State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, No. 14, Section 3, Ren Min Nan Rd, Chengdu, 610041, Sichuan, China.
School of Engineering and Materials Science, Queen Mary University of London, UK.
J Mater Chem B. 2020 Mar 4;8(9):1863-1877. doi: 10.1039/c9tb02932j.
To investigate the roles of macrophages in material-instructed bone formation, two calcium phosphate (TCP) ceramics with the same chemistry but various scales of surface topography were employed in this study. After being implanted subcutaneously in FVB mice for 8 weeks, TCPs (TCP ceramics with submicron surface topography) gave rise to bone formation, while TCPb (TCP ceramics with micron surface topography) did not, showing the crucial role of surface topography scale in material-instructed bone formation. Depletion of macrophages with liposomal clodronate (LipClod) blocked such bone formation instructed by TCPs, confirming the role of macrophages in material-instructed bone formation. Macrophage cells (i.e. RAW 264.7 cells) cultured on TCPs in vitro polarized to tissue repair macrophages as evidenced by gene expression and cytokine production, while polarizing to pro-inflammatory macrophages on TCPb. Submicron surface topography of TCP ceramics directed macrophage polarization via PI3K/AKT pathways with the synergistic regulation of integrin β1. Finally, the tissue repair macrophage polarization on TCPs resulted in osteogenic differentiation of mesenchymal stem cells in vitro. At early implantation in FVB mice, TCPs recruited more macrophages which polarized towards tissue repair macrophages with time. The present data demonstrate the important roles of macrophage polarization in bone formation instructed by calcium phosphate ceramics.
为了研究巨噬细胞在材料诱导骨形成中的作用,本研究采用了两种具有相同化学组成但表面形貌尺度不同的磷酸钙(TCP)陶瓷。将 TCP 陶瓷(具有亚微米表面形貌)和 TCPb(具有微米表面形貌)分别植入 FVB 小鼠皮下 8 周后,TCP 陶瓷诱导了骨形成,而 TCPb 则没有,这表明表面形貌尺度在材料诱导骨形成中起着关键作用。用脂质体氯膦酸(LipClod)耗竭巨噬细胞可阻止 TCP 诱导的这种骨形成,证实了巨噬细胞在材料诱导骨形成中的作用。体外培养在 TCP 陶瓷上的巨噬细胞(即 RAW264.7 细胞)向组织修复型巨噬细胞极化,这可通过基因表达和细胞因子产生来证实,而在 TCPb 上则向促炎型巨噬细胞极化。TCP 陶瓷的亚微米表面形貌通过 PI3K/AKT 途径指导巨噬细胞极化,整合素 β1 起协同调节作用。最后,TCP 上的组织修复型巨噬细胞极化导致间充质干细胞的成骨分化。在 FVB 小鼠早期植入时,TCP 招募了更多的巨噬细胞,这些巨噬细胞随着时间的推移向组织修复型巨噬细胞极化。这些数据表明巨噬细胞极化在磷酸钙陶瓷诱导的骨形成中起着重要作用。