间充质干细胞
细胞生物学
旁分泌信号
骨愈合
肿瘤抑制因子
干细胞
巨噬细胞
生物
免疫学
再生(生物学)
串扰
炎症
解剖
白细胞介素6
光学
物理
受体
体外
生物化学
作者
Jukka Pajarinen,Tzuhua Lin,Emmanuel Gibon,Yusuke Kohno,Masahiro Maruyama,Karthik Nathan,Laura Lu,Zhenyu Yao,Stuart B. Goodman
出处
期刊:Biomaterials
[Elsevier]
日期:2018-01-02
卷期号:196: 80-89
被引量:659
标识
DOI:10.1016/j.biomaterials.2017.12.025
摘要
Recent research has brought about a clear understanding that successful fracture healing is based on carefully coordinated cross-talk between inflammatory and bone forming cells. In particular, the key role that macrophages play in the recruitment and regulation of the differentiation of mesenchymal stem cells (MSCs) during bone regeneration has been brought to focus. Indeed, animal studies have comprehensively demonstrated that fractures do not heal without the direct involvement of macrophages. Yet the exact mechanisms by which macrophages contribute to bone regeneration remain to be elucidated. Macrophage–derived paracrine signaling molecules such as Oncostatin M, Prostaglandin E2 (PGE2), and Bone Morphogenetic Protein-2 (BMP2) have been shown to play critical roles; however the relative importance of inflammatory (M1) and tissue regenerative (M2) macrophages in guiding MSC differentiation along the osteogenic pathway remains poorly understood. In this review, we summarize the current understanding of the interaction of macrophages and MSCs during bone regeneration, with the emphasis on the role of macrophages in regulating bone formation. The potential implications of aging to this cellular cross-talk are reviewed. Emerging treatment options to improve facture healing by utilizing or targeting MSC-macrophage crosstalk are also discussed.
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