Source:http://linkedlifedata.com/resource/pubmed/id/17261541
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2007-4-19
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pubmed:abstractText |
To elucidate the specific function of m-calpain in the metabolism of aggrecan in human articular cartilage, the prevalence and localization of a large glycosaminoglycan-bearing aggrecan product generated by m-calpain in human osteoarthritis (OA) cartilage were investigated. Extracts of human OA articular cartilage were analysed by immunostaining using new polyclonal anti-VPGVA antiserum that detects the COOH terminal neoepitope IVTQVVPGVA(709) generated by m-calpain-related cleavage within the keratan sulphate rich region of human aggrecan. Immunoblotting analyses of aggrecan populations in guanidine hydrochloride-extracts showed that OA cartilages contained anti-VPGVA positive aggrecan products with the COOH terminal neoepitope ... VPGVA(709), resulting from truncation between the Ala(709)-Ala(710) m-calpain-related cleavage site. This aggrecan product consisted of two NH(2) terminal globular domain (G1 and G2) and KS side chains. Immunohistochemical staining showed that anti-VPGVA positive staining was localized within chondrocytes and spread to the surrounding interterritorial matrix. Confocal microscopic analysis showed subcellular colocalization of anti-VPGVA and anti m-calpain. These results indicate that the aggrecan product with the COOH terminal neoepitope VPGVA(709) is synthesized regularly by intracellular processing in chondrocytes, and is present abundantly as a limited form of aggrecan. M-calpain is the major candidate of the proteinase to generate this aggrecan product during the intracellular aggrecan processing.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Aggrecans,
http://linkedlifedata.com/resource/pubmed/chemical/Calpain,
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes,
http://linkedlifedata.com/resource/pubmed/chemical/Keratan Sulfate,
http://linkedlifedata.com/resource/pubmed/chemical/m-calpain
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0021-924X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
141
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
469-77
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pubmed:dateRevised |
2007-12-19
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pubmed:meshHeading |
pubmed-meshheading:17261541-Aggrecans,
pubmed-meshheading:17261541-Animals,
pubmed-meshheading:17261541-Blotting, Western,
pubmed-meshheading:17261541-Calpain,
pubmed-meshheading:17261541-Cartilage, Articular,
pubmed-meshheading:17261541-Chondrocytes,
pubmed-meshheading:17261541-Epitopes,
pubmed-meshheading:17261541-Humans,
pubmed-meshheading:17261541-Keratan Sulfate,
pubmed-meshheading:17261541-Osteoarthritis,
pubmed-meshheading:17261541-Swine
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pubmed:year |
2007
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pubmed:articleTitle |
G1-G2 aggrecan product that can be generated by M-calpain on truncation at Ala709-Ala710 is present abundantly in human articular cartilage.
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pubmed:affiliation |
Department of Orthopaedic Surgery, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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