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HuR-mediated nucleocytoplasmic translocation of HOTAIR relieves its inhibition of osteogenic differentiation and promotes bone formation

Bone marrow mesenchymal stem cell (BMSC) osteogenic differentiation and osteoblast function play critical roles in bone formation, which is a highly regulated process. Long noncoding RNAs (lncRNAs) perform diverse functions in a variety of biological processes, including BMSC osteogenic differentiat...

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Autores principales: Li, Yuheng, Sun, Weijia, Li, Jianwei, Du, Ruikai, Xing, Wenjuan, Yuan, Xinxin, Zhong, Guohui, Zhao, Dingsheng, Liu, Zizhong, Jin, Xiaoyan, Pan, Junjie, Li, Youyou, Li, Qi, Kan, Guanghan, Han, Xuan, Ling, Shukuan, Sun, Xiqing, Li, Yingxian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593784/
https://www.ncbi.nlm.nih.gov/pubmed/37872163
http://dx.doi.org/10.1038/s41413-023-00289-2
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author Li, Yuheng
Sun, Weijia
Li, Jianwei
Du, Ruikai
Xing, Wenjuan
Yuan, Xinxin
Zhong, Guohui
Zhao, Dingsheng
Liu, Zizhong
Jin, Xiaoyan
Pan, Junjie
Li, Youyou
Li, Qi
Kan, Guanghan
Han, Xuan
Ling, Shukuan
Sun, Xiqing
Li, Yingxian
author_facet Li, Yuheng
Sun, Weijia
Li, Jianwei
Du, Ruikai
Xing, Wenjuan
Yuan, Xinxin
Zhong, Guohui
Zhao, Dingsheng
Liu, Zizhong
Jin, Xiaoyan
Pan, Junjie
Li, Youyou
Li, Qi
Kan, Guanghan
Han, Xuan
Ling, Shukuan
Sun, Xiqing
Li, Yingxian
author_sort Li, Yuheng
collection PubMed
description Bone marrow mesenchymal stem cell (BMSC) osteogenic differentiation and osteoblast function play critical roles in bone formation, which is a highly regulated process. Long noncoding RNAs (lncRNAs) perform diverse functions in a variety of biological processes, including BMSC osteogenic differentiation. Although several studies have reported that HOX transcript antisense RNA (HOTAIR) is involved in BMSC osteogenic differentiation, its effect on bone formation in vivo remains unclear. Here, by constructing transgenic mice with BMSC (Prx1-HOTAIR)- and osteoblast (Bglap-HOTAIR)-specific overexpression of HOTAIR, we found that Prx1-HOTAIR and Bglap-HOTAIR transgenic mice show different bone phenotypes in vivo. Specifically, Prx1-HOTAIR mice showed delayed bone formation, while Bglap-HOTAIR mice showed increased bone formation. HOTAIR inhibits BMSC osteogenic differentiation but promotes osteoblast function in vitro. Furthermore, we identified that HOTAIR is mainly located in the nucleus of BMSCs and in the cytoplasm of osteoblasts. HOTAIR displays a nucleocytoplasmic translocation pattern during BMSC osteogenic differentiation. We first identified that the RNA-binding protein human antigen R (HuR) is responsible for HOTAIR nucleocytoplasmic translocation. HOTAIR is essential for osteoblast function, and cytoplasmic HOTAIR binds to miR-214 and acts as a ceRNA to increase Atf4 protein levels and osteoblast function. Bglap-HOTAIR mice, but not Prx1-HOTAIR mice, showed alleviation of bone loss induced by unloading. This study reveals the importance of temporal and spatial regulation of HOTAIR in BMSC osteogenic differentiation and bone formation, which provides new insights into precise regulation as a target for bone loss.
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spelling pubmed-105937842023-10-25 HuR-mediated nucleocytoplasmic translocation of HOTAIR relieves its inhibition of osteogenic differentiation and promotes bone formation Li, Yuheng Sun, Weijia Li, Jianwei Du, Ruikai Xing, Wenjuan Yuan, Xinxin Zhong, Guohui Zhao, Dingsheng Liu, Zizhong Jin, Xiaoyan Pan, Junjie Li, Youyou Li, Qi Kan, Guanghan Han, Xuan Ling, Shukuan Sun, Xiqing Li, Yingxian Bone Res Article Bone marrow mesenchymal stem cell (BMSC) osteogenic differentiation and osteoblast function play critical roles in bone formation, which is a highly regulated process. Long noncoding RNAs (lncRNAs) perform diverse functions in a variety of biological processes, including BMSC osteogenic differentiation. Although several studies have reported that HOX transcript antisense RNA (HOTAIR) is involved in BMSC osteogenic differentiation, its effect on bone formation in vivo remains unclear. Here, by constructing transgenic mice with BMSC (Prx1-HOTAIR)- and osteoblast (Bglap-HOTAIR)-specific overexpression of HOTAIR, we found that Prx1-HOTAIR and Bglap-HOTAIR transgenic mice show different bone phenotypes in vivo. Specifically, Prx1-HOTAIR mice showed delayed bone formation, while Bglap-HOTAIR mice showed increased bone formation. HOTAIR inhibits BMSC osteogenic differentiation but promotes osteoblast function in vitro. Furthermore, we identified that HOTAIR is mainly located in the nucleus of BMSCs and in the cytoplasm of osteoblasts. HOTAIR displays a nucleocytoplasmic translocation pattern during BMSC osteogenic differentiation. We first identified that the RNA-binding protein human antigen R (HuR) is responsible for HOTAIR nucleocytoplasmic translocation. HOTAIR is essential for osteoblast function, and cytoplasmic HOTAIR binds to miR-214 and acts as a ceRNA to increase Atf4 protein levels and osteoblast function. Bglap-HOTAIR mice, but not Prx1-HOTAIR mice, showed alleviation of bone loss induced by unloading. This study reveals the importance of temporal and spatial regulation of HOTAIR in BMSC osteogenic differentiation and bone formation, which provides new insights into precise regulation as a target for bone loss. Nature Publishing Group UK 2023-10-23 /pmc/articles/PMC10593784/ /pubmed/37872163 http://dx.doi.org/10.1038/s41413-023-00289-2 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Yuheng
Sun, Weijia
Li, Jianwei
Du, Ruikai
Xing, Wenjuan
Yuan, Xinxin
Zhong, Guohui
Zhao, Dingsheng
Liu, Zizhong
Jin, Xiaoyan
Pan, Junjie
Li, Youyou
Li, Qi
Kan, Guanghan
Han, Xuan
Ling, Shukuan
Sun, Xiqing
Li, Yingxian
HuR-mediated nucleocytoplasmic translocation of HOTAIR relieves its inhibition of osteogenic differentiation and promotes bone formation
title HuR-mediated nucleocytoplasmic translocation of HOTAIR relieves its inhibition of osteogenic differentiation and promotes bone formation
title_full HuR-mediated nucleocytoplasmic translocation of HOTAIR relieves its inhibition of osteogenic differentiation and promotes bone formation
title_fullStr HuR-mediated nucleocytoplasmic translocation of HOTAIR relieves its inhibition of osteogenic differentiation and promotes bone formation
title_full_unstemmed HuR-mediated nucleocytoplasmic translocation of HOTAIR relieves its inhibition of osteogenic differentiation and promotes bone formation
title_short HuR-mediated nucleocytoplasmic translocation of HOTAIR relieves its inhibition of osteogenic differentiation and promotes bone formation
title_sort hur-mediated nucleocytoplasmic translocation of hotair relieves its inhibition of osteogenic differentiation and promotes bone formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593784/
https://www.ncbi.nlm.nih.gov/pubmed/37872163
http://dx.doi.org/10.1038/s41413-023-00289-2
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