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三种浓度视黄酸诱导绵羊骨髓间充质干细胞向雄性生殖细胞转分化的疗效比较

Comparison of the efficacy of three concentrations of retinoic acid for transdifferentiation induction in sheep marrow-derived mesenchymal stem cells into male germ cells.

作者信息

Ghasemzadeh-Hasankolaei M, Eslaminejad M B, Batavani R, Sedighi-Gilani M

机构信息

Department of Clinical Sciences, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.

Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.

出版信息

Andrologia. 2014 Feb;46(1):24-35. doi: 10.1111/and.12037. Epub 2012 Nov 7.

Abstract

Recent studies have shown the unique role of retinoic acid (RA) in the induction of transdifferentiation in mesenchymal stem cells (MSCs) into germ cells (GCs). This study is the first study that compares the efficacy of three different concentrations of RA for the production of male GCs in vitro. Male sheep marrow-derived MSCs (MMSCs) were treated with the following concentrations of RA: 1 μm (RA1), 5 μm (RA2) and 10 μm (RA3) for a period of 21 days. The production of male GCs was evaluated by the assessment of expressions of GC-specific markers (by RT-PCR, qRT-PCR and immunocytochemistry), morphological characteristics and changes in alkaline phosphatase (ALP) activity. All three concentrations created male GC features. RA treatment upregulated the expressions of VASA and beta1 INTEGRIN and downregulated PIWIL2 and OCT4. DAZL was not expressed by RA treatment. Interestingly, immunocytochemistry detected PGP 9.5 expression in all treatment groups, with the highest expression noted in the RA3 group (P < 0.05). GC-like cells along with increased ALP activity were observed in all treated cultures, too. Finally, results showed that 10 μm RA has the most efficiency for transdifferentiation induction in MMSCs and production of male GCs in vitro.

摘要

近期研究表明,视黄酸(RA)在诱导间充质干细胞(MSC)向生殖细胞(GC)转分化过程中发挥着独特作用。本研究首次比较了三种不同浓度的RA在体外诱导产生雄性GC的效果。用以下浓度的RA处理雄性绵羊骨髓来源的MSC(MMSC):1μm(RA1)、5μm(RA2)和10μm(RA3),处理21天。通过评估GC特异性标志物的表达(采用逆转录聚合酶链反应、定量逆转录聚合酶链反应和免疫细胞化学法)、形态特征以及碱性磷酸酶(ALP)活性变化来评价雄性GC的产生情况。所有三种浓度均产生了雄性GC特征。RA处理上调了VASA和β1整合素的表达,下调了PIWIL2和OCT4的表达。RA处理未检测到DAZL的表达。有趣的是,免疫细胞化学检测发现所有处理组均有PGP 9.5表达,其中RA3组表达最高(P<0.05)。在所有处理的培养物中也观察到了类GC细胞以及ALP活性增加。最后,结果表明10μm RA在体外诱导MMSC向雄性GC转分化方面效率最高。

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