Takabatake Kiyofumi, Tsujigiwa Hidetsugu, Nakano Keisuke, Chang Anqi, Piao Tianyan, Inada Yasunori, Arashima Takuma, Morimatsu Ayumi, Tanaka Ayumi, Kawai Hotaka, Nagatsuka Hitoshi
Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama 700-8525, Japan.
Department of Life Science, Faculty of Science, Okayama University of Science, Okayama 700-0005, Japan.
Materials (Basel). 2024 Aug 19;17(16):4108. doi: 10.3390/ma17164108.
The polarization balance of M1/M2 macrophages with different functions is important in osteogenesis and bone repair processes. In a previous study, we succeeded in developing honeycomb tricalcium phosphate (TCP), which is a cylindrical scaffold with a honeycomb arrangement of straight pores, and we demonstrated that TCP with 300 and 500 μm pore diameters (300TCP and 500TCP) induced bone formation within the pores. However, the details of the influence of macrophage polarization on bone formation using engineered biomaterials, especially with respect to the geometric structure of the artificial biomaterials, are unknown. In this study, we examined whether differences in bone tissue formation due to differences in TCP geometry were due to the polarity of the assembling macrophages. Immunohistochemistry for IBA-1, iNOS, and CD163 single staining was performed. The 300TCP showed a marked infiltration of iNOS-positive cells, which are thought to be M1 macrophages, during the osteogenesis process, while no involvement of CD163-positive cells, which are thought to be M2 macrophages, was observed in the TCP pores. In addition, 500TCP showed a clustering of iNOS-positive cells and CD163-positive cells at 2 weeks, suggesting the involvement of M2 macrophages in the formation of bone tissue in the TCP pores. In conclusion, we demonstrated for the first time that the geometrical structure of the artificial biomaterial, i.e., the pore size of honeycomb TCP, affects the polarization of M1/2 macrophages and bone tissue formation in TCP pores.
具有不同功能的M1/M2巨噬细胞的极化平衡在骨生成和骨修复过程中至关重要。在先前的一项研究中,我们成功开发出了蜂窝状磷酸三钙(TCP),它是一种具有直孔蜂窝状排列的圆柱形支架,并且我们证明了孔径为300和500μm的TCP(300TCP和500TCP)能在孔内诱导骨形成。然而,使用工程生物材料时巨噬细胞极化对骨形成的影响细节,尤其是关于人工生物材料的几何结构方面,尚不清楚。在本研究中,我们研究了由于TCP几何结构差异导致的骨组织形成差异是否归因于聚集巨噬细胞的极性。进行了IBA-1、诱导型一氧化氮合酶(iNOS)和CD163单染色的免疫组织化学检测。在骨生成过程中,300TCP显示出iNOS阳性细胞(被认为是M1巨噬细胞)的显著浸润,而在TCP孔中未观察到CD163阳性细胞(被认为是M2巨噬细胞)的参与。此外,500TCP在2周时显示出iNOS阳性细胞和CD163阳性细胞的聚集,表明M2巨噬细胞参与了TCP孔内骨组织的形成。总之,我们首次证明了人工生物材料的几何结构,即蜂窝状TCP的孔径,会影响M1/2巨噬细胞的极化以及TCP孔内的骨组织形成。