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In vitro induction and differentiation of umbilical cord mesenchymal stem cells into neuron-like cells by alltrans retinoic acid

机译:全反式维甲酸体外诱导人脐带间充质干细胞分化为神经元样细胞

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AIM: To determine the optimal concentration for inducing the differentiation of human umbilical cord-derived mesenchymal stem cells(h UC-MSCs) into neuron-like cells, although it is understood that all-trans retinoic acid(ATRA) regulates cell proliferation in the nervous system by modulating the balance between mitosis and apoptosis.METHODS: The abilities of ATRA to promote apoptosis as well as neural differentiation were assessed in cultured h UC-MSCs by morphological observation, MTT assay, annexin V-FITC/PI flow cytometry and immunocytochemistry.RESULTS: The data showed that low concentrations of ATRA(0.5 μmol, 0.25 μmol) had no effect on the number of cells. However, treatment with 1.0 μmol or 2.0 μmol ATRA induced a 24.16% and 52.67% reduction in cell number, respectively, compared with vehicle-treated cultures. Further, 4.0 μmol ATRA had a potent effect on cell number, with almost no adherent cells recovered after 24 h. We further showed that 0.5 μmol ATRA caused these cells to express characteristic markers of neuronal progenitor cells.CONCLUSION: Taken together, we conclude that ATRA has a dose-dependent influence on the neural differentiation and apoptosis of h UC-MSCs. These findings have implications on the use of ATRA-differentiated h UC-MSCs for the study of neural degeneration diseases.
机译:目的:确定诱导人脐带间充质干细胞(h UC-MSCs)分化为神经元样细胞的最佳浓度,尽管据了解全反式维甲酸(ATRA)可调节人脐带间充质干细胞的增殖。方法:通过形态学观察,MTT测定,膜联蛋白V-FITC / PI流式细胞仪和免疫细胞化学评估培养的h UC-MSCs中ATRA促进细胞凋亡和神经分化的能力。结果:数据显示低浓度的ATRA(0.5μmol,0.25μmol)对细胞数量没有影响。但是,与媒介物处理的培养物相比,用1.0μmol或2.0μmolATRA处理分别诱导细胞数减少24.16%和52.67%。此外,4.0μmolATRA对细胞数量有很强的影响,在24 h后几乎没有粘附细胞恢复。我们进一步表明,0.5μmolATRA导致这些细胞表达神经元祖细胞的特征性标志。这些发现对使用ATRA分化的h UC-MSC用于神经退行性疾病的研究具有重要意义。

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