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hUMSC transplantation restores ovarian function in POI rats by inhibiting autophagy of theca-interstitial cells via the AMPK/mTOR signaling pathway

机译:HUMSC移植通过通过AMPK / MTOR信号通路抑制THCA-Intriteial细胞的自噬恢复Poi大鼠的卵巢功能

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Previous studies of primary ovarian insufficiency (POI) have focused on granulosa cells (GCs) and ignored the role of theca-interstitial cells (TICs). This study aims to explore the mechanism of the protective effects of human umbilical cord-derived mesenchymal stem cells (hUMSCs) on ovarian function in POI rats by regulating autophagy of TICs. The POI model was established in rats treated with cisplatin (CDDP). The hUMSCs were transplanted into POI rats by tail vein. Enzyme-linked immunosorbent assay (ELISA) analysis, hematoxylin and eosin (HE) staining, and immunohistochemistry were used to measure the protective effects of hUMSCs. The molecular mechanisms of injury and repairment of TICs were assessed by immunofluorescence, transmission electron microscope (TEM), flow cytometry (FCM), western blot, and quantitative real-time polymerase chain reaction (qRT-PCR). In vivo, hUMSC transplantation restored the ovarian function and alleviated the apoptosis of TICs in POI rats. In vitro, hUMSCs reduced the autophagy levels of TICs by reducing oxidative stress and regulating AMPK/mTOR signaling pathway, thereby alleviating the apoptosis of TICs. This study indicates that hUMSCs protected ovarian function in POI by regulating autophagy signaling pathway AMPK/mTOR.
机译:以前对原发性卵巢功能不全(POI)的研究集中在颗粒细胞(GCS)上,并忽略了Theca-Intertitien细胞(TICS)的作用。本研究旨在通过调节TICS的自噬来探讨人脐带衍生间充质干细胞(HUMSCS)对POI大鼠卵巢功能的保护作用的机制。在用顺铂(CDDP)处理的大鼠中建立了POI模型。通过尾静脉移植到Poi大鼠中。酶联免疫吸附测定(ELISA)分析,血液杂环和曙红(HE)染色,免疫组化用于测量HUMSCs的保护作用。通过免疫荧光,透射电子显微镜(TEM),流式细胞术(FCM),蛋白质印迹和定量实时聚合酶链反应(QRT-PCR)评估TICs损伤和修复修复的分子机制。体内,HUMSC移植恢复了卵巢功能,减轻了POI大鼠TIC的凋亡。体外,通过减少氧化应激和调节AMPK / MTOR信号传导途径来减少TICS的自噬水平,从而减轻了TIC的凋亡。本研究表明,通过调节自噬信号通路AMPK / MTOR,HUMSCS在POI中受到保护的卵巢功能。

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