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首页> 外文期刊>International Journal of Molecular Sciences >Enhancement of Anti-Hypoxic Activity and Differentiation of Cardiac Stem Cells by Supernatant Fluids from Cultured Macrophages that Phagocytized Dead Mesenchymal Stem Cells
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Enhancement of Anti-Hypoxic Activity and Differentiation of Cardiac Stem Cells by Supernatant Fluids from Cultured Macrophages that Phagocytized Dead Mesenchymal Stem Cells

机译:吞噬死的间充质干细胞的培养巨噬细胞上清液的增强抗缺氧活性和干细胞的分化。

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Background: Most mesenchymal stem cells (MSCs) die shortly after transplantation into a myocardial infarcted area. Dead MSCs (dMSCs) are phagocytized by macrophages (pMΦ) in vivo and in vitro; however, the effects of pMΦ on cardiac stem cells (CSCs) remain unknown. Methods: MSCs, CSCs, and macrophages were obtained from bone marrow, hearts, and peritoneal cavity of mice, respectively. dMSCs were harvested after hypoxia for 24 h, and incubated with macrophages (2:1) for another 2 days with or without lipopolysaccharide (LPS, 50 ng/mL) and sorted by flow cytometry to obtain pMΦ. Viability and apoptosis of CSCs were respectively evaluated with the cell counting kit-8 (CCk-8) assay and Annexin V-PE/7-AAD staining at 0, 6, 12, and 24 h of culture with supernatant fluids from macrophages (MΦ), LPS-stimulated macrophages (LPS-pMΦ), pMΦ, and MSCs. GATA-4 and c-TnI expression was measured by flow cytometry on the seventh day. Expression of inflammation and growth factors was assessed by real-time polymerase chain reaction (RT-PCR) in MΦ, LPS-pMΦ, and pMΦ cells. Results: pMΦ expressed higher levels of interleukin-10 (IL-10) and transforming growth factor-β (TGF-β)and lower levels of tumor necrosis factor-α(TNF-α)and IL-6 than LPS-pMΦ, higher levels of growth factors and of GATA-4 and c-TnI at the 7th day, which were similar to those in MSCs. CSCs cultured with supernatant fluids of pMΦ exhibited higher proliferative, anti-hypoxic, and differentiation activities. Conclusion: The supernatant fluids of macrophages that had phagocytized dead MSCs encouraged changes in phenotype and growth factor expression, enhanced proliferation, differentiation, and anti-hypoxic activity of CSCs, which is relevant to understanding the persistent therapeutic effect of MSCs after their massive demise upon transplantation in myocardial infarction. Furthermore, some miRNAs or proteins which were extracted from the supernatant fluids may give us a new insight into the treatment of myocardial infarction in the future.
机译:背景:大多数间充质干细胞(MSCs)移植到心肌梗塞区域后不久就会死亡。体内和体外巨噬细胞(pMΦ)吞噬死亡的MSC(dMSC)。然而,pMΦ对心脏干细胞(CSCs)的影响仍然未知。方法:分别从小鼠的骨髓,心脏和腹膜腔获得MSCs,CSCs和巨噬细胞。缺氧24小时后收集dMSC,并在有或没有脂多糖(LPS,50 ng / mL)的情况下与巨噬细胞(2:1)再孵育2天,并通过流式细胞仪分选以获得pMΦ。用细胞计数试剂盒8(CCk-8)检测和膜联蛋白V-PE / 7-AAD染色分别在巨噬细胞(MΦ)上清液培养0、6、12和24 h时评估CSC的活力和凋亡),LPS刺激的巨噬细胞(LPS-pMΦ),pMΦ和MSC。在第七天通过流式细胞术测量GATA-4和c-TnI表达。通过实时聚合酶链反应(RT-PCR)在MΦ,LPS-pMΦ和pMΦ细胞中评估炎症和生长因子的表达。结果:与LPS-pMΦ相比,pMΦ表达白细胞介素10(IL-10)和转化生长因子-β(TGF-β)的水平更高,而肿瘤坏死因子-α(TNF-α)和IL-6的水平则更低,第7天的生长因子以及GATA-4和c-TnI的水平与MSC中的水平相似。用pMΦ上清液培养的CSC表现出更高的增殖,抗缺氧和分化活性。结论:吞噬了死亡MSC的巨噬细胞的上清液促进了CSC的表型和生长因子表达的改变,增强了CSC的增殖,分化和抗缺氧活性,这与了解MSC在大量死亡后的持续治疗效果有关。心肌梗死的移植。此外,从上清液中提取的一些miRNA或蛋白质可能为我们将来对心肌梗塞的治疗提供新的见解。

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