生物
炎症
败血症
清道夫受体
受体
细胞生物学
免疫学
药理学
内分泌学
生物化学
胆固醇
脂蛋白
作者
Gang Liang,Jia‐Yan Hu,Rou‐Jun Liu,Yu‐Peng Chao,Y. Hu,Hong Zheng,Xinyu Pan,Yuan‐Jing Li,Yang‐Hui Gong,Chi Lin,Jiahao Lin,J. H. Wang,Tong‐Xin Li,Jianping Pan,Duan Guo
标识
DOI:10.1002/eji.202350655
摘要
Abstract Sepsis arises from an uncontrolled inflammatory response triggered by infection or stress, accompanied by alteration in cellular energy metabolism, and a strong correlation exists between these factors. Alpha‐ketoglutarate (α‐KG), an intermediate product of the TCA cycle, has the potential to modulate the inflammatory response and is considered a crucial link between energy metabolism and inflammation. The scavenger receptor (SR‐A5), a significant pattern recognition receptor, assumes a vital function in anti‐inflammatory reactions. In the current investigation, we have successfully illustrated the ability of α‐KG to mitigate inflammatory factors in the serum of septic mice and ameliorate tissue damage. Additionally, α‐KG has been shown to modulate metabolic reprogramming and macrophage polarization. Moreover, our findings indicate that the regulatory influence of α‐KG on sepsis is mediated through SR‐A5. We also elucidated the mechanism by which α‐KG regulates SR‐A5 expression and found that α‐KG reduced the N6‐methyladenosine level of macrophages by up‐regulating the m 6 A demethylase ALKBH5. α‐KG plays a crucial role in inhibiting inflammation by regulating SR‐A5 expression through m6A demethylation during sepsis. The outcomes of this research provide valuable insights into the relationship between energy metabolism and inflammation regulation, as well as the underlying molecular regulatory mechanism.
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