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一种用于分析人原代巨噬细胞急性生物材料依赖性反应的培养模型。

A culture model to analyze the acute biomaterial-dependent reaction of human primary macrophages.

机构信息

Department of Otorhinolaryngology, Head and Neck Surgery, Erasmus MC, University Medical Centre Rotterdam, Ee1618, Dr. Molewaterplein 50, 3015 GE Rotterdam, The Netherlands.

出版信息

Biochem Biophys Res Commun. 2013 Mar 29;433(1):115-20. doi: 10.1016/j.bbrc.2013.02.054. Epub 2013 Feb 26.

Abstract

Macrophages are important in foreign body reactions. We devised a culture model with human primary macrophages to evaluate the acute response of macrophages to biomaterials. First we selected proteins representative for pro-inflammatory (M1) or anti-inflammatory/repair (M2) response of monocytes isolated from blood of healthy human donors by exposing them to LPS+IFNγ or IL-4. A relative M1/M2 index was calculated using IL-1β, IL-6, tumor necrosis factor (TNF)α, monocyte chemotactic protein (MCP)-3 and macrophage inflammatory protein (MIP)-1α as M1 markers, and IL-1 receptor antagonist (IL-1RA), CCL18, regulated and normal T-cell expressed and secreted (RANTES), and macrophage-derived chemokine (MDC) as M2 markers. Then monocytes were cultured for 3days on 4 materials selected for known different foreign body reactions: Permacol™, Parietex™ Composite, multifilament polyethylene terephthalate and multifilament polypropylene. Macrophages on polypropylene produced high levels of anti-inflammatory proteins with a low M1/M2 index. Macrophages on Parietex™ Composite produced high levels of inflammatory and anti-inflammatory proteins, with a high M1/M2 index. Macrophages on polyethylene terephthalate also resulted in a high M1/M2 index. Macrophages on Permacol™ produced a low amount of all proteins, with a low M1/M2 index. This model with human primary macrophages and the panel of read-out parameters can be used to evaluate the acute reaction of macrophages to biomaterials in vitro to get more insight in the foreign body reaction.

摘要

巨噬细胞在异物反应中起着重要作用。我们设计了一种使用人原代巨噬细胞的培养模型,以评估巨噬细胞对生物材料的急性反应。首先,我们通过暴露于 LPS+IFNγ 或 IL-4 来选择代表单核细胞促炎(M1)或抗炎/修复(M2)反应的蛋白质,从健康人类供体的血液中分离单核细胞。使用 IL-1β、IL-6、肿瘤坏死因子(TNF)α、单核细胞趋化蛋白(MCP)-3 和巨噬细胞炎性蛋白(MIP)-1α 作为 M1 标志物,以及白细胞介素-1 受体拮抗剂(IL-1RA)、CCL18、调节正常 T 细胞表达和分泌(RANTES)和巨噬细胞衍生趋化因子(MDC)作为 M2 标志物,计算相对 M1/M2 指数。然后,将单核细胞在 4 种已知具有不同异物反应的材料上培养 3 天:Permacol™、Parietex™ Composite、多丝聚对苯二甲酸乙二醇酯和多丝聚丙烯。聚丙烯上的巨噬细胞产生高水平的抗炎蛋白,M1/M2 指数较低。Parietex™ Composite 上的巨噬细胞产生高水平的促炎和抗炎蛋白,M1/M2 指数较高。聚对苯二甲酸乙二醇酯上的巨噬细胞也导致 M1/M2 指数较高。Permacol™上的巨噬细胞产生的所有蛋白质数量较少,M1/M2 指数较低。这种使用人原代巨噬细胞和检测参数面板的模型可用于评估巨噬细胞对生物材料的体外急性反应,以更深入了解异物反应。

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