Orthopaedic Research Laboratories, Department of Orthopaedic Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Orthopaedic Research Laboratories, Department of Orthopaedic Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Biomaterials. 2019 Mar;196:80-89. doi: 10.1016/j.biomaterials.2017.12.025. Epub 2018 Jan 2.
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.
最近的研究清楚地表明,成功的骨折愈合是基于炎症细胞和成骨细胞之间精心协调的对话。特别是,巨噬细胞在招募和调节间充质干细胞(MSCs)分化过程中的关键作用在骨再生中受到了关注。事实上,动物研究已经全面证明,没有巨噬细胞的直接参与,骨折就不会愈合。然而,巨噬细胞促进骨再生的确切机制仍有待阐明。巨噬细胞衍生的旁分泌信号分子,如肿瘤坏死因子 M(Oncostatin M)、前列腺素 E2(PGE2)和骨形态发生蛋白 2(BMP2)已被证明发挥着关键作用;然而,炎症(M1)和组织再生(M2)巨噬细胞在指导 MSC 沿着成骨途径分化中的相对重要性仍知之甚少。在这篇综述中,我们总结了目前对巨噬细胞和 MSC 在骨再生过程中的相互作用的理解,重点介绍了巨噬细胞在调节骨形成中的作用。还回顾了衰老对这种细胞对话的潜在影响。讨论了利用或针对 MSC-巨噬细胞相互作用来改善骨折愈合的新兴治疗选择。