Literature DB >> 14730603

Continuous enhanced expression of Hsc70 but not Hsp70 in rheumatoid arthritis synovial tissue.

Christoph Schick1, Martin Arbogast, Klaus Lowka, Rita Rzepka, Inga Melchers.   

Abstract

OBJECTIVE: To investigate the expression of constitutive and inducible members of the Hsp70 protein family in synovial tissue of patients with rheumatoid arthritis (RA) or osteoarthritis (OA).
METHODS: Frozen sections of synovial tissue and isolated synovial adherent cells obtained from 17 RA patients, 5 OA patients, and 1 patient with carpal tunnel syndrome (CTS) were analyzed with specific monoclonal antibodies, by immunohistochemistry, immunocytochemistry, and immunoblotting.
RESULTS: Expression of the constitutive chaperone Hsc70 was increased in synovial tissue from 9 of 9 patients with RA, but was faint or undetectable in 3 of 3 samples from patients with OA. In RA samples, cells mainly of the synovial lining stained intensely for Hsc70 as well as for HLA-DR, CD14, and CD68. Also, in vitro-cultured synovial adherent cells from 8 of 9 RA patients overexpressed Hsc70 (specimens from 1 RA patient were used in both the immunochemistry and the in vitro culture studies). On immunoblots of protein extracts, the synovial and HeLa cell molecules appeared identical in size. The inducible chaperone Hsp70 was not detected in samples from any of the same 17 RA patients, except for rare, isolated cells in 3. Samples from 4 of 5 OA patients also were negative for the inducible chaperone Hsp70, and the fifth was very weakly positive. In addition, tissue from 1 patient with CTS was analyzed 10 months before diagnosis of RA. Synovial tissue from this patient showed extreme overexpression of both Hsc70 and Hsp70.
CONCLUSION: In RA, synovial lining cells continuously overexpress Hsc70 but not Hsp70. Hsc70 may be up-regulated due to the high activity of these cells in several respects, including antigen processing and presentation.

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Year:  2004        PMID: 14730603     DOI: 10.1002/art.11426

Source DB:  PubMed          Journal:  Arthritis Rheum        ISSN: 0004-3591


  12 in total

1.  Commentary to: 'A comparison of two commercially available ELISA methods for the quantification of human plasma heat shock protein 70 during rest and exercise stress' by Lee et al. 2015.

Authors:  Janina Schwarzer; Gabriele Multhoff
Journal:  Cell Stress Chaperones       Date:  2015-08-04       Impact factor: 3.667

Review 2.  Interaction between HSP73 and HLA-DRB1*0401: implications for the development of rheumatoid arthritis.

Authors:  Isabelle Auger; Jean Roudier
Journal:  Immunol Res       Date:  2005       Impact factor: 2.829

Review 3.  [Immunogenetics--HLA-association, molecular chaperones and "related" diseases].

Authors:  I Melchers
Journal:  Z Rheumatol       Date:  2005-09       Impact factor: 1.372

Review 4.  Chaperones and proteases: cellular fold-controlling factors of proteins in neurodegenerative diseases and aging.

Authors:  Marie-Pierre Hinault; Anat Ben-Zvi; Pierre Goloubinoff
Journal:  J Mol Neurosci       Date:  2006       Impact factor: 3.444

5.  Analysis of serum heat shock protein 70 (HSPA1A) concentrations for diagnosis and disease activity monitoring in patients with rheumatoid arthritis.

Authors:  Seyed Reza Najafizadeh; Zaniar Ghazizadeh; Arash Aghajani Nargesi; Masoud Mahdavi; Shabnam Abtahi; Hossein Mirmiranpour; Manouchehr Nakhjavani
Journal:  Cell Stress Chaperones       Date:  2015-03-06       Impact factor: 3.667

6.  A comparison of two commercially available ELISA methods for the quantification of human plasma heat shock protein 70 during rest and exercise stress.

Authors:  B J Lee; N M Sukri; H Ogden; C Vine; C D Thake; J E Turner; J L J Bilzon
Journal:  Cell Stress Chaperones       Date:  2015-06-26       Impact factor: 3.667

7.  TXNDC5 synergizes with HSC70 to exacerbate the inflammatory phenotype of synovial fibroblasts in rheumatoid arthritis through NF-κB signaling.

Authors:  Lin Wang; Hongyan Dong; Guanhua Song; Rui Zhang; Jihong Pan; Jinxiang Han
Journal:  Cell Mol Immunol       Date:  2017-06-26       Impact factor: 11.530

Review 8.  The involvement of heat-shock proteins in the pathogenesis of autoimmune arthritis: a critical appraisal.

Authors:  Min-Nung Huang; Hua Yu; Kamal D Moudgil
Journal:  Semin Arthritis Rheum       Date:  2009-12-06       Impact factor: 5.532

9.  Heat shock protein 96 is elevated in rheumatoid arthritis and activates macrophages primarily via TLR2 signaling.

Authors:  Qi-Quan Huang; Rudina Sobkoviak; Angela R Jockheck-Clark; Bo Shi; Arthur M Mandelin; Paul Peter Tak; G Kennith Haines; Christopher V Nicchitta; Richard M Pope
Journal:  J Immunol       Date:  2009-04-15       Impact factor: 5.422

10.  Downregulation of heat shock protein 70 protects rheumatoid arthritis fibroblast-like synoviocytes from nitric oxide-induced apoptosis.

Authors:  Eun Ha Kang; Dong Jo Kim; Eun Young Lee; Yun Jong Lee; Eun Bong Lee; Yeong Wook Song
Journal:  Arthritis Res Ther       Date:  2009-08-27       Impact factor: 5.156

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