Alharshawi Khaled, Fey Holger, Vogle Alyx, Klenk Tori, Kim Miran, Aloman Costica
Division of Digestive Diseases and Nutrition, Section of Hepatology, Rush University, Chicago, IL 60612, United States.
Division of Digestive Diseases and Nutrition, Section of Hepatology, Rush University, Chicago, IL 60612, United States.
Int Immunopharmacol. 2021 Jan;90:107166. doi: 10.1016/j.intimp.2020.107166. Epub 2020 Nov 14.
Alcoholic liver disease includes a spectrum of clinical and histological entities. They result from the combined direct effect of alcohol and its metabolites on immune cells and resident tissue cells. In humans and mice, females are more susceptible to alcoholic liver injury than males. Despite being involved in sex specific differences of immune mediated tissue injury, plasmacytoid dendritic cells (pDCs) have not been thoroughly assessed as a cellular target of alcohol in humans or mice. Therefore, Meadows-Cook diet was used to study alcohol effect on hepatic dendritic cells. Alcohol consumption for 12 weeks increased hepatic pDCs in female mice. The expression of the C-C chemokine receptor type 2 (CCR2) increased in hepatic pDC of alcohol-fed female mice. Bone marrow transplant chimera showed CCR2 dependent bone marrow egress of pDCs. Chronic alcohol exposure has a sex specific effect on hepatic pDCs population that may explain sex differences to alcoholic liver disease.
酒精性肝病包括一系列临床和组织学实体。它们是酒精及其代谢产物对免疫细胞和驻留组织细胞的联合直接作用所致。在人类和小鼠中,雌性比雄性更容易受到酒精性肝损伤。尽管浆细胞样树突状细胞(pDCs)参与了免疫介导的组织损伤的性别特异性差异,但在人类或小鼠中,pDCs作为酒精的细胞靶点尚未得到充分评估。因此,采用梅多斯 - 库克饮食来研究酒精对肝树突状细胞的影响。雌性小鼠连续12周饮酒会增加肝脏中的pDCs。在喂食酒精的雌性小鼠的肝脏pDC中,C - C趋化因子受体2(CCR2)的表达增加。骨髓移植嵌合体显示pDCs的CCR2依赖性骨髓迁出。慢性酒精暴露对肝脏pDCs群体有性别特异性影响,这可能解释了酒精性肝病的性别差异。