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PMID: 16377621 Published · ppublish English Journal Article

The role of human HtrA1 in arthritic disease.

The Journal of biological chemistry ·Vol. 281 ·No. 10 ·2006-03-10 ·Pages 6124-9

Grau S, Richards PJ, Kerr B, Hughes C, Caterson B, Williams AS, Junker U, Jones SA, Clausen T, Ehrmann M

Abstract

Human HtrA1 belongs to a widely conserved family of serine proteases involved in various aspects of protein quality control and cell fate. Although HtrA1 has been implicated in the pathology of several diseases, its precise biological functions remain to be established. Through identification of potential HtrA1 targets, studies presented herein propose that within the context of arthritis pathology HtrA1 contributes to cartilage degradation. Elevated synovial HtrA1 levels were detected in fluids obtained from rheumatoid and osteoarthritis patients, with synovial fibroblasts identified as a major source of secreted HtrA1. Mass spectrometry analysis of potential HtrA1 substrates within synovial fluids identified fibronectin as a candidate target, and treatment of fibronectin with recombinant HtrA1 led to the generation of fibronectin-degradation products that may be involved in cartilage catabolism. Consistently, treatment of synovial fibroblasts with HtrA1 or HtrA1-generated fibronectin fragments resulted in the specific induction of matrix metalloprotease 1 and matrix metalloprotease 3 expression, suggesting that HtrA1 contributes to the destruction of extracellular matrix through both direct and indirect mechanisms.

MeSH Terms
Arthritis/enzymology,genetics,pathology Cartilage, Articular/enzymology,pathology Cells, Cultured Extracellular Matrix/enzymology,pathology Fibroblasts/enzymology Fibronectins/metabolism High-Temperature Requirement A Serine Peptidase 1 Humans Matrix Metalloproteinases/biosynthesis,genetics Peptide Fragments/metabolism RNA, Messenger/metabolism Recombinant Proteins/chemistry,genetics,isolation & purification Serine Endopeptidases/genetics,isolation & purification,physiology Substrate Specificity Synovial Fluid/enzymology Tissue Inhibitor of Metalloproteinases/biosynthesis,genetics
Chemicals
Fibronectins Peptide Fragments RNA, Messenger Recombinant Proteins Tissue Inhibitor of Metalloproteinases High-Temperature Requirement A Serine Peptidase 1 HtrA1 protein, human Serine Endopeptidases Matrix Metalloproteinases
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Grau Sandra
School of Biosciences, Cardiff University, Cardiff CF10 3US, United Kingdom.
Richards Peter J
Kerr Briedgeen
Hughes Clare
Caterson Bruce
Williams Anwen S
Junker Uwe
Jones Simon A
Clausen Tim
Ehrmann Michael
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2006-03-10
Epub
2005-00-22
Pages
6124-9
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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