内分泌学
内科学
脂肪性肝炎
雌激素受体
雌激素
基因敲除
胰岛素抵抗
非酒精性脂肪性肝炎
脂肪肝
CCR2型
下调和上调
非酒精性脂肪肝
医学
化学
受体
糖尿病
疾病
趋化因子
趋化因子受体
乳腺癌
生物化学
癌症
细胞凋亡
基因
作者
Zhiping Shu,Guopeng Zhang,Xiaohua Zhu,Wenqian Xiong
标识
DOI:10.1016/j.bbrc.2022.01.085
摘要
Owing to lacking protective effect of estrogen, OVX mice have higher risk of non-alcoholic fatty liver disease compared with normal female mice, when fed with high fat diet. Our study was to explore how estrogen protect against nonalcoholic steatohepatitis in female mice. We found that, lacking estrogen, M1 macrphages was activated and promoted steatohepatitis in obese OVX mice. And, ERα was responsible for estrogen to inhibit M1 macrphages activation and steatohepatitis. ERα knockdown aggravated M1 macrophages infiltration by transcriptionally upregulated its CCR2 expression. CCR2 antagonist effectively improved nonalcoholic steatohepatitis, ER stress and insulin resistance in ERα knockdown obese female mice. These results demonstrated ERα mediated M1 macrophages activation played a key role in nonalcoholic steatohepatitis.
科研通智能强力驱动
Strongly Powered by AbleSci AI