Bone protection by inhibition of microRNA-182

Osteoclasts mediate bone disruption in a number of degenerative bone diseases. Here, the authors show that miR-182 regulates osteoclastogenesis via PKR and IFN-beta signaling, is correlated with rheumatoid arthritis, and that its ablation or inhibition is protective against bone erosion in mouse mod...

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Autores principales: Kazuki Inoue, Zhonghao Deng, Yufan Chen, Eugenia Giannopoulou, Ren Xu, Shiaoching Gong, Matthew B. Greenblatt, Lingegowda S. Mangala, Gabriel Lopez-Berestein, David G. Kirsch, Anil K. Sood, Liang Zhao, Baohong Zhao
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Lenguaje:EN
Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/b4b9145ef0434abfa54670e362c640db
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spelling oai:doaj.org-article:b4b9145ef0434abfa54670e362c640db2021-12-02T15:34:40ZBone protection by inhibition of microRNA-18210.1038/s41467-018-06446-02041-1723https://doaj.org/article/b4b9145ef0434abfa54670e362c640db2018-10-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-06446-0https://doaj.org/toc/2041-1723Osteoclasts mediate bone disruption in a number of degenerative bone diseases. Here, the authors show that miR-182 regulates osteoclastogenesis via PKR and IFN-beta signaling, is correlated with rheumatoid arthritis, and that its ablation or inhibition is protective against bone erosion in mouse models of osteoporosis or inflammatory arthritis.Kazuki InoueZhonghao DengYufan ChenEugenia GiannopoulouRen XuShiaoching GongMatthew B. GreenblattLingegowda S. MangalaGabriel Lopez-BeresteinDavid G. KirschAnil K. SoodLiang ZhaoBaohong ZhaoNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-17 (2018)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Kazuki Inoue
Zhonghao Deng
Yufan Chen
Eugenia Giannopoulou
Ren Xu
Shiaoching Gong
Matthew B. Greenblatt
Lingegowda S. Mangala
Gabriel Lopez-Berestein
David G. Kirsch
Anil K. Sood
Liang Zhao
Baohong Zhao
Bone protection by inhibition of microRNA-182
description Osteoclasts mediate bone disruption in a number of degenerative bone diseases. Here, the authors show that miR-182 regulates osteoclastogenesis via PKR and IFN-beta signaling, is correlated with rheumatoid arthritis, and that its ablation or inhibition is protective against bone erosion in mouse models of osteoporosis or inflammatory arthritis.
format article
author Kazuki Inoue
Zhonghao Deng
Yufan Chen
Eugenia Giannopoulou
Ren Xu
Shiaoching Gong
Matthew B. Greenblatt
Lingegowda S. Mangala
Gabriel Lopez-Berestein
David G. Kirsch
Anil K. Sood
Liang Zhao
Baohong Zhao
author_facet Kazuki Inoue
Zhonghao Deng
Yufan Chen
Eugenia Giannopoulou
Ren Xu
Shiaoching Gong
Matthew B. Greenblatt
Lingegowda S. Mangala
Gabriel Lopez-Berestein
David G. Kirsch
Anil K. Sood
Liang Zhao
Baohong Zhao
author_sort Kazuki Inoue
title Bone protection by inhibition of microRNA-182
title_short Bone protection by inhibition of microRNA-182
title_full Bone protection by inhibition of microRNA-182
title_fullStr Bone protection by inhibition of microRNA-182
title_full_unstemmed Bone protection by inhibition of microRNA-182
title_sort bone protection by inhibition of microrna-182
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/b4b9145ef0434abfa54670e362c640db
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