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Effects of platelet-rich plasma on the activity of human menstrual blood-derived stromal cells in vitro

机译:富血小板血浆对人经血来源基质细胞体外活性的影响

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摘要

Human menstrual blood-derived stromal cells (MenSCs) are highly proliferative and show multiple differentiation capacity. The convenience and non-invasiveness make MenSC a novel cell source for regenerative medicine applications. Platelet-rich plasma (PRP) contains abundant growth factors which are beneficial to wound healing. However, the influence of PRP on MenSCs remains elusive. Here, we evaluated the role of PRP in MenSCs proliferation and assessed the effects of PRP on endometrial receptivity regulation in vitro. MenSCs cultured with 10% activated PRP were compared with those cultured with 10% fetal bovine serum (FBS). Differences in cell proliferation, differentiation, and endometrial receptivity-related gene expression were evaluated. Notably, 10% activated PRP significantly promoted MenSCs proliferation and adipogenic/osteogenic differentiation while suppressing apoptosis. Expression of the mesenchymal stem cells (MSCs) marker CD105 and the perivascular markers SUSD2 and CD146 were elevated after PRP treatment. Moreover, short-term PRP stimulation activated the phosphorylation of Akt and signal transducer and activator of transcription 3 (STAT3) pathways, upregulated expression of FoxO1, LIF, and IL1-β, and downregulated IL-6. In summary, PRP could promote MenSC proliferation, markedly accelerate cell stemness, and evaluate MenSC functions by enhancing the expression of angiogenesis and endometrial receptivity markers, suggesting its potential use as a promising supplement for MenSCs in endometrial regenerative medicine. Our results provide a theoretical basis for the clinical application of co-transplantation of PRP combined with MenSCs.
机译:人经血来源的基质细胞(MenSCs)高度增殖,并显示出多种分化能力。 MenSC的便利性和非侵入性使其成为再生医学应用的新型细胞来源。富含血小板的血浆(PRP)含有丰富的生长因子,有利于伤口愈合。但是,PRP对MenSC的影响仍然难以捉摸。在这里,我们评估了PRP在MenSCs增殖中的作用,并评估了PRP对体外子宫内膜容受性调节的影响。将用10%活化PRP培养的MenSCs与用10%胎牛血清(FBS)培养的MenSCs进行比较。评估了细胞增殖,分化和子宫内膜接受性相关基因表达的差异。值得注意的是,10%活化的PRP可显着促进MenSCs增殖和成脂/成骨分化,同时抑制细胞凋亡。 PRP处理后,间充质干细胞(MSCs)标记CD105以及血管周标记SUSD2和CD146的表达升高。此外,短期PRP刺激激活了Akt的磷酸化以及信号转导和转录激活因子3(STAT3)的通路,FoxO1,LIF和IL1-β的表达上调,而IL-6的表达下调。总之,PRP可以通过增强血管生成和子宫内膜容受性标志物的表达来促进MenSC的增殖,显着加速细胞干,并评估MenSC的功能,表明其潜在用途可作为MenSC在子宫内膜再生医学中的有希望的补充。我们的结果为PRP与MenSCs联合移植的临床应用提供了理论依据。

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