Liver Disease Research Center, Case Western Reserve University, Cleveland, Ohio, USA.
Compr Physiol. 2013 Apr;3(2):785-97. doi: 10.1002/cphy.c120026.
Kupffer cells are a critical component of the mononuclear phagocytic system and are central to both the hepatic and systemic response to pathogens. Kupffer cells are reemerging as critical mediators of both liver injury and repair. Kupffer cells exhibit a tremendous plasticity; depending on the local metabolic and immune environment, then can express a range of polarized phenotypes, from the proinflammatory M1 phenotype to the alternative/M2 phenotype. Multiple M2 phenotypes can be distinguished, each involved in the resolution of inflammation and wound healing. Here, we have provided an update on recent research that has contributed to the developing delineation of the contribution of Kupffer cells to different types of liver injury, with an emphasis on alcoholic and nonalcoholic liver diseases. These recent advances in our understanding of Kupffer cell function and regulation will likely provide new insights into the potential for therapeutic manipulation of Kupffer cells to promote the resolution of inflammation and enhance wound healing in liver disease.
枯否细胞是单核吞噬细胞系统的一个关键组成部分,是肝脏和全身对病原体反应的核心。枯否细胞正在重新成为肝脏损伤和修复的关键介质。枯否细胞表现出巨大的可塑性;根据局部代谢和免疫环境,它们可以表达一系列极化表型,从促炎的 M1 表型到替代性/M2 表型。可以区分出多种 M2 表型,每种表型都参与炎症的消退和伤口愈合。在这里,我们提供了最新的研究进展,这些研究有助于阐明枯否细胞对不同类型肝损伤的贡献,重点是酒精性和非酒精性肝病。这些关于枯否细胞功能和调节的最新认识,可能为治疗性干预枯否细胞以促进炎症消退和增强肝病中的伤口愈合提供新的见解。