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PMID: 9165065 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Activation mechanisms of matrix metalloproteinases.

Biological chemistry ·Vol. 378 ·No. 3-4 ·1997-00-00 ·Pages 151-60

Nagase H

Abstract

Matrix metalloproteinases (MMPs), also called matrixins, function in the turnover of extracellular matrix components. These enzymes are considered to play important roles in embryo development, morphogenesis and tissue remodeling, and in diseases such as arthritis, periodontitis, glomerulonephritis, atherosclerosis, tissue ulceration, and in cancer cell invasion and metastasis. All MMPs are synthesized as preproenzymes and most of them are secreted from the cells as proenzymes. Thus, the activation of these proenzymes is one of the critical steps that leads to extracellular matrix breakdown. This review describes recent progress made to elucidate the activation mechanisms of pro-matrixins which include extracellular stepwise activation common to most proMMPs, cell surface activation of progelatinase A and procollagenase 3, and intracellular activation of prostromelysin 3 and pro-membrane-type-1 MMP.

MeSH Terms
Amino Acid Sequence Animals Cysteine/chemistry Enzyme Activation Extracellular Matrix/enzymology Humans Metalloendopeptidases/metabolism Molecular Sequence Data
Chemicals
Metalloendopeptidases Cysteine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Nagase H
Department of Biochemistry and Molecular Biology, University of Kansas Medical Center, Kansas City 66160, USA.
Article Info
Journal
Biological chemistry
Abbr.
Biol Chem
ISSN
1431-6730
Published
1997-00-00
Pages
151-60
Language
English
Region
Germany
NLM ID
9700112
Subset
IM
Grants
NIAMS NIH HHS · AR39189 · United States
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