Bansal Meena B
Division of Liver Diseases, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, Box 1123, New York, NY, 10029, USA.
Hepatol Int. 2016 Nov;10(6):902-908. doi: 10.1007/s12072-016-9758-x. Epub 2016 Aug 30.
Since their original identification, our understanding of the role of hepatic stellate cells in both health and disease continues to grow. Numerous studies have delineated the role of stellate cell activation in contributing to the pool of myofibroblasts responsible for liver fibrosis, and these have resulted in the development of a number of anti-fibrotic strategies targeting this cell. However, their potential role in liver regeneration, both initiation and termination, is also emerging and needs to be contemplated when considering targeted therapy. Perhaps what is most striking is the increasing recognition that this is not just one cell, but rather, a heterogenous population made up of a number of different subsets of cells, each with differentiated and specific functions. The tools are emerging for this dissection and are greatly needed to truly develop targeted therapies that will inhibit fibrosis while promoting liver regeneration and repair.
自从最初被识别以来,我们对肝星状细胞在健康和疾病中的作用的理解一直在不断深入。大量研究已经阐明了星状细胞激活在导致负责肝纤维化的肌成纤维细胞池形成中的作用,这些研究催生了许多针对这种细胞的抗纤维化策略。然而,它们在肝再生的起始和终止过程中的潜在作用也逐渐显现,在考虑靶向治疗时需要加以思考。也许最引人注目的是,人们越来越认识到这不仅仅是一种细胞,而是由许多不同细胞亚群组成的异质性群体,每个亚群都有不同的分化和特定功能。用于剖析这一群体的工具正在出现,并且对于真正开发既能抑制纤维化又能促进肝再生和修复的靶向治疗来说是非常必要的。