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Characterization and Localization of Citrullinated Proteoglycan Aggrecan in Human Articular Cartilage

BACKGROUND: Rheumatoid arthritis (RA) is an autoimmune disease of the synovial joints. The autoimmune character of RA is underscored by prominent production of autoantibodies such as those against IgG (rheumatoid factor), and a broad array of joint tissue-specific and other endogenous citrullinated...

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Autores principales: Glant, Tibor T., Ocsko, Timea, Markovics, Adrienn, Szekanecz, Zoltan, Katz, Robert S., Rauch, Tibor A., Mikecz, Katalin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778950/
https://www.ncbi.nlm.nih.gov/pubmed/26943656
http://dx.doi.org/10.1371/journal.pone.0150784
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author Glant, Tibor T.
Ocsko, Timea
Markovics, Adrienn
Szekanecz, Zoltan
Katz, Robert S.
Rauch, Tibor A.
Mikecz, Katalin
author_facet Glant, Tibor T.
Ocsko, Timea
Markovics, Adrienn
Szekanecz, Zoltan
Katz, Robert S.
Rauch, Tibor A.
Mikecz, Katalin
author_sort Glant, Tibor T.
collection PubMed
description BACKGROUND: Rheumatoid arthritis (RA) is an autoimmune disease of the synovial joints. The autoimmune character of RA is underscored by prominent production of autoantibodies such as those against IgG (rheumatoid factor), and a broad array of joint tissue-specific and other endogenous citrullinated proteins. Anti-citrullinated protein antibodies (ACPA) can be detected in the sera and synovial fluids of RA patients and ACPA seropositivity is one of the diagnostic criteria of RA. Studies have demonstrated that RA T cells respond to citrullinated peptides (epitopes) of proteoglycan (PG) aggrecan, which is one of the most abundant macromolecules of articular cartilage. However, it is not known if the PG molecule is citrullinated in vivo in human cartilage, and if so, whether citrulline-containing neoepitopes of PG (CitPG) can contribute to autoimmunity in RA. METHODS: CitPG was detected in human cartilage extracts using ACPA+ RA sera in dot blot and Western blot. Citrullination status of in vitro citrullinated recombinant G1 domain of human PG (rhG1) was confirmed by antibody-based and chemical methods, and potential sites of citrullination in rhG1 were explored by molecular modeling. CitPG-specific serum autoantibodies were quantified by enzyme-linked immunosorbent assays, and CitPG was localized in osteoarthritic (OA) and RA cartilage using immunohistochemistry. FINDINGS: Sera from ACPA+ RA patients reacted with PG purified from normal human cartilage specimens. PG fragments (mainly those containing the G1 domain) from OA or RA cartilage extracts were recognized by ACPA+ sera but not by serum from ACPA- individuals. ACPA+ sera also reacted with in vitro citrullinated rhG1 and G3 domain-containing fragment(s) of PG. Molecular modeling suggested multiple sites of potential citrullination within the G1 domain. The immunohistochemical localization of CitPG was different in OA and RA cartilage. CONCLUSIONS: CitPG is a new member of citrullinated proteins identified in human joints. CitPG could be found in both normal and diseased cartilage specimens. Antibodies against CitPG may trigger or augment arthritis by forming immune complexes with this autoantigen in the joints of ACPA+ RA patients.
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spelling pubmed-47789502016-03-23 Characterization and Localization of Citrullinated Proteoglycan Aggrecan in Human Articular Cartilage Glant, Tibor T. Ocsko, Timea Markovics, Adrienn Szekanecz, Zoltan Katz, Robert S. Rauch, Tibor A. Mikecz, Katalin PLoS One Research Article BACKGROUND: Rheumatoid arthritis (RA) is an autoimmune disease of the synovial joints. The autoimmune character of RA is underscored by prominent production of autoantibodies such as those against IgG (rheumatoid factor), and a broad array of joint tissue-specific and other endogenous citrullinated proteins. Anti-citrullinated protein antibodies (ACPA) can be detected in the sera and synovial fluids of RA patients and ACPA seropositivity is one of the diagnostic criteria of RA. Studies have demonstrated that RA T cells respond to citrullinated peptides (epitopes) of proteoglycan (PG) aggrecan, which is one of the most abundant macromolecules of articular cartilage. However, it is not known if the PG molecule is citrullinated in vivo in human cartilage, and if so, whether citrulline-containing neoepitopes of PG (CitPG) can contribute to autoimmunity in RA. METHODS: CitPG was detected in human cartilage extracts using ACPA+ RA sera in dot blot and Western blot. Citrullination status of in vitro citrullinated recombinant G1 domain of human PG (rhG1) was confirmed by antibody-based and chemical methods, and potential sites of citrullination in rhG1 were explored by molecular modeling. CitPG-specific serum autoantibodies were quantified by enzyme-linked immunosorbent assays, and CitPG was localized in osteoarthritic (OA) and RA cartilage using immunohistochemistry. FINDINGS: Sera from ACPA+ RA patients reacted with PG purified from normal human cartilage specimens. PG fragments (mainly those containing the G1 domain) from OA or RA cartilage extracts were recognized by ACPA+ sera but not by serum from ACPA- individuals. ACPA+ sera also reacted with in vitro citrullinated rhG1 and G3 domain-containing fragment(s) of PG. Molecular modeling suggested multiple sites of potential citrullination within the G1 domain. The immunohistochemical localization of CitPG was different in OA and RA cartilage. CONCLUSIONS: CitPG is a new member of citrullinated proteins identified in human joints. CitPG could be found in both normal and diseased cartilage specimens. Antibodies against CitPG may trigger or augment arthritis by forming immune complexes with this autoantigen in the joints of ACPA+ RA patients. Public Library of Science 2016-03-04 /pmc/articles/PMC4778950/ /pubmed/26943656 http://dx.doi.org/10.1371/journal.pone.0150784 Text en © 2016 Glant et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Glant, Tibor T.
Ocsko, Timea
Markovics, Adrienn
Szekanecz, Zoltan
Katz, Robert S.
Rauch, Tibor A.
Mikecz, Katalin
Characterization and Localization of Citrullinated Proteoglycan Aggrecan in Human Articular Cartilage
title Characterization and Localization of Citrullinated Proteoglycan Aggrecan in Human Articular Cartilage
title_full Characterization and Localization of Citrullinated Proteoglycan Aggrecan in Human Articular Cartilage
title_fullStr Characterization and Localization of Citrullinated Proteoglycan Aggrecan in Human Articular Cartilage
title_full_unstemmed Characterization and Localization of Citrullinated Proteoglycan Aggrecan in Human Articular Cartilage
title_short Characterization and Localization of Citrullinated Proteoglycan Aggrecan in Human Articular Cartilage
title_sort characterization and localization of citrullinated proteoglycan aggrecan in human articular cartilage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778950/
https://www.ncbi.nlm.nih.gov/pubmed/26943656
http://dx.doi.org/10.1371/journal.pone.0150784
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