锶通过不对称细胞分裂调控成骨分化过程中的干细胞命运

Yanqun Li, Jianhui Yue, Yuan Liu, Jun Wu, Min Guan, Di Chen, H. Pan, Zhao, W. Lu
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引用次数: 0

摘要

锶作为一种流行的成骨成分已被纳入各种类型的骨科生物材料,以提高骨再生。它具有促进骨形成和抑制骨吸收的双重作用。研究集中在锶在调节干细胞行为以启动再生能力方面的作用。然而,锶调控干细胞命运和体内平衡的机制尚未完全阐明。本研究通过体外和体内实验证实了锶对间充质干细胞成骨分化的促进作用。有趣的是,在对锶处理的反应中,干细胞进行不对称细胞分裂以平衡干细胞维持和成骨分化。子干细胞中Par复合物的不对称分布通过选择性激活成骨转录因子诱导不同的细胞命运。锶激活非规范Wnt信号调节Par复合物分布。了解锶调控干细胞命运的机制可以促进生物材料设计以启动内源性骨再生能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Strontium Regulates Stem Cells Fates During Osteogenic Differentiation Through an Asymmetric Cell Division
Strontium as a popular osteogenic component has been incorporated into various types of orthopaedic biomaterials to enhance bone regeneration. It performs dual effects in promoting bone formation and inhibiting bone resorption. Studies have focused on the effects of strontium in regulating stem cells behaviors to initiate regenerative capacity. However, the mechanism of strontium on regulating stem cells fates and homeostasis has not been fully elucidated. In this study, the promoted effect of strontium on osteogenic differentiation of mesenchymal stem cells was confirmed both in vitro and in vivo. Interestingly, in responding to strontium treatment, stem cells performed asymmetric cell division to balance stemness maintenance and osteogenic differentiation. Asymmetric distribution of Par complex in daughter stem cells induced different cell fates by discriminately activating of osteogenic transcription factors. Strontium activated noncanonical Wnt signaling to regulate Par complex distribution. Understanding the mechanism of strontium on regulating stem cell fate could facilitate biomaterials designing to initiate endogenous bone regenerative capacity.
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