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3D printed submicron patterns orchestrate the response of macrophages

机译:3 d打印亚微米模式编排巨噬细胞的反应

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摘要

The surface topography of engineered extracellular matrices is one of the most important physical cues regulating the phenotypic polarization of macrophages. However, not much is known about the ways through which submicron (i.e., 100-1000 nm) topographies modulate the polarization of macrophages. In the context of bone tissue regeneration, it is well established that this range of topographies stimulates the osteogenic differentiation of stem cells. Since the immune response affects the bone tissue regeneration process, the immunomodulatory consequences of submicron patterns should be studied prior to their clinical application. Here, we 3D printed submicron pillars (using two-photon polymerization technique) with different heights and interspacings to perform the first ever systematic study of such effects. Among the studied patterns, the highest degree of elongation was observed for the cells cultured on those with the tallest and densest pillars. After 3 days of culture with inflammatory stimuli (LPS/IFN-gamma), sparsely decorated surfaces inhibited the expression of the pro-inflammatory cellular marker CCR7 as compared to day 1 and to the other patterns. Furthermore, sufficiently tall pillars polarized the M1 macrophages towards a pro-healing (M2) phenotype, as suggested by the expression of CD206 within the first 3 days. As some of the studied patterns are known to be osteogenic, the osteoimmunomodulatory capacity of the patterns should be further studied to optimize their bone tissue regeneration performance.
机译:工程细胞外的表面形貌矩阵是最重要的一个物理信号调节的表型分化巨噬细胞。方法通过亚微米(即100 - 1000 nm)地形的偏振调制巨噬细胞。再生,这已是不争范围的地形刺激成骨的干细胞的分化。响应影响骨组织的再生过程中,免疫调节的影响亚微米模式应该学习之前他们的临床应用。亚微米柱(使用双光子与不同高度聚合技术)执行首次和井距系统研究的影响。研究模式,最高程度的伸长细胞培养观察那些拥有最高的和密集的支柱。3天的文化与炎症刺激(有限合伙人/ IFN-gamma),稀疏的表面装饰抑制促炎的表现细胞标记CCR7第一天,相比另一种模式。高大的柱子极化M1巨噬细胞pro-healing (M2)表型,如建议的前3天内CD206的表达。已知的一些研究模式成骨的osteoimmunomodulatory能力应进一步研究模式优化他们的骨组织再生的性能。

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