《口腔颌面外科杂志》 ›› 2016, Vol. 26 ›› Issue (6): 441-. doi: 10.3969/j.issn.1005-4979.2016.06.014

• 综述 • 上一篇    下一篇

间充质干细胞调控破骨细胞分化及功能的研究进展

许舒宇(综述),王佐林(审校)   

  1. 同济大学口腔医学院·同济大学附属口腔医院种植科,上海牙组织修复与再生工程技术研究中心
  • 收稿日期:2016-05-11 修回日期:2016-05-15 出版日期:2016-12-28 发布日期:2017-06-30
  • 通讯作者: 王佐林,教授. E-mail: zuolin@ tongji.edu.cn E-mail:zuolin@ tongji.edu.cn
  • 作者简介:许舒宇(1988—),女,山东人,博士研究生. E-mail: Hillary_xu@hotmail.com
  • 基金资助:

    国家科技支撑计划项目(2014BAI04B07);国家自然科学基金面上项目(81271110);中央高校基本科研业务费专项资金项目(20152957)

Recent Advances in the Effects of Mesenchymal Stem Cells on Osteoclastogenesis

XU Shu-yu, WANG Zuo-lin   

  1. Department of Implantology, School and Hospital of Stomatology, Tongji University, Shanghai Engineering Research Center of Tooth Restoration and Regeneration
  • Received:2016-05-11 Revised:2016-05-15 Online:2016-12-28 Published:2017-06-30

摘要: 间充质干细胞(MSCs)对骨代谢的作用是多方面的。MSCs对破骨细胞和骨吸收的调控是其中一个很重要的方面。MSCs对破骨有双面的调节作用,可能促进或者抑制,取决于炎症环境的情况。在一些生理、病理环境下,MSCs通过分泌相关细胞因子对破骨细胞的形成及功能起正向调控作用。但在某些炎症状态下,MSCs可能也通过旁分泌作用实现对破骨细胞形成和分化的抑制作用,尤其是在体外共培养破骨细胞与MSCs,MSCs对破骨细胞的形成表现出抑制作用。了解MSCs对破骨细胞的调控作用,有助于了解炎症微环境下MSCs对骨丢失的治疗潜能。

关键词: 间充质干细胞, 破骨, 旁分泌

Abstract: The effect of mesenchymal stem cells (MSCs) on bone formation is complex and various. The effect of MSCs on osteoclastogenesis and bone resorption is a main aspect. Bone resorption is tightly and dynamically regulated by multiple mediators, including cytokines that act directly on osteoclasts and their precursors, or indirectly by modulating osteoblast lineage cells that in turn regulate osteoclast differentiation. Under some physiological conditions, the cytokines produced by MSCs have important roles in a diverse range of osteoclastogenesis processes. However, during inflammation, MSCs suppress osteoclast formation and activity, partly via paracrine effects. MSCs thus seem to have a dual effect, by stimulating or inhibiting osteoclastogenesis, depending on the inflammatory level. This effect of MSCs on osteoclast formation may be exploited for the therapeutic potential of MSCs in bone loss associated with inflammatory diseases.

Key words:  mesenchymal stem cells, osteoclastogenic, paracrine

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