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ADAMTS proteinases: a multi-domain, multi-functional family with roles in extracellular matrix turnover and arthritis
Members of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) family are known to influence development, angiogenesis, coagulation and progression of arthritis. As proteinases their substrates include the von Willebrand factor precursor and extracellular matrix components su...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1175049/ https://www.ncbi.nlm.nih.gov/pubmed/15987500 http://dx.doi.org/10.1186/ar1783 |
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author | Jones, Gavin C Riley, Graham P |
author_facet | Jones, Gavin C Riley, Graham P |
author_sort | Jones, Gavin C |
collection | PubMed |
description | Members of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) family are known to influence development, angiogenesis, coagulation and progression of arthritis. As proteinases their substrates include the von Willebrand factor precursor and extracellular matrix components such as procollagen, hyalectans (hyaluronan-binding proteoglycans including aggrecan), decorin, fibromodulin and cartilage oligomeric matrix protein. ADAMTS levels and activities are regulated at multiple levels through the control of gene expression, mRNA splicing, protein processing and inhibition by TIMP (tissue inhibitor of metalloproteinases). A recent screen of human cartilage has shown that multiple members of the ADAMTS family may be important in connective tissue homeostasis and pathology. |
format | Text |
id | pubmed-1175049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-11750492005-07-14 ADAMTS proteinases: a multi-domain, multi-functional family with roles in extracellular matrix turnover and arthritis Jones, Gavin C Riley, Graham P Arthritis Res Ther Review Members of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) family are known to influence development, angiogenesis, coagulation and progression of arthritis. As proteinases their substrates include the von Willebrand factor precursor and extracellular matrix components such as procollagen, hyalectans (hyaluronan-binding proteoglycans including aggrecan), decorin, fibromodulin and cartilage oligomeric matrix protein. ADAMTS levels and activities are regulated at multiple levels through the control of gene expression, mRNA splicing, protein processing and inhibition by TIMP (tissue inhibitor of metalloproteinases). A recent screen of human cartilage has shown that multiple members of the ADAMTS family may be important in connective tissue homeostasis and pathology. BioMed Central 2005 2005-06-21 /pmc/articles/PMC1175049/ /pubmed/15987500 http://dx.doi.org/10.1186/ar1783 Text en Copyright © 2005 BioMed Central Ltd |
spellingShingle | Review Jones, Gavin C Riley, Graham P ADAMTS proteinases: a multi-domain, multi-functional family with roles in extracellular matrix turnover and arthritis |
title | ADAMTS proteinases: a multi-domain, multi-functional family with roles in extracellular matrix turnover and arthritis |
title_full | ADAMTS proteinases: a multi-domain, multi-functional family with roles in extracellular matrix turnover and arthritis |
title_fullStr | ADAMTS proteinases: a multi-domain, multi-functional family with roles in extracellular matrix turnover and arthritis |
title_full_unstemmed | ADAMTS proteinases: a multi-domain, multi-functional family with roles in extracellular matrix turnover and arthritis |
title_short | ADAMTS proteinases: a multi-domain, multi-functional family with roles in extracellular matrix turnover and arthritis |
title_sort | adamts proteinases: a multi-domain, multi-functional family with roles in extracellular matrix turnover and arthritis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1175049/ https://www.ncbi.nlm.nih.gov/pubmed/15987500 http://dx.doi.org/10.1186/ar1783 |
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