Bidirectional regulation of macrophage function by TGF-β

被引:168
作者
Ashcroft, GS [1 ]
机构
[1] Natl Inst Craniofacial & Dent Res, Oral Infect & Immun Branch, NIH, Bethesda, MD 20892 USA
关键词
TGF-beta; macrophage function; deactivation; reactivation; bidirectional regulation;
D O I
10.1016/S1286-4579(99)00257-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The dual role of transforming growth factor-beta (TGF-beta) in modulating macrophage function is an important concept gaining increasing recognition. In addition to its role as a 'macrophage-deactivating' agent, TGF-beta functions as a monocyte activator, inducing cytokine production and mediating host defence. These functions are context-dependent, modulated by the differentiation state of the cell, the local cytokine environment, and the local levels of TGF-beta in itself. In general, during the initial stages of inflammation, TGF-beta locally acts as a proinflammatory agent by recruiting and activating resting monocytes. As these cells differentiate specific immunosuppressive actions of TGF-beta predominate, leading to resolution of the inflammatory response. Increasing our understanding of the bidirectional regulation of macrophage function will facilitate prediction of the ultimate outcome of modulating TGF-beta levels in vivo. (C) 1999 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:1275 / 1282
页数:8
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