Department of Pathophysiology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Int J Mol Sci. 2021 Dec 23;23(1):135. doi: 10.3390/ijms23010135.
Cerebral ischemia-reperfusion injury is related to inflammation driven by free mitochondrial DNA. At the same time, the pro-inflammatory activation of macrophages, that is, polarization in the M1 direction, aggravates the cycle of inflammatory damage. They promote each other and eventually transform macrophages/microglia into neurotoxic macrophages by improving macrophage glycolysis, transforming arginine metabolism, and controlling fatty acid synthesis. Therefore, we propose targeting the mtDNA-driven inflammatory response while controlling the metabolic state of macrophages in brain tissue to reduce the possibility of cerebral ischemia-reperfusion injury.
脑缺血再灌注损伤与由游离线粒体 DNA 驱动的炎症有关。同时,巨噬细胞的促炎激活,即 M1 方向的极化,加剧了炎症损伤的循环。它们相互促进,最终通过提高巨噬细胞糖酵解、改变精氨酸代谢和控制脂肪酸合成,将巨噬细胞/小胶质细胞转化为神经毒性巨噬细胞。因此,我们提出靶向 mtDNA 驱动的炎症反应,同时控制脑组织中巨噬细胞的代谢状态,以降低脑缺血再灌注损伤的可能性。