期刊文献+

补肾中药调控骨髓间充质干细胞成骨分化的RNA m6A修饰作用研究

Effects of Kidney-tonifying Herbs on Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells from the Perspective of m6A Modification
下载PDF
导出
摘要 骨髓间充质干细胞(BMSCs)是一种成体干细胞,具有成骨细胞分化能力。BMSCs成骨分化能力减弱易导致骨质疏松等多种骨相关疾病。中医学认为“肾主骨生髓”,补肾中药是治疗骨质疏松的常用药物,具有调控BMSCs成骨分化作用。腺苷N6位甲基化修饰(m6A)是真核生物RNA的转录后修饰,是BMSCs成骨分化的关键因素。探讨m6A动态修饰与BMSCs成骨分化的关系,分析补肾中药调控m6A修饰的可能作用及靶点,能够为补肾中药治疗骨质疏松提供新靶点,为中医肾藏象理论的科学阐释提供思路。 Bone marrow mesenchymal stem cells(BMSCs) are adult stem cells with osteogenic differentiation ability.The weakening osteogenic differentiation ability of BMSCs can easily lead to a variety of bone-related diseases,such as osteoporosis.Based on the theory of traditional Chinese medicine that “kidney governs the bone and generates the marrow”,kidney-tonifying herbs are commonly used in the treatment of osteoporosis,which has the effect of regulating osteogenic differentiation of BMSCs.N6-methyladenosine(m6A) is a post-transcriptional modification of eukaryotic RNA and a key factor in osteogenic differentiation of BMSCs.This study explores the relationship between m6A dynamic modification and osteogenic differentiation of BMSCs,and analyzes the possible role and targets of kidney-tonifying herbs in regulating m6A modification,which can provide new targets for kidney-tonifying herbs in the treatment of osteoporosis,and provide ideas for the scientific interpretation of the theory of visceral manifestation of kidney in traditional Chinese medicine.
作者 李沂霖 王花欣 田硕 王洁 董仁超 刘艳秋 LI Yilin;WANG Huaxin;TIAN Shuo;WANG Jie;DONG Renchao;LIU Yanqiu(College of Traditional Chinese Medicine,Shandong University of Traditional Chinese Medicine,Ji′nan 250355,China)
出处 《世界中医药》 CAS 北大核心 2024年第2期261-266,共6页 World Chinese Medicine
基金 国家自然科学基金项目(82074134)——二至丸通过Mettl3/14介导m6A动态修饰调控骨髓间充质干细胞成骨分化抗骨质疏松的表观机制。
关键词 骨间充质干细胞 N6甲基腺苷修饰 补肾中药 成骨分化 骨质疏松 靶点 作用机制 肾藏象 Bone marrow mesenchymal stem cells m6A modification Kidney-tonifying herbs Osteogenic differentiation Osteoporosis Target Mechanism Visceral manifestation of kidney
  • 相关文献

参考文献32

二级参考文献254

共引文献364

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部