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近端脏内胚层和胚外外胚层调节原始生殖细胞前体的形成。

Proximal visceral endoderm and extraembryonic ectoderm regulate the formation of primordial germ cell precursors.

作者信息

de Sousa Lopes Susana M Chuva, Hayashi Katsuhiko, Surani M Azim

机构信息

The Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.

出版信息

BMC Dev Biol. 2007 Dec 20;7:140. doi: 10.1186/1471-213X-7-140.

Abstract

BACKGROUND

The extraembryonic tissues, visceral endoderm (VE) and extraembryonic ectoderm (ExE) are known to be important for the induction of primordial germ cells (PGCs) in mice via activation of the bone morphogenetic protein (BMP) signalling pathway. We investigated whether the VE and ExE have a direct role in the specification of PGCs, or in an earlier event, namely the induction of the PGC precursors in the proximal posterior epiblast cells.

RESULTS

We cultured embryonic day (E) 5.75 to E7.0 mouse embryos in an explant-assay with or without extraembryonic tissues. The reconstituted pieces of embryonic and extraembryonic tissues were assessed for the formation of both PGC precursors and specified PGCs. For this, Blimp1:gfp and Stella:gfp transgenic mouse lines were used to distinguish between PGC precursors and specified PGC, respectively. We observed that the VE regulates formation of an appropriate number of PGC precursors between E6.25-E7.25, but it is not essential for the subsequent specification of PGCs from the precursor cells. Furthermore, we show that the ExE has a different role from that of the VE, which is to restrict localization of PGC precursors to the posterior part of the embryo.

CONCLUSION

We show that the VE and ExE have distinct roles in the induction of PGC precursors, namely the formation of a normal number of PGC precursors, and their appropriate localization during early development. However, these tissues do not have a direct role during the final stages of specification of the founder population of PGCs.

摘要

背景

已知胚胎外组织,即脏内胚层(VE)和胚胎外胚层(ExE),通过激活骨形态发生蛋白(BMP)信号通路,在小鼠原始生殖细胞(PGC)的诱导中发挥重要作用。我们研究了VE和ExE在PGC特化过程中是否具有直接作用,或者在更早的事件中,即在近端后胚层细胞中PGC前体的诱导过程中是否具有直接作用。

结果

我们在有或没有胚胎外组织的外植体试验中培养了胚胎第(E)5.75至E7.0天的小鼠胚胎。对重组的胚胎和胚胎外组织块进行PGC前体和特化PGC形成的评估。为此,分别使用Blimp1:gfp和Stella:gfp转基因小鼠品系来区分PGC前体和特化PGC。我们观察到,VE在E6.25 - E7.25之间调节适当数量的PGC前体的形成,但对于随后从前体细胞特化PGC来说并非必需。此外,我们表明ExE的作用与VE不同,它是将PGC前体的定位限制在胚胎后部。

结论

我们表明,VE和ExE在PGC前体的诱导中具有不同作用,即正常数量PGC前体的形成以及它们在早期发育过程中的适当定位。然而,这些组织在PGC创始群体特化的最后阶段没有直接作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f1/2231376/536eddc7a509/1471-213X-7-140-1.jpg

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