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微小RNA在脑缺血情况下影响BCL-2家族蛋白。

MicroRNAs affect BCL-2 family proteins in the setting of cerebral ischemia.

作者信息

Ouyang Yi-Bing, Giffard Rona G

机构信息

Department of Anesthesia, Stanford University School of Medicine, Stanford, CA 94305, USA.

出版信息

Neurochem Int. 2014 Nov;77:2-8. doi: 10.1016/j.neuint.2013.12.006. Epub 2013 Dec 25.

Abstract

The BCL-2 family is centrally involved in the mechanism of cell death after cerebral ischemia. It is well known that the proteins of the BCL-2 family are key regulators of apoptosis through controlling mitochondrial outer membrane permeabilization. Recent findings suggest that many BCL-2 family members are also directly involved in controlling transmission of Ca(2+) from the endoplasmic reticulum (ER) to mitochondria through a specialization called the mitochondria-associated ER membrane (MAM). Increasing evidence supports the involvement of microRNAs (miRNAs), some of them targeting BCL-2 family proteins, in the regulation of cerebral ischemia. In this mini-review, after highlighting current knowledge about the multiple functions of BCL-2 family proteins and summarizing their relationship to outcome from cerebral ischemia, we focus on the regulation of BCL-2 family proteins by miRNAs, especially miR-29 which targets multiple BCL-2 family proteins.

摘要

BCL-2家族在脑缺血后的细胞死亡机制中起着核心作用。众所周知,BCL-2家族蛋白通过控制线粒体外膜通透性,是细胞凋亡的关键调节因子。最近的研究结果表明,许多BCL-2家族成员还通过一种名为线粒体相关内质网膜(MAM)的特殊结构,直接参与控制钙离子从内质网(ER)向线粒体的传递。越来越多的证据支持微小RNA(miRNA)参与脑缺血的调节,其中一些miRNA靶向BCL-2家族蛋白。在本综述中,在强调关于BCL-2家族蛋白多种功能的现有知识并总结它们与脑缺血预后的关系之后,我们重点关注miRNA对BCL-家族蛋白的调节,尤其是靶向多种BCL-2家族蛋白的miR-29。

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