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Selective depletion of cultured macrophages by magnetite nanoparticles modified with gelatin

机译:明胶修饰的磁铁矿纳米颗粒对培养巨噬细胞的选择性消耗

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摘要

Previous studies have indicated pro-tumor functions of macrophages in tumor progression in different types of malignant tumors. The detailed mechanisms of cell-cell interaction between macrophages and tumor cells have been investigated by means of in vitro co-culture experiments. The present study developed magnetite nanoparticles modified with gelatin that are specifically engulfed by macrophages and investigated methods to deplete these macrophages in co-culture experiments using a magnet. T98G glioma cell line and human monocyte-derived macrophages were mixed and co-cultured for 2 days. The T98G cells were isolated by depletion of the macrophages using the magnetite nanoparticles. mRNA expression of a number of pro-tumor molecules in the isolated T98G cells, with or without co-culture with macrophages, was then evaluated. The mRNA expression levels of chemokine (CC motif) ligand 2, interleukin-6 and macrophage-colony stimulating factor receptor (M-CSFR) were significantly upregulated in T98G cells by co-culture with macrophages (P<0.01). M-CSFR protein expression was also increased by co-culture with macrophages. The conditioned medium of co-cultured cells increased M-CSFR expression in T98G cells. Magnetite nanoparticles may be a novel tool not only for investigating the unique activation status of tumor cells in co-culture conditions, but also for targeting pro-tumor macrophages in tumor tissues.
机译:先前的研究表明巨噬细胞在不同类型的恶性肿瘤中在肿瘤进展中的促肿瘤功能。已经通过体外共培养实验研究了巨噬细胞和肿瘤细胞之间的细胞间相互作用的详细机制。本研究开发了明胶修饰的磁铁矿纳米颗粒,它们被巨噬细胞特异性吞噬,并研究了在使用磁体的共培养实验中耗尽这些巨噬细胞的方法。将T98G神经胶质瘤细胞系和人单核细胞衍生的巨噬细胞混合并共培养2天。通过使用磁铁矿纳米颗粒消耗巨噬细胞来分离T98G细胞。然后评估在分离的T98G细胞中有或没有与巨噬细胞共培养的许多促肿瘤分子的mRNA表达。通过与巨噬细胞共培养,T98G细胞中趋化因子(CC基序)配体2,白介素6和巨噬细胞集落刺激因子受体(M-CSFR)的mRNA表达水平显着上调(P <0.01)。通过与巨噬细胞共培养,M-CSFR蛋白表达也增加。共培养细胞的条件培养基可提高T98G细胞中M-CSFR的表达。磁铁矿纳米粒子可能是一种新颖的工具,不仅可以用于研究共培养条件下肿瘤细胞的独特活化状态,而且可以用于靶向肿瘤组织中的肿瘤前巨噬细胞。

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