Literature DB >> 7759957

Matrix metalloproteinases and processing of pro-TNF-alpha.

A J Gearing1, P Beckett, M Christodoulou, M Churchill, J M Clements, M Crimmin, A H Davidson, A H Drummond, W A Galloway, R Gilbert.   

Abstract

Tumor necrosis factor-alpha (TNF-alpha) is released from a cell membrane-anchored precursor by proteolytic cleavage. We have shown that broad spectrum synthetic inhibitors of matrix metalloproteinases (MMPs) prevent the processing of the TNF precursor but do not inhibit the release of other cytokines. Purified MMPs, stromelysin, matrilysin, collagenase, and the gelatinases can all cleave a recombinant pro-TNF substrate to yield mature TNF. MMP inhibitors prevent the rise in blood levels of TNF after endotoxin administration in rats and are effective in animal models of inflammatory disease such as adjuvant arthritis. Drugs that inhibit MMP action and TNF release show great promise for the treatment of autoimmune inflammatory diseases.

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Year:  1995        PMID: 7759957     DOI: 10.1002/jlb.57.5.774

Source DB:  PubMed          Journal:  J Leukoc Biol        ISSN: 0741-5400            Impact factor:   4.962


  63 in total

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8.  Epilysin (MMP-28) restrains early macrophage recruitment in Pseudomonas aeruginosa pneumonia.

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10.  Clinical predictors and management of hemorrhagic transformation.

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