Shen Wei, Li Lan, Bai Zhaodai, Pan Qingjie, Ding Mingxiao, Deng Hongkui
College of Animal Science and Technology, Institute of Animal Reproduction Development and Genetic Engineering, Qingdao Agricultural University, Qingdao 266109, China.
Reproduction. 2007 Aug;134(2):223-31. doi: 10.1530/REP-06-0378.
Little is known about the mechanisms underlying primordial follicular formation and the acquisition of competence to resume meiosis by growing oocytes. It is therefore important to establish an in vitro experimental model that allows one to study such mechanisms. Mouse follicular development has been studied in vitro over the past several years; however, no evidence has been presented showing that mature oocytes can be obtained from mouse fetal germ cells prior to the formation of primordial follicles. In this study, a method has been established to obtain mature oocytes from the mouse fetal germ cells at 16.5 days postcoitum (dpc). From the initiation of primordial follicular formation to the growth of early secondary follicles, ovarian tissues from 16.5 dpc fetal mice were cultured in vitro for 14 days. Subsequently, 678 intact secondary follicles were isolated from 182 mouse fetal ovaries and cultured for 12 days. A total of 141 oocytes inside antral follicles were matured in vitro, and 102 oocytes underwent germinal vesicle breakdown. We found that 97 oocytes were fertilized and 15 embryos were able to form morula-blastocysts. We also analyzed various genomic imprinting markers and showed that the erasure of genomic imprinting markers in the parental generation was also imposed on the oocytes that developed from fetal germ cells. Our results demonstrate that mouse fetal germ cells are able to form primordial follicles with ovarian cells, and that oocytes within the growing follicles are able to mature normally in vitro.
关于原始卵泡形成以及生长中的卵母细胞恢复减数分裂能力的潜在机制,我们所知甚少。因此,建立一个体外实验模型来研究这些机制非常重要。在过去几年中,小鼠卵泡发育已在体外进行了研究;然而,尚无证据表明在原始卵泡形成之前能够从小鼠胎儿生殖细胞中获得成熟卵母细胞。在本研究中,已建立了一种方法,可在妊娠16.5天(dpc)从小鼠胎儿生殖细胞中获得成熟卵母细胞。从原始卵泡形成开始到早期次级卵泡生长阶段,将16.5 dpc胎儿小鼠的卵巢组织在体外培养14天。随后,从182个小鼠胎儿卵巢中分离出678个完整的次级卵泡,并培养12天。共有141个窦状卵泡内的卵母细胞在体外成熟,102个卵母细胞发生了生发泡破裂。我们发现97个卵母细胞受精,15个胚胎能够形成桑葚胚-囊胚。我们还分析了各种基因组印记标记,并表明亲代基因组印记标记的消除也施加于从胎儿生殖细胞发育而来的卵母细胞上。我们的结果表明,小鼠胎儿生殖细胞能够与卵巢细胞形成原始卵泡,并且生长卵泡内的卵母细胞能够在体外正常成熟。