The activins and their binding protein, follistatin-Diagnostic and therapeutic targets in inflammatory disease and fibrosis

被引:114
作者
Hedger, M. P. [1 ]
de Kretser, D. M. [1 ]
机构
[1] Monash Univ, Monash Inst Med Res, Melbourne, Vic 3004, Australia
基金
英国医学研究理事会;
关键词
Activin; Follistatin; Inflammation; Fibrosis; Immunoregulation; GROWTH-FACTOR-BETA; ERYTHROID-DIFFERENTIATION FACTOR; INHIBIN-DEFICIENT MICE; TUMOR-NECROSIS-FACTOR; MARROW STROMAL CELLS; PANCREATIC STELLATE CELLS; OVARIAN GRANULOSA-CELL; MACROPHAGES IN-VITRO; REGULATORY T-CELLS; A GENE-EXPRESSION;
D O I
10.1016/j.cytogfr.2013.03.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The activins, as members of the transforming growth factor-beta superfamily, are pleiotrophic regulators of cell development and function, including cells of the myeloid and lymphoid lineages. Clinical and animal studies have shown that activin levels increase in both acute and chronic inflammation, and are frequently indicators of disease severity. Moreover, inhibition of activin action can reduce inflammation, damage, fibrosis and morbidity/mortality in various disease models. Consequently, activin A and, more recently, activin B are emerging as important diagnostic tools and therapeutic targets in inflammatory and fibrotic diseases. Activin antagonists such as follistatin, an endogenous activin-binding protein, offer considerable promise as therapies in conditions as diverse as sepsis, liver fibrosis, acute lung injury, asthma, wound healing and ischaemia-reperfusion injury. Crown Copyright (C) 2013 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:285 / 295
页数:11
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