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首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >Expression analysis of PAWP during mouse embryonic stem cell-based spermatogenesis in vitro
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Expression analysis of PAWP during mouse embryonic stem cell-based spermatogenesis in vitro

机译:PAWP在小鼠胚胎干细胞体外精子发生过程中的表达分析

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摘要

Postacrosomal sheath WW domain-binding protein (PAWP) is a novel sperm protein identified as a candidate sperm-borne, oocyte-activating factor (SOAF). However, regulation of PAWP gene expression is poorly understood. Therefore, we examined the PAWP gene expression across different stages of mouse embryonic stem cell (ESC)-based spermatogenesis in vitro and compared this expression at different stages of mouse testis development in vivo. Expression of PAWP was also examined in mouse embryonic fibroblasts (MEF), Sertoli cell, and the NIH3T3 cancerous cell line. We used a transgenic mouse ESC line C57BL/6J expressing Stra8-EGFP that was plated in murine ESC medium. To induce differentiation, cells were cultured on gelatin-coated medium with Retinoic Acid (RA) treatment. We applied reverse transcription-PCR and real-time PCR to analyze the differential expression of PAWP mRNA during different stages of mouse ESC differentiation in vitro parallel with mouse testis development in vivo and in cell lines. We found that expression of PAWP is increased during testis development in vivo with greatest expression at postmeiotic phase. It is also highly expressed in mouse ESC-derived germ-like cells after 30 d of RA induction in vitro. PAWP is remarkably expressed in mouse ESC and NIH3T3 cell line. These results indicate that PAWP plays a role in spermatogenesis and germ cell development. Moreover, we suggest PAWP as one of the markers that could be looked in ESC studies as a confirmed testis-specific gene. We also suggest an additional possible role for PAWP in proliferation of cancerous cell in general.
机译:顶体后鞘WW域结合蛋白(PAWP)是一种新型的精子蛋白,被鉴定为候选的精子携带的卵母细胞激活因子(SOAF)。但是,对PAWP基因表达的调控了解甚少。因此,我们在体外基于小鼠胚胎干细胞(ESC)的精子发生的不同阶段检查了PAWP基因表达,并在小鼠体内睾丸发育的不同阶段比较了该表达。还检查了小鼠胚胎成纤维细胞(MEF),Sertoli细胞和NIH3T3癌细胞系中PAWP的表达。我们使用了表达Stra8-EGFP的转基因小鼠ESC系C57BL / 6J,将其接种在鼠ESC培养基中。为了诱导分化,将细胞在经视黄酸(RA)处理的明胶包被的培养基上进行培养。我们应用逆转录PCR和实时PCR分析PAWP mRNA在小鼠胚胎干细胞分化的不同阶段在体外与小鼠睾丸在体内和细胞系中的发育过程中的差异表达。我们发现,PAWP的表达在体内睾丸发育过程中增加,减数分裂后阶段的表达最大。在体外RA诱导30 d后,它在小鼠ESC来源的生殖样细胞中也高表达。 PAWP在小鼠ESC和NIH3T3细胞系中显着表达。这些结果表明PAWP在精子发生和生殖细胞发育中起作用。此外,我们建议PAWP作为可在ESC研究中视为已证实的睾丸特异性基因的标志物之一。我们还建议一般而言,PAWP在癌细胞增殖中的其他可能作用。

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