Zhang Dingmei, Dang Yi, Deng Renli, Ma Yaping, Wang Jing, Ao Jun, Wang Xin
Department of Orthopaedic Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou 563003, China.
Nurse Department, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou 563003, China.
J Tissue Eng Regen Med. 2023 Feb 7;2023:1512966. doi: 10.1155/2023/1512966. eCollection 2023.
Bone tissue regeneration plays an increasingly important role in contemporary clinical treatment. The reconstruction of bone defects remains a huge challenge for clinicians. Bone regeneration is regulated by the immune system, in which inflammation is an important regulating factor in bone formation and remodeling. As the main cells involved in inflammation, macrophages play a key role in osteogenesis by polarizing into different phenotypes during different stages of bone regeneration. Considering this, this review mainly summarizes the function of macrophage in bone regeneration based on mesenchymal stem cells (MSCs), osteoblasts, osteoclasts, and vascular cells. In conclusion, anti-inflammatory macrophages (M2) have a greater potentiality to promote bone regeneration than M0 and classically activated proinflammatory macrophages (M1). In the fracture and bone defect models, tissue engineering materials can induce the transition from M1 to M2, alter the bone microenvironment, and promote bone regeneration through interactions with bone-related cells and blood vessels. The review provides a further understanding of macrophage polarization behavior in the evolving field of bone immunology.
骨组织再生在当代临床治疗中发挥着越来越重要的作用。骨缺损的修复对临床医生来说仍然是一个巨大的挑战。骨再生受免疫系统调节,其中炎症是骨形成和重塑的重要调节因子。巨噬细胞作为参与炎症的主要细胞,在骨再生的不同阶段通过极化为不同表型在成骨过程中发挥关键作用。基于此,本综述主要基于间充质干细胞(MSCs)、成骨细胞、破骨细胞和血管细胞总结巨噬细胞在骨再生中的作用。总之,抗炎巨噬细胞(M2)比M0和经典活化的促炎巨噬细胞(M1)具有更大的促进骨再生的潜力。在骨折和骨缺损模型中,组织工程材料可诱导M1向M2转变,改变骨微环境,并通过与骨相关细胞和血管的相互作用促进骨再生。本综述进一步加深了对骨免疫学不断发展领域中巨噬细胞极化行为的理解。