of cells or organisms induces expression of a number of hypoxia responsive genes through the activation of the hypoxia-inducible factor-1 (HIF-1). One of the most prominent HIF-1 targets is erythropoietin that has beneficial effects on ischemia-related injury in the brain. Exposure to low environmental oxygen concentrations can be used as a preconditioning paradigm to protect cells or tissues against a variety of harmful conditions. Here, we summarize recent work on neuroprotection of retinal photoreceptors and ganglion cells induced by hypoxic preconditioning or by systemically elevated levels of Epo in mouse plasma.

摘要

细胞或生物体的低氧暴露通过缺氧诱导因子-1(HIF-1)的激活诱导许多缺氧反应基因的表达。HIF-1最显著的靶标之一是促红细胞生成素,它对脑缺血相关损伤具有有益作用。暴露于低环境氧浓度可作为一种预处理模式,以保护细胞或组织免受各种有害条件的影响。在此,我们总结了近期关于低氧预处理或小鼠血浆中Epo全身水平升高对视网膜光感受器和神经节细胞神经保护作用的研究工作。

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