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The Influence of Mitochondrial-DNA-Driven Inflammation Pathways on Macrophage Polarization: A New Perspective for Targeted Immunometabolic Therapy in Cerebral Ischemia-Reperfusion Injury

Journal

Publisher

MDPI
DOI: 10.3390/ijms23010135

Keywords

cerebral ischemia-reperfusion; mtDNA; inflammation; macrophages; immune metabolism; STING

Funding

  1. National Natural Science Foundation of China [82102733, 81772794]
  2. Jilin Provincial Research Foundation for the Development of Science and Technology Projects [20200703009ZP, 20190201164JC, 20191008011TC]
  3. Jilin Provincial Health Technology Innovation Project [2021JC034, 2018SCZ021]

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Cerebral ischemia-reperfusion injury is associated with inflammation caused by free mitochondrial DNA, and the pro-inflammatory activation of macrophages exacerbates the damage. By controlling the metabolic state of macrophages and targeting the mtDNA-driven inflammatory response, the possibility of injury can be reduced.
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.

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