线粒体
粒体自噬
细胞生物学
炎症
小胶质细胞
胞浆
生物
细胞外
线粒体融合
细胞内
肿瘤坏死因子α
MFN2型
程序性细胞死亡
活性氧
氧化磷酸化
线粒体DNA
免疫学
细胞凋亡
自噬
生物化学
基因
酶
作者
Jack van Horssen,Pauline van Schaik,Maarten E. Witte
标识
DOI:10.1016/j.neulet.2017.06.050
摘要
Experimental evidence supports an intricate association between inflammation and mitochondrial dysfunction as main contributors of neurological diseases. Inflammatory mediators produced by activated microglia and infiltrated immune cells trigger intracellular signalling cascades that can alter cellular mitochondrial metabolism. Cytokines, particularly tumor necrosis factor-alpha, impede mitochondrial oxidative phosphorylation and associated ATP production and instigate mitochondrial reactive oxygen species production. This culminates in mitochondrial membrane permeabilization, altered mitochondrial dynamics and might ultimately result in cell death. When severely injured mitochondria are not appropriately removed by mitophagy they can release their contents into the cytosol and extracellular environment and thereby amplify the inflammatory process. Here we provide a comprehensive overview on how inflammatory mediators impair mitochondrial metabolism and discuss how defective mitochondria can elicit and potentiate an inflammatory response.
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