Macrophage responses to selective laser‐melted Ti‐6Al‐4V scaffolds of different pore geometries and the corresponding osteoimmunomodulatory effects toward osteogenesis

材料科学 脚手架 巨噬细胞极化 巨噬细胞 选择性激光熔化 免疫系统 六方晶系 生物物理学 生物医学工程 复合材料 体外 免疫学 化学 微观结构 生物 结晶学 生物化学 医学
作者
Yunqi Wu,Zheng Liu,Zhenchao Xu,Yilu Zhang,Hongru Ye,Xiyang Wang
出处
期刊:Journal of Biomedical Materials Research Part A [Wiley]
卷期号:110 (4): 873-883 被引量:5
标识
DOI:10.1002/jbm.a.37335
摘要

Following recent advances in osteoimmunology, there is growing recognition of the vital role of immune cells in the osteogenesis process. The 3D-printed scaffold, as a substitute for injured and/or diseased bone tissues, has demonstrated satisfactory pro-osteogenetic performance. However, whether immune cells prompt the above pro-osteogenetic performance has not been elucidated in detail. In the present study, highly controllable Ti-6Al-4V scaffolds with different pore geometries were fabricated using a selective laser-melting technique, to reveal their osteoimmunological functions with macrophages. The results showed that macrophages displayed characteristics of M2 phenotype in response to scaffolds. As a result, an anti-inflammatory microenvironment was generated. When the pore geometry was considered, such observations were more apparent with the hexagonal pore scaffold than with the triangular one. In addition, inhibition of the toll-like receptor signaling pathway in macrophages has been proposed to cause the above phenomenon. Upon applying conditioned media derived from macrophages on pre-osteoblasts, the hexagonal pore scaffold group was found to significantly enhance osteoblastic differentiation, via macrophage-to-implant interactions. However, the effect of triangular pore scaffold was not statistically significant compared to that of hexagonal pore scaffolds or nonporous samples. In an attempt to quantify scaffold pore geometries, it was suggested that pores with higher circularity values tended to induce M2 polarization of macrophages, promote an anti-inflammatory milieu, and therefore, achieve better osteogenetic performance via immunomodulation.
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