脂肪性肝炎
肝细胞
细胞凋亡
癌症研究
化学
脂肪肝
内科学
医学
生物化学
体外
疾病
作者
Zhigang Lei,Jiaojiao Yu,Yu Wu,Junyao Shen,Shibo Lin,Weijie Xue,Chenxu Mao,Rui Tang,Haoran Sun,Xin Qi,Xiaohong Wang,Lei Xu,Chuan Wei,Xiaowei Wang,Hongbing Chen,Ping Hao,Wen Yin,Jifeng Zhu,Yalin Li,Yi Wu
标识
DOI:10.1016/j.jhep.2023.10.025
摘要
Excessive and/or sustained hepatocyte apoptosis is critical in driving liver inflammation and injury. The mechanisms underlying the regulation of hepatocyte apoptosis in non-alcoholic steatohepatitis (NASH) remain largely unclear. Here, we found that CD1d expression in hepatocytes substantially decreases and negatively correlates with the severity of liver injury in patients with NASH. We further revealed a previously unrecognized anti-apoptotic CD1d-JAK2-STAT3 signaling axis in hepatocytes, which confers significant protection against liver injury in NASH and acute liver diseases. Thus, hepatocyte CD1d-targeted therapy could be a promising strategy to manipulate liver injury in both NASH and other hepatocyte apoptosis-related liver diseases.
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