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在有袋动物,Monodelphis domestica Wagner 的胚胎中,Oct4、Cdx2、Tead4 和 Yap1 蛋白在囊胚形成过程中的表达模式。

Expression patterns of Oct4, Cdx2, Tead4, and Yap1 proteins during blastocyst formation in embryos of the marsupial, Monodelphis domestica Wagner.

机构信息

Department of Biology, Oberlin College, Oberlin, OH 44074, USA.

出版信息

Evol Dev. 2013 May;15(3):171-85. doi: 10.1111/ede.12031.

Abstract

The marsupial blastocyst forms in an entirely different manner from its eutherian counterpart, involving cell-zona rather than cell-cell adhesion during the 8- to-16-cell transition. While the eutherian blastocyst consists of a spherical trophoblast completely enveloping a pluripotent inner cell mass, or pluriblast, the marsupial blastocyst forms initially as a bowl-shaped monolayer of cells lining the zona pellucida at the embryonic pole (ep). This monolayer contains a small patch of centrally positioned pluriblast cells edged with trophoblast cells that later coalesce at the abembryonic pole. Using immunocytochemistry, we examined the localization of the proteins Oct4, Cdx2, Tead4, Sox2, and Yap1 in opossum embryos to determine if their temporal expression pattern differed from that in the mouse, given the important differences in cell behavior preceding blastocyst formation in these mammals. Our results indicate that these proteins are expressed in similar temporal patterns despite the topological differences between mouse and opossum cleavage-stage embryos and blastocysts. That the Hippo-pathway protein Yap1 localized specifically around the approximately 128-cell stage to opossum trophoblast nuclei but remained in the cytoplasm of pluriblast cells suggests that this transcriptional regulator participates in allocating cells to the trophoblast lineage, as it does in mouse. Interestingly, in both mouse and opossum embryos, expression of the pluripotency marker Oct4 persisted after Cdx2, which signals trophoblast specification, began to be expressed in trophoblast cells. This and the observation that Cdx2 is present in opossum embryos well before blastomere-zona adhesion even occurs suggests that the proteins studied may have other roles in early mammalian embryonic development.

摘要

有袋类动物的囊胚以完全不同的方式形成,与有胎盘哺乳动物相比,在 8-16 细胞期过渡过程中涉及细胞-透明带而不是细胞-细胞黏附。虽然有胎盘哺乳动物的囊胚由完全包围多能内细胞团或多能细胞的球形滋养层组成,但有袋类动物的囊胚最初形成一个碗状单层细胞,排列在胚胎极(ep)的透明带上。这个单层细胞包含一个中央位置的多能细胞小块,边缘是滋养层细胞,这些细胞后来在原肠胚极(abembryonic pole)融合。我们使用免疫细胞化学技术检查了负鼠胚胎中 Oct4、Cdx2、Tead4、Sox2 和 yap1 蛋白的定位,以确定它们的时空表达模式是否与小鼠不同,因为在这些哺乳动物中,囊胚形成前的细胞行为存在重要差异。我们的结果表明,尽管小鼠和负鼠卵裂期胚胎和囊胚的拓扑结构存在差异,但这些蛋白的表达模式相似。Hippo 通路蛋白 yap1 特异性定位于大约 128 细胞期的负鼠滋养层细胞核,但仍位于多能细胞的细胞质中,这表明该转录调节剂参与将细胞分配到滋养层谱系中,就像在小鼠中一样。有趣的是,在小鼠和负鼠胚胎中,多能性标记物 Oct4 的表达在 Cdx2 开始在滋养层细胞中表达后仍然持续,Cdx2 信号提示滋养层特化。这一观察结果以及 Cdx2 甚至在卵裂球-透明带黏附之前就存在于负鼠胚胎中,表明所研究的蛋白可能在早期哺乳动物胚胎发育中具有其他作用。

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