Shin Rita Lih-Ying, Lee Chien-Wei, Shen Oscar Yuan-Jie, Xu Hongtao, Lee Oscar Kuang-Sheng
Department of Orthopaedics and Traumatology, Faculty of Medicine, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.
Institute for Tissue Engineering and Regenerative Medicine, The Chinese University of Hong Kong, Hong Kong SAR 999077, China.
Stem Cells Int. 2021 Jun 14;2021:8835156. doi: 10.1155/2021/8835156. eCollection 2021.
Bone regeneration is a complex and well-coordinated process that involves crosstalk between immune cells and resident cells in the injury site. Transplantation of mesenchymal stem cells (MSCs) is a promising strategy to enhance bone regeneration. Growing evidence suggests that macrophages have a significant impact on osteogenesis during bone regeneration. However, the precise mechanisms by which macrophage subtypes influence bone regeneration and how MSCs communicate with macrophages have not yet been fully elucidated. In this systematic literature review, we gathered evidence regarding the crosstalk between MSCs and macrophages during bone regeneration. According to the PRISMA protocol, we extracted literature from PubMed and Embase databases by using "mesenchymal stem cells" and "macrophages" and "bone regeneration" as keywords. Thirty-three studies were selected for this review. MSCs isolated from both bone marrow and adipose tissue and both primary macrophages and macrophage cell lines were used in the selected studies. In conclusion, anti-inflammatory macrophages (M2) have significantly more potential to strengthen bone regeneration compared with naïve (M0) and classically activated macrophages (M1). Transplantation of MSCs induced M1-to-M2 transition and transformed the skeletal microenvironment to facilitate bone regeneration in bone fracture and bone defect models. This review highlights the complexity between MSCs and macrophages, providing more insight into the polarized macrophage behavior in this evolving field of osteoimmunology. The results may serve as a useful reference for definite success in MSC-based therapy based on the critical interaction with macrophages.
骨再生是一个复杂且协调良好的过程,涉及免疫细胞与损伤部位的驻留细胞之间的相互作用。间充质干细胞(MSC)移植是促进骨再生的一种有前景的策略。越来越多的证据表明,巨噬细胞在骨再生过程中对骨生成有显著影响。然而,巨噬细胞亚型影响骨再生的精确机制以及MSC与巨噬细胞如何相互作用尚未完全阐明。在这项系统的文献综述中,我们收集了有关骨再生过程中MSC与巨噬细胞相互作用的证据。根据PRISMA方案,我们以“间充质干细胞”、“巨噬细胞”和“骨再生”为关键词,从PubMed和Embase数据库中提取文献。本综述共选取了33项研究。所选研究中使用了从骨髓和脂肪组织分离的MSC以及原代巨噬细胞和巨噬细胞系。总之,与未激活的(M0)和经典激活的巨噬细胞(M1)相比,抗炎巨噬细胞(M2)在增强骨再生方面具有更大的潜力。MSC移植诱导M1向M2转变,并改变骨骼微环境,以促进骨折和骨缺损模型中的骨再生。本综述强调了MSC与巨噬细胞之间的复杂性,为这个不断发展的骨免疫学领域中极化的巨噬细胞行为提供了更多见解。这些结果可能为基于与巨噬细胞关键相互作用的基于MSC的治疗取得明确成功提供有用的参考。