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TSG-6 interacts with hyaluronan and aggrecan in a pH-dependent manner via a common functional element: implications for its regulation in inflamed cartilage.

作者信息

Parkar A A, Kahmann J D, Howat S L, Bayliss M T, Day A J

机构信息

Department of Biochemistry, University of Oxford, UK.

出版信息

FEBS Lett. 1998 May 29;428(3):171-6. doi: 10.1016/s0014-5793(98)00523-7.

DOI:10.1016/s0014-5793(98)00523-7
PMID:9654129
Abstract

Cartilage matrix is stabilised by the interactions of proteins with hyaluronan (HA). We compare the pH dependences of HA binding by aggrecan, link protein and TSG-6. Aggrecan and link protein exhibit maximal binding across a wide pH range (6.0-8.0). TSG-6, a protein that is only produced during inflammation, binds maximally at about pH 6.0 but shows a dramatic loss of function with increasing pH. TSG-6 also interacts with aggrecan, with a similar pH dependence, and this can be inhibited by HA. Thus, a common binding surface on TSG-6 may be involved in HA and aggrecan binding. We propose that TSG-6 is involved in matrix dissociation and that this is regulated by pH gradients in cartilage.

摘要

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