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Bone morphogenetic protein 4 signaling regulates development of the anterior visceral endoderm in the mouse embryo

机译:骨形态发生蛋白4信号调节小鼠胚胎内脏内胚层的发育

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摘要

The extraembryonic ectoderm (ExE) of the mouse conceptus is known to play a role in embryo patterning by signaling to the underlying epiblast and surrounding visceral endoderm. Bmp4 is one of the key ExE signaling molecules and has been recently implicated to participate in regulating development and migration of the anterior visceral endoderm (AVE). However, it remains unclear when exactly BMP4 signaling starts to regulate AVE positioning. To examine this, we have chosen to affect BMP4 function at two different time points, at embryonic day 5.25 (E5.25), thus before AVE migration, and E5.75, just after AVE migration. To this end, an RNAi technique was used, which consisted of the injection of Bmp4 dsRNA into the proamniotic cavity of the egg cylinder followed by its targeted electroporation into the ExE. This resulted in specific knockdown of Bmp4. It was found that Bmp4 RNAi at E5.25, but not at E5.75, led to an abnormal pattern of expression of the AVE marker Cerberus-like. Thus, BMP4 signaling appears to affect the expression of Cer1 at a specific time window. This RNAi approach provides a convenient means to study spatial and temporal function of genes shortly after embryo implantation.
机译:已知小鼠概念的胚外外胚层(ExE)通过向下面的上皮细胞和周围内脏内胚层发信号来在胚胎构型中发挥作用。 Bmp4是关键的ExE信号分子之一,最近被认为参与调节前内脏内胚层(AVE)的发育和迁移。但是,尚不清楚确切的BMP4信号何时开始调节AVE定位。为了检查这一点,我们选择在两个不同的时间点,即在AVE迁移之前的第5.25天(E5.25)和E5.75(在AVE迁移之后)影响BMP4的功能。为此,使用了一种RNAi技术,该技术包括将Bmp4 dsRNA注入卵瓶的羊膜腔中,然后将其靶向电穿孔进入ExE。这导致Bmp4的特异性敲低。发现在E5.25处而不是在E5.75处的Bmp4 RNAi导致AVE标志物类Cerberus样表达的异常模式。因此,BMP4信号似乎在特定的时间窗口会影响Cer1的表达。这种RNAi方法为胚胎植入后不久研究基因的时空功能提供了便利的手段。

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