首页> 美国卫生研究院文献>The Journal of Reproduction and Development >Lipofection of siRNA into bovine 8-16-cell stage embryos using zona removal and the well-of-the-well culture system
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Lipofection of siRNA into bovine 8-16-cell stage embryos using zona removal and the well-of-the-well culture system

机译:使用透明带去除法和井间培养系统将siRNA脂转染到牛8-16细胞期胚胎中

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摘要

Bovine preimplantation embryos exhibit dramatic biological changes between before and after the 8-16-cell stage. Here we report a simple lipofection method to transfect siRNA into bovine 8-16-cell stage embryos using zona removal and the well-of-the-well (WOW) culture system. Bovine one-cell embryos produced in vitro were freed from the zona pellucida and cultured up to the 8-16-cell stage in WOW dishes. The 8-16-cell embryos were lipofected with siRNA and the transfection efficiency was assessed at 48 h of transfection. Lipofection with a red fluorescent non-targeting siRNA revealed the importance of zona removal for transfection of siRNA into embryos. Using this method, we knocked down the methionine adenosyltransferase 2A (MAT2A) gene, achieving a significant reduction in MAT2A expression (P < 0.05) concomitant with the marked inhibition of blastocyst development. Our proposed method, tentatively named ‘Octo-lipofection’, may be useful to analyze gene functions in bovine preimplantation embryos without expensive equipment and skill-intensive techniques.
机译:牛植入前胚胎在8-16细胞阶段之前和之后显示出显着的生物学变化。在这里,我们报告了一种简单的脂质转染方法,可使用透明带去除法和井上培养(WOW)培养系统将siRNA转染到牛8-16细胞期胚胎中。将体外产生的牛单细胞胚胎从透明带中取出,并在WOW皿中培养至8-16细胞阶段。将8-16细胞的胚胎用siRNA脂质转染,并在转染48小时后评估转染效率。用红色荧光非靶向siRNA脂质转染揭示了去除透明带对于将siRNA转染到胚胎中的重要性。使用这种方法,我们敲低了蛋氨酸腺苷转移酶2A(MAT2A)基因,实现了MAT2A表达的显着降低(P <0.05),并显着抑制了胚泡的发育。我们提议的方法暂时称为“ Octo-lipofection”,可能对分析牛植入前胚胎中的基因功能有用,而无需昂贵的设备和技术密集的技术。

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