The G1 domain of aggrecan released from porcine articular cartilage forms stable complexes with hyaluronan/link protein
Objective. To raise peptide antibodies recognizing the C‐terminal amino acid sequence in the G1 domain of porcine aggrecan, generated by the action of either aggrecanase or neutral metalloproteinase(s), in rabbits and to use them to investigate the release of aggrecan from porcine articular cartilag...
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Published in | Rheumatology (Oxford, England) Vol. 42; no. 2; pp. 336 - 342 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Oxford University Press
01.02.2003
Oxford Publishing Limited (England) |
Subjects | |
Online Access | Get full text |
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Summary: | Objective. To raise peptide antibodies recognizing the C‐terminal amino acid sequence in the G1 domain of porcine aggrecan, generated by the action of either aggrecanase or neutral metalloproteinase(s), in rabbits and to use them to investigate the release of aggrecan from porcine articular cartilage. Method. An explant culture system was used to investigate the release of the G1 domain of aggrecan from porcine articular cartilage treated with retinoic acid or interleukin 1β and to study how the activity of these agents is modified by the proteinase inhibitor, batimastat (BB94). Results. Retinoic acid and interleukin 1β induced both enzyme activities and the release of the G1 domain into the culture medium. Proteinase activity was significantly reduced when the tissue was incubated in the presence of BB94. The functional properties of the enzyme‐generated G1 domain were studied using large‐pore, agarose/polyacrylamide gel electrophoresis, and it was shown to interact with hyaluronan and link protein. Conclusions. The results show that there must be a mechanism for removing a functional G1 domain from aggrecan during tissue turnover using this culture system. |
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Bibliography: | local:420336 istex:66296E0494F36BEC0C799BE5C78D2D1DE2D1C94C PII:1460-2172 ark:/67375/HXZ-D7ZZJ7F8-4 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1462-0324 1462-0332 |
DOI: | 10.1093/rheumatology/keg109 |