The roles of activin A and its binding protein, follistatin, in inflammation and tissue repair

被引:152
作者
de Kretser, David M.
O'Hehir, Robyn E.
Hardy, Charles L.
Hedger, Mark P.
机构
[1] Monash Univ, Monash Inst Med Res, Clayton, Vic 3800, Australia
[2] Monash Univ, Dept Pathol & Immunol, Clayton, Vic 3800, Australia
[3] Alfred Hosp, Dept Allergy Immunol & Resp Med, Melbourne, Vic 3004, Australia
关键词
Activin; Follistatin; Inflammation; Fibrosis; Infection markers in blood; GROWTH-FACTOR-BETA; COLONY-STIMULATING FACTOR; MARROW STROMAL CELLS; MACROPHAGES IN-VITRO; T-CELLS; SIGNALING PATHWAYS; LANGERHANS CELLS; GENE-EXPRESSION; CYTOKINE; DIFFERENTIATION;
D O I
10.1016/j.mce.2011.10.009
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Activin A, a member of the transforming growth factor-beta superfamily of cytokines, is a critical controller of inflammation, immunity and fibrosis. It is rapidly released into the blood following a lipopolysaccharide challenge in experimental animals, through activation of the Toll-like receptor 4 signalling pathway. Blocking activin action by pre-treatment with its binding protein, follistatin, modifies the inflammatory cytokine cascade, and reduces the severity of the subsequent inflammatory response and mortality. Likewise, high serum levels of activin A are predictive of death in patients with septicaemia. However, activin A has complex immunomodulatory actions. It is produced by inflammatory macrophages, but can regulate either pro- or anti-inflammatory responses in these cells, depending on their prior activation status. Activin A is also produced by Th2 cells, and stimulates antibody production by B cells and the development of regulatory T cells. Production of activin A during inflammatory responses stimulates fibrosis and tissue remodelling, and follistatin inhibits these actions of activin A. The modulation of activin by follistatin may represent an important therapeutic target for the modulation and amelioration of inflammatory and fibrotic disorders. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:101 / 106
页数:6
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