1 INEB-Instituto de Engenharia Biomédica, Universidade do Porto , Porto, Portugal .
Tissue Eng Part A. 2014 Jan;20(1-2):250-63. doi: 10.1089/ten.TEA.2012.0439. Epub 2013 Nov 14.
Macrophages are phagocytic cells with great importance in guiding multiple stages of inflammation and tissue repair. By producing a large number of biologically active molecules, they can affect the behavior of other cells and events, such as the foreign body response and angiogenesis. Since protein adsorption to biomaterials is crucial for the inflammatory process, we addressed the ability of the pro-inflammatory molecule fibrinogen (Fg) to modulate macrophage behavior toward tissue repair/regeneration. For this purpose, we used chitosan (Ch) as a substrate for Fg adsorption. Freshly isolated human monocytes were seeded on Ch substrates alone or previously adsorbed with Fg, and allowed to differentiate into macrophages for 10 days. Cell adhesion and morphology, formation of foreign body giant cells (FBGC), and secretion of a total of 80 cytokines and growth factors were evaluated. Both substrates showed similar numbers of adherent macrophages along differentiation as compared with RGD-coated surfaces, which were used as positive controls. Fg did not potentiate FBGC formation. In addition, actin cytoskeleton staining revealed the presence of punctuate F-actin with more elongated and interconnecting cells on Ch substrates. Antibody array screening and quantification of inflammation- and wound-healing-related factors indicated an overall reduction in Ch-based substrates versus RGD-coated surfaces. At late times, most inflammatory agents were down-regulated in the presence of Fg, in contrast to growth factor production, which was stimulated by Fg. Importantly, on Ch+Fg substrates, fully differentiated macrophages produced significant amounts of macrophage inflammatory protein-1delta (MIP-1δ), platelet-derived growth factor-BB, bone morphogenetic protein (BMP)-5, and BMP-7 compared with Ch alone. In addition, other important factors involved in bone homeostasis and wound healing, such as growth hormone, transforming growth factor-β3, and insulin-like growth factor-binding proteins, as well as several angiogenic mediators, including endocrine gland-derived vascular endothelial factor, fibroblast growth factor-7, and placental growth factor, were significantly promoted by Fg. This work provides a new perspective on the inflammatory response in the context of bone repair/regeneration mediated by a pro-inflammatory protein (Fg) adsorbed onto a biomaterial (Ch) that does not otherwise exhibit osteogenic properties.
巨噬细胞是吞噬细胞,在指导炎症和组织修复的多个阶段中具有重要作用。通过产生大量生物活性分子,它们可以影响其他细胞的行为和事件,如异物反应和血管生成。由于蛋白质吸附到生物材料对于炎症过程至关重要,因此我们研究了促炎分子纤维蛋白原(Fg)调节巨噬细胞向组织修复/再生行为的能力。为此,我们使用壳聚糖(Ch)作为 Fg 吸附的基质。新鲜分离的人单核细胞接种在单独的 Ch 基质上或先前吸附 Fg 的基质上,并允许其分化为巨噬细胞 10 天。评估细胞黏附与形态、异物巨细胞(FBGC)的形成以及总共 80 种细胞因子和生长因子的分泌情况。与用作阳性对照的 RGD 涂层表面相比,两种基质在分化过程中均显示出相似数量的黏附巨噬细胞。Fg 并未增强 FBGC 的形成。此外,肌动蛋白细胞骨架染色显示 Ch 基质上存在点状 F-肌动蛋白,细胞更加细长且相互连接。抗体阵列筛选和炎症及伤口愈合相关因子的定量分析表明,与 RGD 涂层表面相比,基于 Ch 的基质总体上减少了。在晚期,与生长因子的产生相反,在 Fg 存在的情况下,大多数炎症因子被下调。重要的是,在 Ch+Fg 基质上,完全分化的巨噬细胞产生了大量的巨噬细胞炎性蛋白-1 德尔塔(MIP-1δ)、血小板衍生生长因子-BB、骨形态发生蛋白(BMP)-5 和 BMP-7,而单独的 Ch 则没有。此外,其他与骨稳态和伤口愈合相关的重要因子,如生长激素、转化生长因子-β3 和胰岛素样生长因子结合蛋白,以及几种血管生成介质,包括内分泌腺衍生的血管内皮因子、成纤维细胞生长因子-7 和胎盘生长因子,也被 Fg 显著促进。这项工作为在促炎蛋白(Fg)吸附到不具有成骨特性的生物材料(Ch)的情况下介导的骨修复/再生背景下的炎症反应提供了新的视角。