Horiguchi Norio, Wang Lei, Mukhopadhyay Partha, Park Ogyi, Jeong Won Il, Lafdil Fouad, Osei-Hyiaman Douglas, Moh Akira, Fu Xin Yuan, Pacher Pál, Kunos George, Gao Bin
Section on Liver Biology, Laboratory of Physiologic Studies, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland.
Gastroenterology. 2008 Apr;134(4):1148-58. doi: 10.1053/j.gastro.2008.01.016. Epub 2008 Jan 11.
BACKGROUND & AIMS: Signal transducer and activator of transcription 3 (STAT3) is known to be activated in human alcoholic liver disease, but its role in the pathogenesis of alcoholic liver injury remains obscure.
The role of STAT3 in alcoholic liver injury was investigated in hepatocyte-specific STAT3 knockout (H-STAT3KO) mice and macrophage/neutrophil-specific STAT3 KO (M/N-STAT3KO) mice. Alcoholic liver injury was achieved by feeding mice a liquid diet containing 5% ethanol for up to 8 weeks.
Compared with wild-type mice, feeding H-STAT3KO mice with an ethanol-containing diet induced greater hepatic steatosis, hypertriglyceridemia, and hepatic expression of lipogenic genes (sterol regulatory element-binding protein, fatty acid synthase, acetyl-CoA carboxylase-1, and stearoyl-CoA desaturase 1), but less inflammation and lower expression of hepatic proinflammatory cytokines. In contrast, ethanol-fed M/N-STAT3KO mice showed more hepatic inflammation, worse injury, and increased hepatic expression of proinflammatory cytokines compared with wild-type mice. Kupffer cells isolated from ethanol-fed H-STAT3KO mice produced similar amounts of reactive oxygen species and tumor necrosis factor alpha, whereas Kupffer cells from M/N-STAT3KO mice produced more reactive oxygen species and tumor necrosis factor alpha compared with wild-type controls.
These findings suggest that STAT3 regulates hepatic inflammation in a cell type-dependent manner during alcoholic liver injury: STAT3 in hepatocytes promotes whereas STAT3 in macrophages/Kupffer cells suppresses inflammation. In addition, activation of hepatocellular STAT3 ameliorates alcoholic fatty liver via inhibition of sterol regulatory element-binding protein 1c expression.
已知信号转导及转录激活因子3(STAT3)在人类酒精性肝病中被激活,但其在酒精性肝损伤发病机制中的作用仍不清楚。
在肝细胞特异性STAT3基因敲除(H-STAT3KO)小鼠和巨噬细胞/中性粒细胞特异性STAT3基因敲除(M/N-STAT3KO)小鼠中研究STAT3在酒精性肝损伤中的作用。通过给小鼠喂食含5%乙醇的液体饮食长达8周来诱导酒精性肝损伤。
与野生型小鼠相比,给H-STAT3KO小鼠喂食含乙醇饮食会诱导更严重的肝脏脂肪变性、高甘油三酯血症以及脂肪生成基因(固醇调节元件结合蛋白、脂肪酸合酶、乙酰辅酶A羧化酶-1和硬脂酰辅酶A去饱和酶1)的肝脏表达,但炎症较轻且肝脏促炎细胞因子的表达较低。相反,与野生型小鼠相比,喂食乙醇的M/N-STAT3KO小鼠表现出更多的肝脏炎症、更严重的损伤以及肝脏促炎细胞因子表达增加。从喂食乙醇的H-STAT3KO小鼠分离的库普弗细胞产生的活性氧和肿瘤坏死因子α量相似,而与野生型对照相比,M/N-STAT3KO小鼠的库普弗细胞产生更多的活性氧和肿瘤坏死因子α。
这些发现表明,在酒精性肝损伤期间,STAT3以细胞类型依赖的方式调节肝脏炎症:肝细胞中的STAT3促进炎症,而巨噬细胞/库普弗细胞中的STAT3抑制炎症。此外,肝细胞STAT3的激活通过抑制固醇调节元件结合蛋白1c的表达改善酒精性脂肪肝。