败血症
下调和上调
成纤维细胞生长因子
组织因子
脂多糖
医学
凝结
蛋白激酶B
生长因子
PI3K/AKT/mTOR通路
免疫学
药理学
癌症研究
信号转导
内科学
生物
细胞生物学
受体
生物化学
基因
作者
Yuanyuan Sun,Fanrong Ye,Li Ding,Hongjing Yang,Tingting Xu,Xincun Zhong,Yilun Lu,Hongmin Zhou,Jingye Pan
标识
DOI:10.1016/j.taap.2023.116364
摘要
Sepsis is defined as a life-threatening organ dysfunction caused by dysregulation of the host response to infection. There is still a lack of specific treatment for sepsis. Here, we report that Fibroblast growth factor-2 (FGF2) can reduce the mortality of sepsis by ameliorating the coagulation abnormalities.FGF2 was intraperitoneally injected into septic mice induced by lipopolysaccharide (LPS) and then assessed for coagulation response, organ damage and survival. RAW264.7 cells with or without FGF2 pretreating were exposed to LPS, and then changes in coagulation related factors expression and signaling were tested.The findings showed that intraperitoneal injection of FGF2 inhibited coagulation activity, reduced lung and liver damage, and increased survival in septic mice. In RAW264.7 cells, LPS upregulated the expression of tissue factor (TF) and plasminogen activator inhibitor-1 (PAI-1); however, pretreatment with FGF2 prevented this upregulation, while FGF2 knockdown exacerbated TF upregulation. Moreover, FGF2 suppressing the AKT/mTOR/S6K1 signaling pathway in septic mice and RAW264.7 cells stimulated by LPS.This study revealed a therapeutic role of FGF2 in ameliorating the coagulation abnormalities during sepsis.
科研通智能强力驱动
Strongly Powered by AbleSci AI