Cargando…

The microRNAs miR-204 and miR-211 maintain joint homeostasis and protect against osteoarthritis progression

Osteoarthritis (OA) is a common, painful disease. Currently OA is incurable, and its etiology largely unknown, partly due to limited understanding of OA as a whole-joint disease. Here we report that two homologous microRNAs, miR-204 and miR-211, maintain joint homeostasis to suppress OA pathogenesis...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Jian, Zhao, Lan, Fan, Yunshan, Liao, Lifan, Ma, Peter X., Xiao, Guozhi, Chen, Di
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599052/
https://www.ncbi.nlm.nih.gov/pubmed/31253842
http://dx.doi.org/10.1038/s41467-019-10753-5
_version_ 1783430882153988096
author Huang, Jian
Zhao, Lan
Fan, Yunshan
Liao, Lifan
Ma, Peter X.
Xiao, Guozhi
Chen, Di
author_facet Huang, Jian
Zhao, Lan
Fan, Yunshan
Liao, Lifan
Ma, Peter X.
Xiao, Guozhi
Chen, Di
author_sort Huang, Jian
collection PubMed
description Osteoarthritis (OA) is a common, painful disease. Currently OA is incurable, and its etiology largely unknown, partly due to limited understanding of OA as a whole-joint disease. Here we report that two homologous microRNAs, miR-204 and miR-211, maintain joint homeostasis to suppress OA pathogenesis. Specific knockout of miR-204/-211 in mesenchymal progenitor cells (MPCs) results in Runx2 accumulation in multi-type joint cells, causing whole-joint degeneration. Specifically, miR-204/-211 loss-of-function induces matrix-degrading proteases in articular chondrocytes and synoviocytes, stimulating articular cartilage destruction. Moreover, miR-204/-211 ablation enhances NGF expression in a Runx2-dependent manner, and thus hyper-activates Akt signaling and MPC proliferation, underlying multiplex non-cartilaginous OA conditions including synovial hyperplasia, osteophyte outgrowth and subchondral sclerosis. Importantly, miR-204/-211-deficiency-induced OA is largely rescued by Runx2 insufficiency, confirming the miR-204/-211-Runx2 axis. Further, intraarticular administration of miR-204-expressing adeno-associated virus significantly decelerates OA progression. Collectively, miR-204/-211 are essential in maintaining healthy homeostasis of mesenchymal joint cells to counteract OA pathogenesis.
format Online
Article
Text
id pubmed-6599052
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-65990522019-07-01 The microRNAs miR-204 and miR-211 maintain joint homeostasis and protect against osteoarthritis progression Huang, Jian Zhao, Lan Fan, Yunshan Liao, Lifan Ma, Peter X. Xiao, Guozhi Chen, Di Nat Commun Article Osteoarthritis (OA) is a common, painful disease. Currently OA is incurable, and its etiology largely unknown, partly due to limited understanding of OA as a whole-joint disease. Here we report that two homologous microRNAs, miR-204 and miR-211, maintain joint homeostasis to suppress OA pathogenesis. Specific knockout of miR-204/-211 in mesenchymal progenitor cells (MPCs) results in Runx2 accumulation in multi-type joint cells, causing whole-joint degeneration. Specifically, miR-204/-211 loss-of-function induces matrix-degrading proteases in articular chondrocytes and synoviocytes, stimulating articular cartilage destruction. Moreover, miR-204/-211 ablation enhances NGF expression in a Runx2-dependent manner, and thus hyper-activates Akt signaling and MPC proliferation, underlying multiplex non-cartilaginous OA conditions including synovial hyperplasia, osteophyte outgrowth and subchondral sclerosis. Importantly, miR-204/-211-deficiency-induced OA is largely rescued by Runx2 insufficiency, confirming the miR-204/-211-Runx2 axis. Further, intraarticular administration of miR-204-expressing adeno-associated virus significantly decelerates OA progression. Collectively, miR-204/-211 are essential in maintaining healthy homeostasis of mesenchymal joint cells to counteract OA pathogenesis. Nature Publishing Group UK 2019-06-28 /pmc/articles/PMC6599052/ /pubmed/31253842 http://dx.doi.org/10.1038/s41467-019-10753-5 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Huang, Jian
Zhao, Lan
Fan, Yunshan
Liao, Lifan
Ma, Peter X.
Xiao, Guozhi
Chen, Di
The microRNAs miR-204 and miR-211 maintain joint homeostasis and protect against osteoarthritis progression
title The microRNAs miR-204 and miR-211 maintain joint homeostasis and protect against osteoarthritis progression
title_full The microRNAs miR-204 and miR-211 maintain joint homeostasis and protect against osteoarthritis progression
title_fullStr The microRNAs miR-204 and miR-211 maintain joint homeostasis and protect against osteoarthritis progression
title_full_unstemmed The microRNAs miR-204 and miR-211 maintain joint homeostasis and protect against osteoarthritis progression
title_short The microRNAs miR-204 and miR-211 maintain joint homeostasis and protect against osteoarthritis progression
title_sort micrornas mir-204 and mir-211 maintain joint homeostasis and protect against osteoarthritis progression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599052/
https://www.ncbi.nlm.nih.gov/pubmed/31253842
http://dx.doi.org/10.1038/s41467-019-10753-5
work_keys_str_mv AT huangjian themicrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT zhaolan themicrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT fanyunshan themicrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT liaolifan themicrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT mapeterx themicrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT xiaoguozhi themicrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT chendi themicrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT huangjian micrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT zhaolan micrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT fanyunshan micrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT liaolifan micrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT mapeterx micrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT xiaoguozhi micrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression
AT chendi micrornasmir204andmir211maintainjointhomeostasisandprotectagainstosteoarthritisprogression