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Characterization of miR-335-5p and miR-335-3p in human osteoarthritic tissues

OBJECTIVE: We aimed to characterize the expression patterns, gene targets, and functional effects of miR-335-5p and miR-335-3p among seven primary human knee and hip osteoarthritic tissue types. METHODS: We collected synovial fluid, subchondral bone, articular cartilage, synovium, meniscus/labrum, i...

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Autores principales: Wilson, Thomas G., Baghel, Madhu, Kaur, Navdeep, Moutzouros, Vasilios, Davis, Jason, Ali, Shabana Amanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273720/
https://www.ncbi.nlm.nih.gov/pubmed/37328905
http://dx.doi.org/10.1186/s13075-023-03088-6
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author Wilson, Thomas G.
Baghel, Madhu
Kaur, Navdeep
Moutzouros, Vasilios
Davis, Jason
Ali, Shabana Amanda
author_facet Wilson, Thomas G.
Baghel, Madhu
Kaur, Navdeep
Moutzouros, Vasilios
Davis, Jason
Ali, Shabana Amanda
author_sort Wilson, Thomas G.
collection PubMed
description OBJECTIVE: We aimed to characterize the expression patterns, gene targets, and functional effects of miR-335-5p and miR-335-3p among seven primary human knee and hip osteoarthritic tissue types. METHODS: We collected synovial fluid, subchondral bone, articular cartilage, synovium, meniscus/labrum, infrapatellar/acetabular fat, anterior cruciate ligament/ligamentum teres, and vastus medialis oblique/quadratus femoris muscle (n = 7–20) from surgical patients with early- or late-stage osteoarthritis (OA) and quantified miR-335-5p and miR-335-3p expression by real-time PCR. Predicted gene targets were measured in knee OA infrapatellar fat following miRNA inhibitor transfection (n = 3), and prioritized gene targets were validated following miRNA inhibitor and mimic transfection (n = 6). Following pathway analyses, we performed Oil-Red-O staining to assess changes in total lipid content in infrapatellar fat. RESULTS: Showing a 227-fold increase in knee OA infrapatellar fat (the highest expressing tissue) versus meniscus (the lowest expressing tissue), miR-335-5p was more abundant than miR-335-3p (92-fold increase). MiR-335-5p showed higher expression across knee tissues versus hip tissues, and in late-stage versus early-stage knee OA fat. Exploring candidate genes, VCAM1 and MMP13 were identified as putative direct targets of miR-335-5p and miR-335-3p, respectively, showing downregulation with miRNA mimic transfection. Exploring candidate pathways, predicted miR-335-5p gene targets were enriched in a canonical adipogenesis network (p = 2.1e − 5). Modulation of miR-335-5p in late-stage knee OA fat showed an inverse relationship to total lipid content. CONCLUSION: Our data suggest both miR-335-5p and miR-335-3p regulate gene targets in late-stage knee OA infrapatellar fat, though miR-335-5p appears to be more prominent, with tissue-, joint-, and stage-specific effects. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-023-03088-6.
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spelling pubmed-102737202023-06-17 Characterization of miR-335-5p and miR-335-3p in human osteoarthritic tissues Wilson, Thomas G. Baghel, Madhu Kaur, Navdeep Moutzouros, Vasilios Davis, Jason Ali, Shabana Amanda Arthritis Res Ther Research OBJECTIVE: We aimed to characterize the expression patterns, gene targets, and functional effects of miR-335-5p and miR-335-3p among seven primary human knee and hip osteoarthritic tissue types. METHODS: We collected synovial fluid, subchondral bone, articular cartilage, synovium, meniscus/labrum, infrapatellar/acetabular fat, anterior cruciate ligament/ligamentum teres, and vastus medialis oblique/quadratus femoris muscle (n = 7–20) from surgical patients with early- or late-stage osteoarthritis (OA) and quantified miR-335-5p and miR-335-3p expression by real-time PCR. Predicted gene targets were measured in knee OA infrapatellar fat following miRNA inhibitor transfection (n = 3), and prioritized gene targets were validated following miRNA inhibitor and mimic transfection (n = 6). Following pathway analyses, we performed Oil-Red-O staining to assess changes in total lipid content in infrapatellar fat. RESULTS: Showing a 227-fold increase in knee OA infrapatellar fat (the highest expressing tissue) versus meniscus (the lowest expressing tissue), miR-335-5p was more abundant than miR-335-3p (92-fold increase). MiR-335-5p showed higher expression across knee tissues versus hip tissues, and in late-stage versus early-stage knee OA fat. Exploring candidate genes, VCAM1 and MMP13 were identified as putative direct targets of miR-335-5p and miR-335-3p, respectively, showing downregulation with miRNA mimic transfection. Exploring candidate pathways, predicted miR-335-5p gene targets were enriched in a canonical adipogenesis network (p = 2.1e − 5). Modulation of miR-335-5p in late-stage knee OA fat showed an inverse relationship to total lipid content. CONCLUSION: Our data suggest both miR-335-5p and miR-335-3p regulate gene targets in late-stage knee OA infrapatellar fat, though miR-335-5p appears to be more prominent, with tissue-, joint-, and stage-specific effects. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-023-03088-6. BioMed Central 2023-06-16 2023 /pmc/articles/PMC10273720/ /pubmed/37328905 http://dx.doi.org/10.1186/s13075-023-03088-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wilson, Thomas G.
Baghel, Madhu
Kaur, Navdeep
Moutzouros, Vasilios
Davis, Jason
Ali, Shabana Amanda
Characterization of miR-335-5p and miR-335-3p in human osteoarthritic tissues
title Characterization of miR-335-5p and miR-335-3p in human osteoarthritic tissues
title_full Characterization of miR-335-5p and miR-335-3p in human osteoarthritic tissues
title_fullStr Characterization of miR-335-5p and miR-335-3p in human osteoarthritic tissues
title_full_unstemmed Characterization of miR-335-5p and miR-335-3p in human osteoarthritic tissues
title_short Characterization of miR-335-5p and miR-335-3p in human osteoarthritic tissues
title_sort characterization of mir-335-5p and mir-335-3p in human osteoarthritic tissues
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273720/
https://www.ncbi.nlm.nih.gov/pubmed/37328905
http://dx.doi.org/10.1186/s13075-023-03088-6
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