miR-203-3p 通过下调 Pbk 促进小鼠骨髓间充质干细胞的衰老。

IF 7.8 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology
Aging Cell Pub Date : 2024-08-09 DOI:10.1111/acel.14293
Qiaojuan Mei, Kexin Li, Tianyu Tang, Siying Cai, Yu Liu, Xiaofei Wang, Yinzhao Jia, Ling Zhang, Huaibiao Li, Hui Song, Jun Zhai, Wenpei Xiang
{"title":"miR-203-3p 通过下调 Pbk 促进小鼠骨髓间充质干细胞的衰老。","authors":"Qiaojuan Mei,&nbsp;Kexin Li,&nbsp;Tianyu Tang,&nbsp;Siying Cai,&nbsp;Yu Liu,&nbsp;Xiaofei Wang,&nbsp;Yinzhao Jia,&nbsp;Ling Zhang,&nbsp;Huaibiao Li,&nbsp;Hui Song,&nbsp;Jun Zhai,&nbsp;Wenpei Xiang","doi":"10.1111/acel.14293","DOIUrl":null,"url":null,"abstract":"<p>The senescence of bone marrow mesenchymal stem cells (BMSCs) contributes to the development of degenerative skeletal conditions. To date, the molecular mechanism resulting in BMSC senescence has not been fully understood. In this study, we identified a small non-coding RNA, miR-203-3p, the expression of which was elevated in BMSCs from aged mice. On the other hand, overexpression of miR-203-3p in BMSCs from young mice reduced cell growth and enhanced their senescence. Mechanistically, PDZ-linked kinase (PBK) is predicted to be the target of miR-203-3p. The binding of miR-203-3p to Pbk mRNA could decrease its expression, which in turn inhibited the ubiquitination-mediated degradation of p53. Furthermore, the intravitreal injection of miR-203-3p-inhibitor into the bone marrow cavity of aged mice attenuated BMSC senescence and osteoporosis in aged mice. Collectively, these findings suggest that targeting miR-203-3p to delay BMSC senescence could be a potential therapeutic strategy to alleviate age-related osteoporosis.</p>","PeriodicalId":55543,"journal":{"name":"Aging Cell","volume":"23 11","pages":""},"PeriodicalIF":7.8000,"publicationDate":"2024-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11561657/pdf/","citationCount":"0","resultStr":"{\"title\":\"miR-203-3p promotes senescence of mouse bone marrow mesenchymal stem cells via downregulation of Pbk\",\"authors\":\"Qiaojuan Mei,&nbsp;Kexin Li,&nbsp;Tianyu Tang,&nbsp;Siying Cai,&nbsp;Yu Liu,&nbsp;Xiaofei Wang,&nbsp;Yinzhao Jia,&nbsp;Ling Zhang,&nbsp;Huaibiao Li,&nbsp;Hui Song,&nbsp;Jun Zhai,&nbsp;Wenpei Xiang\",\"doi\":\"10.1111/acel.14293\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The senescence of bone marrow mesenchymal stem cells (BMSCs) contributes to the development of degenerative skeletal conditions. To date, the molecular mechanism resulting in BMSC senescence has not been fully understood. In this study, we identified a small non-coding RNA, miR-203-3p, the expression of which was elevated in BMSCs from aged mice. On the other hand, overexpression of miR-203-3p in BMSCs from young mice reduced cell growth and enhanced their senescence. Mechanistically, PDZ-linked kinase (PBK) is predicted to be the target of miR-203-3p. The binding of miR-203-3p to Pbk mRNA could decrease its expression, which in turn inhibited the ubiquitination-mediated degradation of p53. Furthermore, the intravitreal injection of miR-203-3p-inhibitor into the bone marrow cavity of aged mice attenuated BMSC senescence and osteoporosis in aged mice. Collectively, these findings suggest that targeting miR-203-3p to delay BMSC senescence could be a potential therapeutic strategy to alleviate age-related osteoporosis.</p>\",\"PeriodicalId\":55543,\"journal\":{\"name\":\"Aging Cell\",\"volume\":\"23 11\",\"pages\":\"\"},\"PeriodicalIF\":7.8000,\"publicationDate\":\"2024-08-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11561657/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Aging Cell\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/acel.14293\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Biochemistry, Genetics and Molecular Biology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aging Cell","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/acel.14293","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0

摘要

骨髓间充质干细胞(BMSCs)的衰老是导致骨骼退行性病变的原因之一。迄今为止,导致骨髓间充质干细胞衰老的分子机制尚未完全明了。在这项研究中,我们发现了一种小的非编码 RNA miR-203-3p,它在衰老小鼠的 BMSCs 中表达升高。另一方面,在年轻小鼠的 BMSCs 中过表达 miR-203-3p 会降低细胞的生长并增强其衰老。从机理上预测,PDZ 链接激酶(PBK)是 miR-203-3p 的靶标。miR-203-3p 与 Pbk mRNA 结合可降低其表达,进而抑制泛素化介导的 p53 降解。此外,向老龄小鼠骨髓腔静脉注射 miR-203-3p 抑制剂可减轻老龄小鼠 BMSC 的衰老和骨质疏松症。总之,这些研究结果表明,以miR-203-3p为靶点延缓BMSC衰老可能是缓解与年龄相关的骨质疏松症的一种潜在治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

miR-203-3p promotes senescence of mouse bone marrow mesenchymal stem cells via downregulation of Pbk

miR-203-3p promotes senescence of mouse bone marrow mesenchymal stem cells via downregulation of Pbk

miR-203-3p promotes senescence of mouse bone marrow mesenchymal stem cells via downregulation of Pbk

The senescence of bone marrow mesenchymal stem cells (BMSCs) contributes to the development of degenerative skeletal conditions. To date, the molecular mechanism resulting in BMSC senescence has not been fully understood. In this study, we identified a small non-coding RNA, miR-203-3p, the expression of which was elevated in BMSCs from aged mice. On the other hand, overexpression of miR-203-3p in BMSCs from young mice reduced cell growth and enhanced their senescence. Mechanistically, PDZ-linked kinase (PBK) is predicted to be the target of miR-203-3p. The binding of miR-203-3p to Pbk mRNA could decrease its expression, which in turn inhibited the ubiquitination-mediated degradation of p53. Furthermore, the intravitreal injection of miR-203-3p-inhibitor into the bone marrow cavity of aged mice attenuated BMSC senescence and osteoporosis in aged mice. Collectively, these findings suggest that targeting miR-203-3p to delay BMSC senescence could be a potential therapeutic strategy to alleviate age-related osteoporosis.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Aging Cell
Aging Cell 生物-老年医学
CiteScore
14.40
自引率
2.60%
发文量
212
审稿时长
8 weeks
期刊介绍: Aging Cell, an Open Access journal, delves into fundamental aspects of aging biology. It comprehensively explores geroscience, emphasizing research on the mechanisms underlying the aging process and the connections between aging and age-related diseases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信