King Suzanne N, Hanson Summer E, Chen Xia, Kim Jaehyup, Hematti Peiman, Thibeault Susan L
Division of Otolaryngology - Head and Neck Surgery, University of Wisconsin-Madison, Madison, Wisconsin.
J Biomed Mater Res A. 2014 Mar;102(3):890-902. doi: 10.1002/jbm.a.34746. Epub 2013 Jun 24.
Macrophages play a critical role in mediating not only normal tissue healing, but also the host reaction against biomaterial scaffolds. There is increasing interest in regenerative medicine to combine mesenchymal stromal/stem cells (MSCs) with biomaterial scaffolds to modulate inflammatory response while restoring tissue architecture. The objective of the current study was to investigate the interaction between MSCs (derived from bone marrow, adipose or vocal fold tissue) encapsulated in hyaluronan-based hydrogel and differentiating macrophages as measured by extracellular matrix (ECM) gene expression and cytokine, chemokine, and growth factor concentrations. Gene expression was analyzed using real-time polymerase chain reaction from MSCs embedded in Carbylan-GSX after 7 days of coculture with or without CD14+ cells. Protein concentrations were measured using a Bio-plex assay from cell culture supernatants on days 3 and 7 for all conditions. Following 7 days, we identified upregulation of collagen-I, collagen-III, procollagen, and matrix metalloproteinase-9 genes compared to control conditions. We demonstrate increased concentrations of immunoregulatory cytokines [interleukin (IL)-1β, tumor necrosis factor-α, macrophage inflammatory protein-1α, IFN-γ, IL-12, and IL-10] and remodeling growth factors (vascular endothelial growth factor, hepatocyte growth factor) in MSC-3D constructs cocultured with macrophages compared to control conditions, with some temporal variation. Our results indicate an alteration of expression of ECM proteins important to tissue regeneration and cytokines critical to the inflammatory cascade when 3D constructs were cultured with differentiating macrophages.
巨噬细胞不仅在介导正常组织愈合中发挥关键作用,而且在宿主对生物材料支架的反应中也起着关键作用。再生医学领域越来越关注将间充质基质/干细胞(MSCs)与生物材料支架相结合,以调节炎症反应并恢复组织结构。本研究的目的是通过细胞外基质(ECM)基因表达以及细胞因子、趋化因子和生长因子浓度,研究包裹在透明质酸基水凝胶中的MSCs(来源于骨髓、脂肪或声带组织)与分化中的巨噬细胞之间的相互作用。在与CD14+细胞共培养7天之后,使用实时聚合酶链反应对嵌入Carbylan - GSX中的MSCs进行基因表达分析。在所有条件下,于第3天和第7天使用Bio - plex分析法定量测定细胞培养上清液中的蛋白质浓度。7天后,我们发现与对照条件相比,I型胶原、III型胶原、前胶原和基质金属蛋白酶-9基因上调。我们证明,与对照条件相比,与巨噬细胞共培养的MSCs三维构建体中免疫调节细胞因子[白细胞介素(IL)-1β、肿瘤坏死因子-α、巨噬细胞炎性蛋白-1α、干扰素-γ、IL-12和IL-10]以及重塑生长因子(血管内皮生长因子、肝细胞生长因子)的浓度增加,且存在一定的时间差异。我们的结果表明,当三维构建体与分化中的巨噬细胞一起培养时,对组织再生重要的ECM蛋白表达以及对炎症级联反应至关重要的细胞因子发生了改变。