Inhibition of matrix metalloproteinase-9 by interferons and TGF-β1 through distinct signalings accounts for reduced monocyte invasiveness

被引：27

作者：

Nguyen, J ^{[1
]}

Knapnougel, P ^{[1
]}

Lesavre, P ^{[1
]}

Bauvois, B ^{[1
]}

机构：

[1] Hop Necker Enfants Malad, INSERM 507, F-75015 Paris, France

来源：

FEBS LETTERS | 2005年 / 579卷 / 25期

关键词：

IRF-1; transmigration; MMP-9; STAT1; PTK; signaling;

D O I：

10.1016/j.febslet.2005.09.012

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：

Cytokines may provide signals for regulating human monocyte matrix metalloproteinase-9 (MMP-9) activity. In this study, we investigated the roles of interferons (IFN) type I/II and transforming growth factor-beta 1 (TGF-beta 1) in MMP-9-mediated invasiveness. MMP-9 antibody and inhibitor, IFNs and TGF-beta 1 inhibited monocyte transmigration through Matrigel. IFNs and TGF-beta 1 downregulated MMP-9 mRNA, protein and activity levels. The inhibitory action of IFNs was associated with the STAT1/IRF-1 pathway since the JAK inhibitor AG490 blocked STAT1 phosphorylation, IRF-1 synthesis and counteracted the blockade of MMP-9 release. TGF-P1-mediated MMP-9 inhibition appeared STAT1/IRF-1-independent but reversed by the protein tyrosine kinase inhibitor tyrphostin 25. Our data point out the importance of IFNs and TGF-beta 1 in the control of monocyte MMP-9-mediated extravasation. (c) 2005 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.

引用

页码：5487 / 5493

页数：7

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