首页> 外文期刊>Journal of biomedical materials research, Part A >Macrophage reprogramming: Influence of latex beads with various functional groups on macrophage phenotype and phagocytic uptake in vitro
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Macrophage reprogramming: Influence of latex beads with various functional groups on macrophage phenotype and phagocytic uptake in vitro

机译:巨噬细胞重编程:不同功能基团的乳胶珠对体外巨噬细胞表型和吞噬细胞吸收的影响。

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摘要

Macrophages play a crucial role in initiating immune responses with various functions ranging from wound healing to antimicrobial actions. The type of biomaterial is suggested to influence macrophage phenotype. Here, we show that exposing M1- and M2-activated macrophages to polystyrene latex beads bearing different functional groups can alter secretion profiles, providing a possible method for altering the course of the host response. Macrophages were stimulated with either lipopolysaccharide or interleukin (IL) 4 and cultured for 24 h with 10 different latex beads. Proinflammatory cytokines (tumor necrosis factor , monocyte chemotactic protein 1) and nitrite served as markers for the M1 phenotype and proangiogenic cytokine (IL-10) and arginase activity for M2 cells. The ability of the macrophages to phagocytize Escherichia coli particles and water contact angles of the polymers were also assessed. Different patterns of cytokine expression and phagocytosis activity were induced by the various particles. Particles did not polarize the cells toward one specific phenotype versus another, but rather induced changes in both pro- and anti-inflammatory markers. Our results suggest a dependence of pro- and anti-inflammatory cytokines and phagocytic activities on material type and cytokine stimuli. These data also illustrate how biomaterials can be exploited to alter host responses for drug delivery and tissue engineering applications. (c) 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 262-268, 2015.
机译:巨噬细胞在引发免疫反应中起着至关重要的作用,其免疫功能从伤口愈合到抗菌作用不等。建议生物材料的类型影响巨噬细胞表型。在这里,我们表明,将M1和M2活化的巨噬细胞暴露于带有不同官能团的聚苯乙烯胶乳珠可以改变分泌谱,为改变宿主反应的过程提供一种可能的方法。用脂多糖或白介素(IL)4刺激巨噬细胞,并用10个不同的乳胶珠培养24 h。促炎细胞因子(肿瘤坏死因子,单核细胞趋化蛋白1)和亚硝酸盐充当M1表型和促血管生成细胞因子(IL-10)和M2细胞精氨酸酶活性的标记。还评估了巨噬细胞吞噬大肠杆菌颗粒的能力和聚合物的水接触角。各种颗粒诱导了不同类型的细胞因子表达和吞噬活性。颗粒并未使细胞相对于另一种特定的表型极化,而是诱导了促炎和抗炎标志物的变化。我们的结果表明促炎和抗炎细胞因子以及吞噬活性对物质类型和细胞因子刺激的依赖性。这些数据还说明了如何利用生物材料来改变宿主对药物递送和组织工程应用的反应。 (c)2014 Wiley Periodicals,Inc. J Biomed Mater Res Part A:103A:262-268,2015年。

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