Xu Daorong, Qian Jikun, Guan Xin, Ren Ling, Yang Kaifan, Huang Xuan, Zhang Shuyuan, Chai Yu, Wu Xiaohu, Wu Hangtian, Zhang Xianrong, Yang Ke, Yu Bin
Division of Orthopedic Surgery, Department of Orthopedics, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Guangdong Provincial Key Laboratory of Bone and Cartilage Regenerative Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Front Bioeng Biotechnol. 2021 Jan 14;8:620629. doi: 10.3389/fbioe.2020.620629. eCollection 2020.
In the mammalian skeletal system, osteogenesis and angiogenesis are closely linked by type H vessels during bone regeneration and repair. Our previous studies confirmed the promotion of these processes by copper-containing metal (CCM) and . However, whether and how the coupling of angiogenesis and osteogenesis participates in the promotion of bone regeneration by CCM is unknown. In this study, M2a macrophages but not M2c macrophages were shown to be immunoregulated by CCM. A CCM, 316L-5Cu, was applied to drilling hole injuries of the tibia of C57/6 mice for comparison. We observed advanced formation of cortical bone and type H vessels beneath the new bone in the 316L-5Cu group 14 and 21 days postinjury. Moreover, the recruitment of CD206-positive M2a macrophages, which are regarded as the primary source of platelet-derived growth factor type BB (PDGF-BB), was significantly promoted at the injury site at days 14 and 21. Under the stimulation of CCM, mitochondria-derived reactive oxygen species were also found to be upregulated in CD206 M2a macrophages , and this upregulation was correlated with the expression of PDGF-BB. In conclusion, our results indicate that CCM promotes the evolution of callus through the generation of type H vessels during the process of bone repair by upregulating the expression of PDGF-BB derived from M2a macrophages.
在哺乳动物骨骼系统中,在骨再生和修复过程中,H型血管将骨生成与血管生成紧密联系在一起。我们之前的研究证实了含铜金属(CCM)对这些过程的促进作用。然而,血管生成与骨生成的耦合是否以及如何参与CCM对骨再生的促进作用尚不清楚。在本研究中,显示M2a巨噬细胞而非M2c巨噬细胞受到CCM的免疫调节。将一种CCM,即316L-5Cu,应用于C57/6小鼠胫骨的钻孔损伤处进行比较。我们观察到,在损伤后14天和21天,316L-5Cu组新骨下方的皮质骨和H型血管形成提前。此外,在损伤后第14天和第21天,损伤部位CD206阳性M2a巨噬细胞(被认为是血小板衍生生长因子BB型(PDGF-BB)的主要来源)的募集显著增加。在CCM的刺激下,还发现CD206 M2a巨噬细胞中线粒体衍生的活性氧上调,且这种上调与PDGF-BB的表达相关。总之,我们的结果表明,CCM在骨修复过程中通过上调源自M2a巨噬细胞的PDGF-BB的表达,通过生成H型血管促进骨痂的演变。