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终身体内细胞谱系追踪表明,成年小鼠的卵子发生并非源自假定的生殖系干细胞。

Life-long in vivo cell-lineage tracing shows that no oogenesis originates from putative germline stem cells in adult mice.

作者信息

Zhang Hua, Liu Lian, Li Xin, Busayavalasa Kiran, Shen Yan, Hovatta Outi, Gustafsson Jan-Åke, Liu Kui

机构信息

Department of Chemistry and Molecular Biology, University of Gothenburg, SE-405 30 Gothenburg, Sweden;

Cancer Center, Qilu Hospital of Shandong University, 250012 Shandong, China;

出版信息

Proc Natl Acad Sci U S A. 2014 Dec 16;111(50):17983-8. doi: 10.1073/pnas.1421047111. Epub 2014 Dec 1.

Abstract

Whether or not oocyte regeneration occurs in adult life has been the subject of much debate. In this study, we have traced germ-cell lineages over the life spans of three genetically modified mouse models and provide direct evidence that oogenesis does not originate from any germline stem cells (GSCs) in adult mice. By selective ablation of all existing oocytes in a Gdf9-Cre;iDTR mouse model, we have demonstrated that no new germ cells were ever regenerated under pathological conditions. By in vivo tracing of oocytes and follicles in the Sohlh1-CreER(T2);R26R and Foxl2-CreER(T2);mT/mG mouse models, respectively, we have shown that the initial pool of oocytes is the only source of germ cells throughout the life span of the mice and that no adult oogenesis ever occurs under physiological conditions. Our findings clearly show that there are no GSCs that contribute to adult oogenesis in mice and that the initial pool of oocytes formed in early life is the only source of germ cells throughout the entire reproductive life span.

摘要

成年期是否会发生卵母细胞再生一直是备受争议的话题。在本研究中,我们追踪了三种基因改造小鼠模型整个生命周期中的生殖细胞谱系,并提供了直接证据,证明成年小鼠的卵子发生并非源自任何生殖系干细胞(GSC)。通过在Gdf9-Cre;iDTR小鼠模型中选择性消融所有现存的卵母细胞,我们证明在病理条件下不会有新的生殖细胞再生。分别通过在Sohlh1-CreER(T2);R26R和Foxl2-CreER(T2);mT/mG小鼠模型中对卵母细胞和卵泡进行体内追踪,我们表明,卵母细胞的初始库是小鼠整个生命周期中生殖细胞的唯一来源,并且在生理条件下不会发生成年期卵子发生。我们的研究结果清楚地表明,在小鼠中不存在对成年期卵子发生有贡献的生殖系干细胞,并且生命早期形成的卵母细胞初始库是整个生殖生命周期中生殖细胞的唯一来源。

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