| Literature DB >> 27720607 |
Kotaro Sasaki1, Tomonori Nakamura1, Ikuhiro Okamoto1, Yukihiro Yabuta1, Chizuru Iwatani2, Hideaki Tsuchiya2, Yasunari Seita2, Shinichiro Nakamura2, Naoto Shiraki3, Tetsuya Takakuwa3, Takuya Yamamoto4, Mitinori Saitou5.
Abstract
The germ cell lineage ensures reproduction and heredity. The mechanism for germ cell specification in primates, including humans, has remained unknown. In primates, upon implantation the pluripotent epiblast segregates the amnion, an extra-embryonic membrane eventually ensheathing an embryo, and thereafter initiates gastrulation to generate three germ layers. Here, we show that in cynomolgus monkeys, the SOX17/TFAP2C/BLIMP1-positive primordial germ cells (cyPGCs) originate from the dorsal amnion at embryonic day 11 (E11) prior to gastrulation. cyPGCs appear to migrate down the amnion and, through proliferation and recruitment from the posterior amnion, expand in number around the posterior yolk sac by E17. Remarkably, the amnion itself expresses BMP4 and WNT3A, cytokines potentially critical for cyPGC specification, and responds primarily to them. Moreover, human PGC-like cells in vitro exhibit a transcriptome similar to cyPGCs just after specification. Our study identifies the origin of PGCs and a unique function of the nascent amnion in primates.Entities:
Keywords: BLIMP1; BMP4; SOX17; amnion; cynomolgus monkeys (Macaca fascicularis); epiblast; monkeys; primordial germ cells; specification
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Year: 2016 PMID: 27720607 DOI: 10.1016/j.devcel.2016.09.007
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270