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| Auteurs principaux: | , , , , , , , , , , , , |
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| Format: | Artículo Open Access |
| Publié: |
Wiley
2024
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| Sujets: | |
| Accès en ligne: | https://onlinelibrary.wiley.com/doi/10.1111/cpr.13607 |
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| _version_ | 1867012806830718976 |
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| author | Haoqing Yang Wanqing Wang Huina Liu Chen Zhang Yangyang Cao Lujue Long Xiao Han Yuejun Wang Fei Yan Guoqing Li Mengyuan Zhu Luyuan Jin Zhipeng Fan |
| author_facet | Haoqing Yang Wanqing Wang Huina Liu Chen Zhang Yangyang Cao Lujue Long Xiao Han Yuejun Wang Fei Yan Guoqing Li Mengyuan Zhu Luyuan Jin Zhipeng Fan Haoqing Yang Wanqing Wang Huina Liu Chen Zhang Yangyang Cao Lujue Long Xiao Han Yuejun Wang Fei Yan Guoqing Li Mengyuan Zhu Luyuan Jin Zhipeng Fan |
| collection | Wiley Open Access |
| contents | miR615‐3p inhibited FBLN1 and osteogenic differentiation of umbilical cord mesenchymal stem cells by associated with YTHDF2 in a m6A‐miRNA interaction manner Haoqing Yang Wanqing Wang Huina Liu Chen Zhang Yangyang Cao Lujue Long Xiao Han Yuejun Wang Fei Yan Guoqing Li Mengyuan Zhu Luyuan Jin Zhipeng Fan Cell Proliferation AbstractTo investigate the role and mechanism of FBLN1 in the osteogenic differentiation and bone regeneration by using umbilical cord mesenchymal stem cells (WJCMSCs). We found that FBLN1 promoted osteogenic differentiation of WJCMSCs and WJCMSC‐mediated bone regeneration. It was showed that there was an m6A methylation site in 3′UTR of FBLN1 mRNA, and the mutation of the m6A site enhanced the stability of FBLN1 mRNA, subsequently fostering the FBLN1 enhanced osteogenic differentiation of WJCMSCs. YTHDF2 was identified as capable of recognizing and binding to the m6A site, consequently inducing FBLN1 instability and repressed the osteogenic differentiation of WJCMSCs. Meanwhile, miR‐615‐3p negatively regulated FBLN1 by binding FBLN1 3′UTR and inhibited the osteogenic differentiation of WJCMSCs and WJCMSC‐mediated bone regeneration. Then, we discovered miR‐615‐3p was found to regulate the functions of FBLN1 facilitated by YTHDF2 through an m6A‐miRNA regulation mechanism. We demonstrated that FBLN1 is critical for regulating the osteogenic differentiation potentials of WJCMSCs and have identified that miR615‐3p mediated the decay of FBLN1 mRNA which facilitated by m6A reading protein YTHDF2. This provided a novel m6A‐miRNA epigenetic regulatory pattern for MSC regulation and bone regeneration. 10.1111/cpr.13607 http://creativecommons.org/licenses/by/4.0/ |
| doi_str_mv | 10.1111/cpr.13607 |
| format | Artículo Open Access |
| id | wiley_oa_10_1111_cpr_13607 |
| institution | Wiley Open Access |
| license_str_mv | http://creativecommons.org/licenses/by/4.0/ |
| publishDate | 2024 |
| publisher | Wiley |
| record_format | wiley_oa |
| spellingShingle | miR615‐3p inhibited FBLN1 and osteogenic differentiation of umbilical cord mesenchymal stem cells by associated with YTHDF2 in a m6A‐miRNA interaction manner Haoqing Yang Wanqing Wang Huina Liu Chen Zhang Yangyang Cao Lujue Long Xiao Han Yuejun Wang Fei Yan Guoqing Li Mengyuan Zhu Luyuan Jin Zhipeng Fan Cell Proliferation miR615‐3p inhibited FBLN1 and osteogenic differentiation of umbilical cord mesenchymal stem cells by associated with YTHDF2 in a m6A‐miRNA interaction manner Haoqing Yang Wanqing Wang Huina Liu Chen Zhang Yangyang Cao Lujue Long Xiao Han Yuejun Wang Fei Yan Guoqing Li Mengyuan Zhu Luyuan Jin Zhipeng Fan Cell Proliferation AbstractTo investigate the role and mechanism of FBLN1 in the osteogenic differentiation and bone regeneration by using umbilical cord mesenchymal stem cells (WJCMSCs). We found that FBLN1 promoted osteogenic differentiation of WJCMSCs and WJCMSC‐mediated bone regeneration. It was showed that there was an m6A methylation site in 3′UTR of FBLN1 mRNA, and the mutation of the m6A site enhanced the stability of FBLN1 mRNA, subsequently fostering the FBLN1 enhanced osteogenic differentiation of WJCMSCs. YTHDF2 was identified as capable of recognizing and binding to the m6A site, consequently inducing FBLN1 instability and repressed the osteogenic differentiation of WJCMSCs. Meanwhile, miR‐615‐3p negatively regulated FBLN1 by binding FBLN1 3′UTR and inhibited the osteogenic differentiation of WJCMSCs and WJCMSC‐mediated bone regeneration. Then, we discovered miR‐615‐3p was found to regulate the functions of FBLN1 facilitated by YTHDF2 through an m6A‐miRNA regulation mechanism. We demonstrated that FBLN1 is critical for regulating the osteogenic differentiation potentials of WJCMSCs and have identified that miR615‐3p mediated the decay of FBLN1 mRNA which facilitated by m6A reading protein YTHDF2. This provided a novel m6A‐miRNA epigenetic regulatory pattern for MSC regulation and bone regeneration. 10.1111/cpr.13607 http://creativecommons.org/licenses/by/4.0/ |
| title | miR615‐3p inhibited FBLN1 and osteogenic differentiation of umbilical cord mesenchymal stem cells by associated with YTHDF2 in a m6A‐miRNA interaction manner |
| topic | Cell Proliferation |
| url | https://onlinelibrary.wiley.com/doi/10.1111/cpr.13607 |