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由减数分裂前胎儿生殖细胞衍生的小鼠卵母细胞产生的活体后代。

Live offspring produced by mouse oocytes derived from premeiotic fetal germ cells.

作者信息

Shen Wei, Zhang Donghui, Qing Tingting, Cheng Jing, Bai Zhaodai, Shi Yuqiang, Ding Mingxiao, Deng Hongkui

机构信息

College of Life Sciences, Peking University, Beijing 100871, China.

出版信息

Biol Reprod. 2006 Oct;75(4):615-23. doi: 10.1095/biolreprod.106.051482. Epub 2006 May 24.

Abstract

Mature mouse oocytes currently can be generated in vitro from the primary oocytes of primordial follicles but not from premeiotic fetal germ cells. In this study we established a simple, efficient method that can be used to obtain mature oocytes from the premeiotic germ cells of a fetal mouse 12.5 days postcoitum (dpc). Mouse 12.5-dpc fetal ovaries were transplanted under the kidney capsule of recipient mice to initiate oocyte growth from the premeiotic germ cell stage, and they were recovered after 14 days. Subsequently, the primary and early secondary follicles generated in the ovarian grafts were isolated and cultured for 16 days in vitro. The mature oocytes ovulated from these follicles were able to fertilize in vitro to produce live offspring. We further show that the in vitro fertilization offspring were normal and able to successfully mate with both females and males, and the patterns of the methylated sites of the in vitro mature oocytes were similar to those of normal mice. This is the first report describing premeiotic fetal germ cells able to enter a second meiosis and support embryonic development to term by a combination of in vivo transplantation and in vitro culture. In addition, we have shown that the whole process of oogenesis, from premeiotic germ cells to germinal vesicle (GV)-stage oocytes, can be carried out under the kidney capsule.

摘要

目前,成熟的小鼠卵母细胞可以从原始卵泡的初级卵母细胞体外生成,但不能从减数分裂前的胎儿生殖细胞生成。在本研究中,我们建立了一种简单、高效的方法,可用于从妊娠12.5天(dpc)的胎儿小鼠减数分裂前的生殖细胞中获得成熟卵母细胞。将12.5 dpc的小鼠胎儿卵巢移植到受体小鼠的肾被膜下,以使减数分裂前的生殖细胞阶段开始卵母细胞生长,并在14天后回收。随后,分离卵巢移植物中产生的初级和早期次级卵泡,并在体外培养16天。从这些卵泡中排卵的成熟卵母细胞能够在体外受精以产生活的后代。我们进一步表明,体外受精后代是正常的,并且能够成功地与雌性和雄性交配,并且体外成熟卵母细胞的甲基化位点模式与正常小鼠相似。这是第一份描述减数分裂前的胎儿生殖细胞能够通过体内移植和体外培养相结合进入第二次减数分裂并支持胚胎发育至足月的报告。此外我们还表明,从减数分裂前的生殖细胞到生发泡(GV)期卵母细胞的整个卵子发生过程都可以在肾被膜下进行。

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