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首页> 外文期刊>Stem cells and development >Improved establishment of autologous stem cells derived from preantral follicle culture and oocyte parthenogenesis.
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Improved establishment of autologous stem cells derived from preantral follicle culture and oocyte parthenogenesis.

机译:改进的建立自前壁卵泡培养和卵母细胞孤雌生殖的自体干细胞的建立。

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This study was conducted to improve establishing autologous embryonic stem cells (ESCs) by culture of preantral follicles and parthenogenetic activation of oocytes. First, paternal inheritance of the follicle donor was changed without altering maternal heredity by employing B6CBAF1 instead of B6D2F1 mice. A significant increase in the establishment of parthenogenetic ESCs was detected after the change, and a different gene expression pro-file was detected in the ESCs established. Among 62 stemness-related genes showing different expression level between two strains, 35 (56.5%) were lower in the rarely established ESCs (B6D2F1) than in the easily established ESCs (B6CBAF1). Several paternally expressed genes were aberrantly expressed in the rarely established ESCs. Second, the establishment of parthenogenetic ESCs in B6D2F1 was significantly improved when preantral follicles were cultured in glutathione (GSH)-containing medium. In the ESCs derived from GSH-treated follicles, 77% of the 62 genes showing the difference increased their expression. Translation of several proteins related to stemness (Wnt-1, beta-catenin, p-p44/42, and smad) was similar between the parthenogenetic ESCs established after GSH treatment and the control E14 ESCs. We concluded that change in genetic inheritance and exposure of in vitro-growing ovarian follicles to GSH contributes to improving establishment of parthenogenetic ESCs, which may help increase the feasibility of the established lines for patient-specific, stem cell therapy.
机译:这项研究的目的是通过培养前壁卵泡和卵母细胞的孤雌性活化来改善自体胚胎干细胞(ESC)的建立。首先,通过使用B6CBAF1代替B6D2F1小鼠,在不改变母体遗传的情况下改变了卵泡供体的父本遗传。更改后,检测到孤雌生殖ESC的建立显着增加,并且在建立的ESC中检测到不同的基因表达原文件。在两个菌株之间显示不同表达水平的62个干性相关基因中,很少建立的ESC(B6D2F1)中的35个(56.5%)低于容易建立的ESC(B6CBAF1)。几个父系表达的基因在极少建立的ESC中异常表达。其次,当在含谷胱甘肽(GSH)的培养基中培养前窦卵泡时,B6D2F1中孤雌生殖ESC的建立显着改善。在由GSH处理的卵泡衍生的ESC中,显示差异的62个基因中有77%增加了它们的表达。在GSH处理后建立的孤雌生殖ESC与对照E14 ESC之间,与干性相关的几种蛋白质(Wnt-1,β-catenin,p-p44 / 42和smad)的翻译相似。我们得出的结论是,遗传继承的改变和体外生长的卵巢卵泡对GSH的暴露有助于改善孤雌生殖ESC的建立,这可能有助于增加针对特定患者的干细胞疗法建立的系的可行性。

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