单位:[1]Department of Hepatopancreatobiliary and Splenic Medicine , Affiliated Hospital, Logistics University of People's Armed Police Force , Tianjin , People's Republic of China.[2]Liver Research Center, Beijing Friendship Hospital, Capital Medial University , Beijing , People's Republic of China.临床科室国家中心肝病分中心首都医科大学附属北京友谊医院[3]State Key Laboratory of Proteomics, Beijing Proteome Research Center, Beijing Institute of Radiation Medicine , Beijing , People's Republic of China.
Hepatic macrophages account for the largest non-parenchymal cell population in the liver. Recent studies have found that hepatic macrophages have different functions in different stages of experimental liver fibrosis. Some studies found that there are different types of hepatic macrophages in the liver, although others have suggested that hepatic macrophages could switch to different phenotypes in different environments. Many studies demonstrated that while hepatic macrophages promoted fibrosis through the recruitment of proinflammatory immune cells, and the secretion of proinflammatory cytokines and chemokines in the early stages, these also promoted the resolution of hepatic fibrosis through the secretion of matrix metalloproteinases in the late stages. This article will review the current role played by hepatic macrophages in liver fibrosis and the potential therapeutic targets that modulate hepatic macrophages.
第一作者单位:[1]Department of Hepatopancreatobiliary and Splenic Medicine , Affiliated Hospital, Logistics University of People's Armed Police Force , Tianjin , People's Republic of China.
推荐引用方式(GB/T 7714):
Li Hai,You Hong,Fan Xu,et al.Hepatic macrophages in liver fibrosis: pathogenesis and potential therapeutic targets.[J].BMJ Open Gastroenterology.2016,3(1):e000079.doi:10.1136/bmjgast-2016-000079.
APA:
Li Hai,You Hong,Fan Xu&Jia Jidong.(2016).Hepatic macrophages in liver fibrosis: pathogenesis and potential therapeutic targets..BMJ Open Gastroenterology,3,(1)
MLA:
Li Hai,et al."Hepatic macrophages in liver fibrosis: pathogenesis and potential therapeutic targets.".BMJ Open Gastroenterology 3..1(2016):e000079