首页> 外文期刊>Journal of King Saud University >Resolution factor 15-epi-Lipoxin A 4 modulates miRNA-499 induced differentiation of cardiosphere-derived stem cells through dual inhibition of Wnt/β-catenin and TGFβ/SMAD signalling axes
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Resolution factor 15-epi-Lipoxin A 4 modulates miRNA-499 induced differentiation of cardiosphere-derived stem cells through dual inhibition of Wnt/β-catenin and TGFβ/SMAD signalling axes

机译:分辨率因数15-Epi-ligoxin A 4 通过双重抑制Wnt /β-catenin和TGFβ/ Smad的双层抑制,调节MiRNA-499诱导的心脏源性干细胞分化 信号轴

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BackgroundCardiosphere derived stem cells (CDSCs) are signified as a valued source of stem cell therapeutics for treating a gamut of cardiovascular ailments. However, challenges in the cardiogenic differentiation process culminate in stem cell transplantation failure. Hence, it is imperative to understand the comprehensive mechanisms and the role of endogenous factors in cardiac differentiation.ObjectivesObjective of the current study is to check the effect of 15-epi-lipoxin A4(15E-LXA4)—a stable analogue of lipoxin A4, a pro-resolving agonist—on miR-499 (a cardiac-specific microRNA)-induced differentiation of CDSCs.MethodsCDSCs were transfected with lentiviral vectors bearing miR-499 and subjected to 15E-LXA4 treatment. Then, the treatment effects on surface markers (c-kit and CD105), cardiogenic gene markers (NKX2.5, GATA4, and cTnI), Wnt/β-catenin signaling (Wnt3a and phosphorylated/dephosphorylated β-catenin ratio) and TGFβ/SMAD signaling (TGFβ1 and SMAD3) were evaluated.Results15E-LXA4 treatment repressed miR-499 over-expression induced cardiac differentiation, manifested by enhanced expression of surface markers, Wnt/β-catenin and TGFβ/SMAD signaling parameters and reduced expression cardiogenic gene markers, plausibly through activation of estrogen receptor (ERα).ConclusionsThese findings give reason to understand the role of endogenous resolution factors like 15E-LXA4, as it displayed reciprocal effect on miR-499 induced cardiac differentiation in CDSCs.
机译:背景岩体衍生的干细胞(CDSCs)表示为治疗心血管疾病的色域的干细胞治疗剂的价值来源。然而,心绞痛分化过程中的挑战达到干细胞移植失败。因此,必须了解心脏分化内源性因素的综合机制和作用。目前研究的影响是检查15-EPI-脂蛋白A4(15E-LXA4)-A脂肪毒素A4稳定类似物的影响,将PRO-CONSTOMIS-ON MIR-499(一种心脏特异性MICRRNA)诱导CDSCS.metscs.methodcdscs的分化用携带miR-499的慢病毒载体转染并进行15e-Lxa4处理。然后,对表面标志物(C-kit和CD105)的治疗效果,心形成基因标记物(NKX2.5,GATA4和CTNI),WNT /β-连环蛋白信号传导(WNT3A和磷酸化/去磷酸化β-连环蛋白比率)和TGFβ/评估SMAD信号传导(TGFβ1和SMAD3)。结果15E-LXA4治疗抑制miR-499过表达诱导的心脏分解,表现出表面标志物,WNT /β-catenin和TGFβ/ smad信号传导参数的增强表达和表达式心源性基因标记,可编药通过激活雌激素受体(ERα)。结论的研究结果给出了理解,了解了15E-LXA4这样的内源性分辨率因子的作用,因为它显示了对CDSC中的miR-499诱导心脏分化的相互作用。

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