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Complement Expression and Activation in Osteoarthritis Joint Compartments

OBJECTIVE: To investigate complement(C) factors(F) and their activation fragments expression in OA joint tissues. DESIGN: Immunohistochemistry and quantitative imaging were performed to analyze C3, C4, and CF (factor) B expression on osteochondral biopsies (43 patients) collected during arthroplasty...

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Autores principales: Assirelli, Elisa, Pulsatelli, Lia, Dolzani, Paolo, Mariani, Erminia, Lisignoli, Gina, Addimanda, Olga, Meliconi, Riccardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658426/
https://www.ncbi.nlm.nih.gov/pubmed/33193305
http://dx.doi.org/10.3389/fimmu.2020.535010
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author Assirelli, Elisa
Pulsatelli, Lia
Dolzani, Paolo
Mariani, Erminia
Lisignoli, Gina
Addimanda, Olga
Meliconi, Riccardo
author_facet Assirelli, Elisa
Pulsatelli, Lia
Dolzani, Paolo
Mariani, Erminia
Lisignoli, Gina
Addimanda, Olga
Meliconi, Riccardo
author_sort Assirelli, Elisa
collection PubMed
description OBJECTIVE: To investigate complement(C) factors(F) and their activation fragments expression in OA joint tissues. DESIGN: Immunohistochemistry and quantitative imaging were performed to analyze C3, C4, and CF (factor) B expression on osteochondral biopsies (43 patients) collected during arthroplasty. Isolated chondrocytes and synoviocytes, cartilage and synovial tissues obtained from surgical specimens of OA patients (15 patients) were cultured with or without IL-1β. Real time PCR for CFB, C3, and C4 was performed. Culture supernatants were analyzed for C3a, C5a, CFBa, and terminal complement complex (TCC) production. RESULTS: In osteochondral biopsies, C factor expression was located in bone marrow, in a few subchondral bone cells and chondrocytes. C3 was the most expressed while factor C4 was the least expressed factor. Gene expression showed that all C factors analyzed were expressed both in chondrocytes and synoviocytes. In chondrocyte cultures and cartilage explants, CFB expression was significantly higher than C3 and C4. Furthermore, CFB, but not C3 and C4 expression was significantly induced by IL-1β. As to C activation factors, C3a was the most produced and CFBa was induced by IL-1β in synovial tissue. TCC production was undetectable in isolated chondrocytes and synoviocytes cell culture supernatants, whereas it was significantly augmented in cartilage explants. CONCLUSION: C factors were locally produced and activated in OA joint with the contribution of all tissues (cartilage, bone, and synovium). Our results support the involvement of innate immunity in OA and suggest an association between some C alternative pathway component and joint inflammation.
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spelling pubmed-76584262020-11-13 Complement Expression and Activation in Osteoarthritis Joint Compartments Assirelli, Elisa Pulsatelli, Lia Dolzani, Paolo Mariani, Erminia Lisignoli, Gina Addimanda, Olga Meliconi, Riccardo Front Immunol Immunology OBJECTIVE: To investigate complement(C) factors(F) and their activation fragments expression in OA joint tissues. DESIGN: Immunohistochemistry and quantitative imaging were performed to analyze C3, C4, and CF (factor) B expression on osteochondral biopsies (43 patients) collected during arthroplasty. Isolated chondrocytes and synoviocytes, cartilage and synovial tissues obtained from surgical specimens of OA patients (15 patients) were cultured with or without IL-1β. Real time PCR for CFB, C3, and C4 was performed. Culture supernatants were analyzed for C3a, C5a, CFBa, and terminal complement complex (TCC) production. RESULTS: In osteochondral biopsies, C factor expression was located in bone marrow, in a few subchondral bone cells and chondrocytes. C3 was the most expressed while factor C4 was the least expressed factor. Gene expression showed that all C factors analyzed were expressed both in chondrocytes and synoviocytes. In chondrocyte cultures and cartilage explants, CFB expression was significantly higher than C3 and C4. Furthermore, CFB, but not C3 and C4 expression was significantly induced by IL-1β. As to C activation factors, C3a was the most produced and CFBa was induced by IL-1β in synovial tissue. TCC production was undetectable in isolated chondrocytes and synoviocytes cell culture supernatants, whereas it was significantly augmented in cartilage explants. CONCLUSION: C factors were locally produced and activated in OA joint with the contribution of all tissues (cartilage, bone, and synovium). Our results support the involvement of innate immunity in OA and suggest an association between some C alternative pathway component and joint inflammation. Frontiers Media S.A. 2020-10-29 /pmc/articles/PMC7658426/ /pubmed/33193305 http://dx.doi.org/10.3389/fimmu.2020.535010 Text en Copyright © 2020 Assirelli, Pulsatelli, Dolzani, Mariani, Lisignoli, Addimanda and Meliconi http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Assirelli, Elisa
Pulsatelli, Lia
Dolzani, Paolo
Mariani, Erminia
Lisignoli, Gina
Addimanda, Olga
Meliconi, Riccardo
Complement Expression and Activation in Osteoarthritis Joint Compartments
title Complement Expression and Activation in Osteoarthritis Joint Compartments
title_full Complement Expression and Activation in Osteoarthritis Joint Compartments
title_fullStr Complement Expression and Activation in Osteoarthritis Joint Compartments
title_full_unstemmed Complement Expression and Activation in Osteoarthritis Joint Compartments
title_short Complement Expression and Activation in Osteoarthritis Joint Compartments
title_sort complement expression and activation in osteoarthritis joint compartments
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658426/
https://www.ncbi.nlm.nih.gov/pubmed/33193305
http://dx.doi.org/10.3389/fimmu.2020.535010
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