小胶质细胞
细胞生物学
线粒体分裂
线粒体
生物
氧化磷酸化
DNM1L型
促炎细胞因子
生物化学
炎症
免疫学
作者
Alejandro Montilla,Asier Ruiz,Mar Márquez,Amanda Sierra,Carlos Matute,Marı́a Domercq
出处
期刊:ImmunoHorizons
[The American Association of Immunologists]
日期:2021-08-01
卷期号:5 (8): 615-626
被引量:25
标识
DOI:10.4049/immunohorizons.2100068
摘要
-ATP synthase contributes to mitochondrial membrane potential. In addition, we studied the possible implication of mitochondrial dynamics in the metabolic switch using the mitochondrial division inhibitor-1 (Mdivi-1), which blocks dynamin-related protein 1 (Drp1)-dependent mitochondrial fission. Mdivi-1 significantly reduced the expression of proinflammatory markers in LPS plus IFN-γ-treated microglia. However, this inhibition did not lead to a recovery of the oxidative phosphorylation ablation by LPS plus IFN-γ or to a microglia repolarization. Altogether, these results suggest that Drp1-dependent mitochondrial fission, although potentially involved in microglial activation, does not play an essential role in metabolic reprogramming and repolarization of microglia.
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