Li Le, Stary Creed M
Department of Anesthesiology, Perioperative & Pain Medicine, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305-5117, USA; Department of Anesthesiology, Zhujiang Hospital, Southern Medical University, 253 Industrial Road, Guangzhou, Guangdong Province 510280, China.
Department of Anesthesiology, Perioperative & Pain Medicine, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305-5117, USA.
Oxid Med Cell Longev. 2016;2016:6032306. doi: 10.1155/2016/6032306. Epub 2016 Sep 29.
Astrocytes and microglia play crucial roles in the response to cerebral ischemia and are effective targets for stroke therapy in animal models. MicroRNAs (miRs) are important posttranscriptional regulators of gene expression that function by inhibiting the translation of select target genes. In astrocytes, miR expression patterns regulate mitochondrial function in response to oxidative stress targeting of Bcl2 and heat shock protein 70 family members. Mitochondria play an active role in microglial activation, and miRs regulate the microglial neuroinflammatory response. As endogenous miR expression patterns can be altered with exogenous mimics and inhibitors, miR-targeted therapies represent a viable intervention to optimize glial mitochondrial function and improve clinical outcome following cerebral ischemia. In the present article, we review the role that astrocytes and microglia play in neuronal function and fate following ischemic stress, discuss the relevance of mitochondria in the glial response to injury, and present current evidence implicating miRs as critical regulators in the glial mitochondrial response to cerebral ischemia.
星形胶质细胞和小胶质细胞在脑缺血反应中发挥着关键作用,并且在动物模型中是中风治疗的有效靶点。微小RNA(miR)是基因表达的重要转录后调节因子,其通过抑制特定靶基因的翻译发挥作用。在星形胶质细胞中,miR表达模式通过靶向Bcl2和热休克蛋白70家族成员来调节线粒体功能以应对氧化应激。线粒体在小胶质细胞激活中发挥积极作用,而miR调节小胶质细胞的神经炎症反应。由于内源性miR表达模式可通过外源性模拟物和抑制剂改变,因此基于miR的疗法是一种可行的干预措施,可优化胶质细胞线粒体功能并改善脑缺血后的临床结局。在本文中,我们综述了星形胶质细胞和小胶质细胞在缺血应激后神经元功能和命运中所起的作用,讨论了线粒体在胶质细胞对损伤反应中的相关性,并提供了当前证据表明miR是胶质细胞线粒体对脑缺血反应的关键调节因子。