MIC-1 is a novel TGF-β superfamily cytokine associated with macrophage activation

被引:236
作者
Fairlie, WD
Moore, AG
Bauskin, AR
Russell, PK
Zhang, HP
Breit, SN
机构
[1] St Vincents Hosp, Ctr Immunol, Sydney, NSW 2010, Australia
[2] Univ New S Wales, Sydney, NSW, Australia
关键词
cDNA cloning; Northern blotting; autocrine inhibitors;
D O I
10.1002/jlb.65.1.2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
As part of a study to identify novel genes associated with macrophage activation, we hare cloned a new member of the transforming growth factor beta (TGF-beta) superfamily designated macrophage inhibitory cytokine 1 (MIC-1). MIC-1 is synthesized as a 62-kDa intracellular protein, which, after cleavage by a furin like protease, is secreted as a 25-kDa disulfide-linked dimeric protein. Sequence analysis indicates that it does not cluster within any existing TGF-beta families, suggesting it may he the first member of a new grouping within the TGF-beta superfamily. Tissue Northern blots show that MIC-1 transcripts are only found abundantly in placenta, although smaller amounts are seen in a limited number of other adult and fetal tissues. MIC-1 is not expressed in resting macrophages but is induced by a number of different activation agents, including phorbol myristate acetate, interleukin I, tumor necrosis factor or, and macrophage colony-stimulating factor but not by lipopolysaccharide or interferon-gamma, We have hypothesized that it may be an autocrine inhibitor of macrophage activation but its major biological role is still uncertain.
引用
收藏
页码:2 / 5
页数:4
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