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Proteomic comparison of osteoarthritic and reference human menisci using data-independent acquisition mass spectrometry

OBJECTIVE: Recent research in knee osteoarthritis (OA) highlights the role of the meniscus in OA pathology. Our aim was to compare the proteomes of medial and lateral menisci from end-stage medial compartment knee OA patients, with reference menisci from knee-healthy deceased donors, using mass spec...

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Autores principales: Folkesson, E., Turkiewicz, A., Ali, N., Rydén, M., Hughes, H.V., Tjörnstrand, J., Önnerfjord, P., Englund, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: W.B. Saunders For The Osteoarthritis Research Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397514/
https://www.ncbi.nlm.nih.gov/pubmed/32407894
http://dx.doi.org/10.1016/j.joca.2020.05.001
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author Folkesson, E.
Turkiewicz, A.
Ali, N.
Rydén, M.
Hughes, H.V.
Tjörnstrand, J.
Önnerfjord, P.
Englund, M.
author_facet Folkesson, E.
Turkiewicz, A.
Ali, N.
Rydén, M.
Hughes, H.V.
Tjörnstrand, J.
Önnerfjord, P.
Englund, M.
author_sort Folkesson, E.
collection PubMed
description OBJECTIVE: Recent research in knee osteoarthritis (OA) highlights the role of the meniscus in OA pathology. Our aim was to compare the proteomes of medial and lateral menisci from end-stage medial compartment knee OA patients, with reference menisci from knee-healthy deceased donors, using mass spectrometry. DESIGN: Tissue plugs of Ø3 mm were obtained from the posterior horns of the lateral and medial menisci from one knee of 10 knee-healthy deceased donors and 10 patients undergoing knee replacement. Proteins were extracted and prepared for mass spectrometric analysis. Statistical analysis was conducted on abundance data that was log(2)-transformed, using a linear mixed effects model and evaluated using pathway analysis. RESULTS: We identified a total of 835 proteins in all samples, of which 331 were included in the statistical analysis. The largest differences could be seen between the medial menisci from OA patients and references, with most proteins showing higher intensities in the medial menisci from OA patients. Several matrix proteins, e.g., matrix metalloproteinase 3 (MMP3) (4.3 times higher values [95%CI 1.8, 10.6]), TIMP1 (3.5 [1.4, 8.5]), asporin (4.1 [1.7, 10.0]) and versican (4.4 [1.8, 10.9]), all showed higher abundance in medial menisci from OA patients compared to medial reference menisci. OA medial menisci also showed increased activation of several pathways involved in inflammation. CONCLUSION: An increase in protein abundance for proteins such as MMP and TIMP1 in the medial menisci from OA patients suggests simultaneous activation of both catabolic and anabolic processes that warrants further attention.
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spelling pubmed-73975142020-08-06 Proteomic comparison of osteoarthritic and reference human menisci using data-independent acquisition mass spectrometry Folkesson, E. Turkiewicz, A. Ali, N. Rydén, M. Hughes, H.V. Tjörnstrand, J. Önnerfjord, P. Englund, M. Osteoarthritis Cartilage Article OBJECTIVE: Recent research in knee osteoarthritis (OA) highlights the role of the meniscus in OA pathology. Our aim was to compare the proteomes of medial and lateral menisci from end-stage medial compartment knee OA patients, with reference menisci from knee-healthy deceased donors, using mass spectrometry. DESIGN: Tissue plugs of Ø3 mm were obtained from the posterior horns of the lateral and medial menisci from one knee of 10 knee-healthy deceased donors and 10 patients undergoing knee replacement. Proteins were extracted and prepared for mass spectrometric analysis. Statistical analysis was conducted on abundance data that was log(2)-transformed, using a linear mixed effects model and evaluated using pathway analysis. RESULTS: We identified a total of 835 proteins in all samples, of which 331 were included in the statistical analysis. The largest differences could be seen between the medial menisci from OA patients and references, with most proteins showing higher intensities in the medial menisci from OA patients. Several matrix proteins, e.g., matrix metalloproteinase 3 (MMP3) (4.3 times higher values [95%CI 1.8, 10.6]), TIMP1 (3.5 [1.4, 8.5]), asporin (4.1 [1.7, 10.0]) and versican (4.4 [1.8, 10.9]), all showed higher abundance in medial menisci from OA patients compared to medial reference menisci. OA medial menisci also showed increased activation of several pathways involved in inflammation. CONCLUSION: An increase in protein abundance for proteins such as MMP and TIMP1 in the medial menisci from OA patients suggests simultaneous activation of both catabolic and anabolic processes that warrants further attention. W.B. Saunders For The Osteoarthritis Research Society 2020-08 /pmc/articles/PMC7397514/ /pubmed/32407894 http://dx.doi.org/10.1016/j.joca.2020.05.001 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Folkesson, E.
Turkiewicz, A.
Ali, N.
Rydén, M.
Hughes, H.V.
Tjörnstrand, J.
Önnerfjord, P.
Englund, M.
Proteomic comparison of osteoarthritic and reference human menisci using data-independent acquisition mass spectrometry
title Proteomic comparison of osteoarthritic and reference human menisci using data-independent acquisition mass spectrometry
title_full Proteomic comparison of osteoarthritic and reference human menisci using data-independent acquisition mass spectrometry
title_fullStr Proteomic comparison of osteoarthritic and reference human menisci using data-independent acquisition mass spectrometry
title_full_unstemmed Proteomic comparison of osteoarthritic and reference human menisci using data-independent acquisition mass spectrometry
title_short Proteomic comparison of osteoarthritic and reference human menisci using data-independent acquisition mass spectrometry
title_sort proteomic comparison of osteoarthritic and reference human menisci using data-independent acquisition mass spectrometry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397514/
https://www.ncbi.nlm.nih.gov/pubmed/32407894
http://dx.doi.org/10.1016/j.joca.2020.05.001
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