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Noncoding RNAs in subchondral bone osteoclast function and their therapeutic potential for osteoarthritis

Osteoclasts are the only cells that perform bone resorption. Noncoding RNAs (ncRNAs) are crucial epigenetic regulators of osteoclast biological behaviors ranging from osteoclast differentiation to bone resorption. The main ncRNAs, including miRNAs, circRNAs, and lncRNAs, compose an intricate network...

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Autores principales: Duan, Li, Liang, Yujie, Xu, Xiao, Wang, Jifeng, Li, Xingfu, Sun, Deshun, Deng, Zhiqin, Li, Wencui, Wang, Daping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690185/
https://www.ncbi.nlm.nih.gov/pubmed/33239099
http://dx.doi.org/10.1186/s13075-020-02374-x
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author Duan, Li
Liang, Yujie
Xu, Xiao
Wang, Jifeng
Li, Xingfu
Sun, Deshun
Deng, Zhiqin
Li, Wencui
Wang, Daping
author_facet Duan, Li
Liang, Yujie
Xu, Xiao
Wang, Jifeng
Li, Xingfu
Sun, Deshun
Deng, Zhiqin
Li, Wencui
Wang, Daping
author_sort Duan, Li
collection PubMed
description Osteoclasts are the only cells that perform bone resorption. Noncoding RNAs (ncRNAs) are crucial epigenetic regulators of osteoclast biological behaviors ranging from osteoclast differentiation to bone resorption. The main ncRNAs, including miRNAs, circRNAs, and lncRNAs, compose an intricate network that influences gene transcription processes related to osteoclast biological activity. Accumulating evidence suggests that abnormal osteoclast activity leads to the disturbance of subchondral bone remodeling, thus initiating osteoarthritis (OA), a prevalent joint disease characterized mainly by cartilage degradation and subchondral bone remodeling imbalance. In this review, we delineate three types of ncRNAs and discuss their related complex molecular signaling pathways associated with osteoclast function during bone resorption. We specifically focused on the involvement of noncoding RNAs in subchondral bone remodeling, which participate in the degradation of the osteochondral unit during OA progression. We also discussed exosomes as ncRNA carriers during the bone remodeling process. A better understanding of the roles of ncRNAs in osteoclast biological behaviors will contribute to the treatment of bone resorption-related skeletal diseases such as OA.
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spelling pubmed-76901852020-11-30 Noncoding RNAs in subchondral bone osteoclast function and their therapeutic potential for osteoarthritis Duan, Li Liang, Yujie Xu, Xiao Wang, Jifeng Li, Xingfu Sun, Deshun Deng, Zhiqin Li, Wencui Wang, Daping Arthritis Res Ther Review Osteoclasts are the only cells that perform bone resorption. Noncoding RNAs (ncRNAs) are crucial epigenetic regulators of osteoclast biological behaviors ranging from osteoclast differentiation to bone resorption. The main ncRNAs, including miRNAs, circRNAs, and lncRNAs, compose an intricate network that influences gene transcription processes related to osteoclast biological activity. Accumulating evidence suggests that abnormal osteoclast activity leads to the disturbance of subchondral bone remodeling, thus initiating osteoarthritis (OA), a prevalent joint disease characterized mainly by cartilage degradation and subchondral bone remodeling imbalance. In this review, we delineate three types of ncRNAs and discuss their related complex molecular signaling pathways associated with osteoclast function during bone resorption. We specifically focused on the involvement of noncoding RNAs in subchondral bone remodeling, which participate in the degradation of the osteochondral unit during OA progression. We also discussed exosomes as ncRNA carriers during the bone remodeling process. A better understanding of the roles of ncRNAs in osteoclast biological behaviors will contribute to the treatment of bone resorption-related skeletal diseases such as OA. BioMed Central 2020-11-25 2020 /pmc/articles/PMC7690185/ /pubmed/33239099 http://dx.doi.org/10.1186/s13075-020-02374-x Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://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 Review
Duan, Li
Liang, Yujie
Xu, Xiao
Wang, Jifeng
Li, Xingfu
Sun, Deshun
Deng, Zhiqin
Li, Wencui
Wang, Daping
Noncoding RNAs in subchondral bone osteoclast function and their therapeutic potential for osteoarthritis
title Noncoding RNAs in subchondral bone osteoclast function and their therapeutic potential for osteoarthritis
title_full Noncoding RNAs in subchondral bone osteoclast function and their therapeutic potential for osteoarthritis
title_fullStr Noncoding RNAs in subchondral bone osteoclast function and their therapeutic potential for osteoarthritis
title_full_unstemmed Noncoding RNAs in subchondral bone osteoclast function and their therapeutic potential for osteoarthritis
title_short Noncoding RNAs in subchondral bone osteoclast function and their therapeutic potential for osteoarthritis
title_sort noncoding rnas in subchondral bone osteoclast function and their therapeutic potential for osteoarthritis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690185/
https://www.ncbi.nlm.nih.gov/pubmed/33239099
http://dx.doi.org/10.1186/s13075-020-02374-x
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