Wallace Michael C, Friedman Scott L, Mann Derek A
Division of Liver Diseases, Mount Sinai School of Medicine, New York, New York.
Fibrosis Laboratory, Institute of Cellular Medicine, New Castle University, Newcastle upon Tyne, United Kingdom.
Semin Liver Dis. 2015 May;35(2):107-18. doi: 10.1055/s-0035-1550060. Epub 2015 May 14.
The last decade has seen a rapid expansion in our understanding of the mechanisms leading to hepatic stellate cell activation. The classic activation pathway of initiation, perpetuation and regression remains as a useful model; however, the emergence of several new pathways and mediators has revealed a deeper complexity than previously appreciated. Although core fibrogenic pathways exist across organs and disease types, there is accumulating evidence for disease- and context-specific mechanisms that may modulate or drive hepatic fibrogenesis. Hence, a "one size fits all" approach to antifibrotic therapy may not be appropriate for all disease settings. The authors present a focused and concise update of the most recent advances in our understanding of hepatic stellate cell activation pathways, while highlighting several challenges that may be constraining progress. This summary provides a foundation to further expand our knowledge of this unique cell type and its contributions to human liver disease.
在过去十年中,我们对导致肝星状细胞激活机制的理解有了迅速扩展。启动、持续和消退的经典激活途径仍然是一个有用的模型;然而,几种新途径和介质的出现揭示了比以前认识到的更深层次的复杂性。尽管核心纤维化途径存在于各种器官和疾病类型中,但越来越多的证据表明,特定疾病和背景的机制可能调节或驱动肝纤维化。因此,抗纤维化治疗的“一刀切”方法可能并不适用于所有疾病情况。作者聚焦并简要介绍了我们对肝星状细胞激活途径理解的最新进展,同时强调了可能限制进展的几个挑战。本综述为进一步扩展我们对这种独特细胞类型及其对人类肝脏疾病贡献的认识奠定了基础。