Understanding the origin, activation and regulation of matrix-producing myofibroblasts for treatment of fibrotic disease

被引:228
作者
Kramann, Rafael [1 ,2 ,3 ]
DiRocco, Derek P. [1 ,2 ]
Humphreys, Benjamin D. [1 ,2 ,4 ]
机构
[1] Brigham & Womens Hosp, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Rhein Westfal TH Aachen, Div Nephrol, Aachen, Germany
[4] Harvard Stem Cell Inst, Cambridge, MA USA
基金
美国国家卫生研究院;
关键词
pericyte; myofibroblast; fibrosis; interstitium; GROWTH-FACTOR RECEPTOR; BLEOMYCIN-INDUCED PNEUMONOPATHY; AMELIORATES RENAL FIBROSIS; TO-MESENCHYMAL TRANSITION; MARROW-DERIVED CELLS; TGF-BETA; FACTOR-ALPHA; PULMONARY-FIBROSIS; INTERSTITIAL FIBROSIS; ALVEOLAR MACROPHAGES;
D O I
10.1002/path.4253
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Fibrosis and scar formation results from chronic progressive injury in virtually every tissue and affects a growing number of people around the world. Myofibroblasts drive fibrosis, and recent work has demonstrated that mesenchymal cells, including pericytes and perivascular fibroblasts, are their main progenitors. Understanding the cellular mechanisms of pericyte/fibroblast-to-myofibroblast transition, myofibroblast proliferation and the key signalling pathways that regulate these processes is essential to develop novel targeted therapeutics for the growing patient population suffering from solid organ fibrosis. In this review, we summarize the current knowledge about different progenitor cells of myofibroblasts, discuss major pathways that regulate their transdifferentiation and discuss the current status of novel targeted anti-fibrotic therapeutics in development. Copyright (c) 2013 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:273 / 289
页数:17
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