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FN 涂层物理梯度水凝胶上的巨噬细胞表型变化。

Macrophage Phenotypic Changes on FN-Coated Physical Gradient Hydrogels.

机构信息

Department of Materials Science & Engineering, Iowa State University, Ames, Iowa 50011, United States.

Department of Chemical & Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.

出版信息

ACS Appl Bio Mater. 2021 Sep 20;4(9):6758-6768. doi: 10.1021/acsabm.1c00489. Epub 2021 Aug 25.

DOI:10.1021/acsabm.1c00489
PMID:35006977
Abstract

The chemical and physical properties are two crucial cues when designing tissue engineering scaffold to mimic living tissue. Macrophages, the major players in the immune response, react rapidly to microenvironmental signals, including gradients of physical or chemical cues. Spatiotemporal gradients can modulate cell behavior, such as polarization, proliferation, and adhesion. Here, we studied macrophage phenotypic changes on untreated and fibronectin (FN)-coated methacrylated gellan gum with varying stiffnesses. The compressive moduli of hydrogel with different stiffnesses ranged from ∼5 to 30 kPa. Fibronectin was chemically attached to the substrate to facilitate macrophage proliferation, adhesion, and polarization. Classically (M1) and alternatively (M2) activated macrophages were cultured on both untreated and FN-coated gels. FN-coated substrates elevated cell numbers and enhanced macrophage spreading. The urea/nitrite ratio indicated that untreated rigid substrates shifted both polarizations toward a more proinflammatory phenotype. FN-coated substrates had no impact on M1 polarization. In contrast, FN-coated stiffer gels polarized M2 cells toward an anti-proinflammatory state based on arginine activity and CD206 expression. In addition, macrophage polarization on the softer gel was not influenced by the neighboring cells cultured on the stiffer side of the gel. Using mechanical gradients to control macrophage polarization can be a useful tool in ensuring a proper healing response and for tissue engineering.

摘要

在设计模仿活体组织的组织工程支架时,化学和物理性质是两个关键线索。巨噬细胞是免疫反应的主要参与者,它们会迅速对微环境信号做出反应,包括物理或化学线索的梯度变化。时空梯度可以调节细胞行为,如极化、增殖和黏附。在这里,我们研究了未经处理和纤维连接蛋白 (FN) 涂层的甲基丙烯酰化凝胶多糖在不同硬度下对巨噬细胞表型变化的影响。不同硬度水凝胶的压缩模量范围从约 5 到 30 kPa。纤维连接蛋白通过化学附着到基底上,以促进巨噬细胞的增殖、黏附和极化。经典激活 (M1) 和替代激活 (M2) 的巨噬细胞分别在未经处理和 FN 涂层凝胶上培养。FN 涂层基底增加了细胞数量并增强了巨噬细胞的铺展。尿素/亚硝酸盐比值表明,未经处理的刚性基底使两种极化都向更具炎症表型的方向转变。FN 涂层基底对 M1 极化没有影响。相比之下,FN 涂层较硬的凝胶根据精氨酸活性和 CD206 表达将 M2 细胞极化到抗炎状态。此外,较软凝胶上的巨噬细胞极化不受与其相邻的在较硬凝胶一侧培养的细胞的影响。使用机械梯度来控制巨噬细胞极化可以成为确保适当愈合反应和组织工程的有用工具。

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