ATF3
肝细胞核因子
肝细胞核因子4
转录因子
激活转录因子
癌症研究
炎症
脂肪肝
核受体
生物
内分泌学
肝细胞
脂肪性肝炎
下调和上调
化学
肝细胞生长因子
细胞生物学
基因敲除
内科学
肝损伤
法尼甾体X受体
孕烷X受体
医学
生物化学
发起人
基因表达
基因
体外
疾病
作者
Yanyong Xu,Shuwei Hu,Kavita Jadhav,Yingdong Zhu,Xiaoli Pan,Fathima Cassim Bawa,Liya Yin,Yanqiao Zhang
出处
期刊:Diabetes
[American Diabetes Association]
日期:2021-09-02
卷期号:70 (11): 2506-2517
被引量:6
摘要
Activating transcription factor 3 (ATF3) has been shown to play an important role in HDL metabolism; yet, the role of hepatocytic ATF3 in the development of steatohepatitis remains elusive. Here we show that adenoassociated virus-mediated overexpression of human ATF3 in hepatocytes prevents diet-induced steatohepatitis in C57BL/6 mice and reverses steatohepatitis in db/db mice. Conversely, global or hepatocyte-specific loss of ATF3 aggravates diet-induced steatohepatitis. Mechanistically, hepatocytic ATF3 induces hepatic lipolysis and fatty acid oxidation and inhibits inflammation and apoptosis. We further show that hepatocyte nuclear factor 4α (HNF4α) is required for ATF3 to improve steatohepatitis. Thus, the current study indicates that ATF3 protects against steatohepatitis through, at least in part, hepatic HNF4α. Targeting hepatic ATF3 may be useful for treatment of steatohepatitis.
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