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体外培养的减数分裂前胎儿小鼠生殖细胞可形成典型的卵母细胞样细胞,但不会经历减数分裂。

Premeiotic fetal murine germ cells cultured in vitro form typical oocyte-like cells but do not progress through meiosis.

作者信息

Dong H S, Li L, Song Z H, Tang J, Xu B, Zhai X W, Sun L L, Zhang P, Li Z B, Pan Q J, Shi Q H, Shen W

机构信息

Laboratory of Germ Cell Biology, Institute of Animal Reproduction Development and Genetic Engineering, College of Animal Science and Technology, Qingdao Agricultural University, Qingdao, Shandong, China.

出版信息

Theriogenology. 2009 Jul 15;72(2):219-31. doi: 10.1016/j.theriogenology.2009.02.021. Epub 2009 Apr 9.

Abstract

A convenient method for fetal murine premeiotic germ cells to develop into oocytes in vitro has been established. Fetal ovaries from mice, collected 12.5 d postcoitus (dpc), were organ-cultured in vitro using a medium for organ growth, and the developmental potential regarding oocyte formation was determined. After 28 d of culture, premeiotic female germ cells developed into oocytes with a mean (+/-SD) diameter of 73.3+/-7.7 microm. However, follicles developed in vitro versus in vivo had fewer granulosa cells (32+/-2.6 vs. 142+/-9.5, respectively; P<0.01), and the ovaries had less mRNA for Cx37 and Cx43 (P<0.01). Oocytes in the first meiotic division phase were isolated from cultured ovaries or after hormone treatments. After exposure to okadaic acid at a final concentration of 1 microM, oocytes derived from premeiotic fetal female germ cells were able to undergo germinal vesicle breakdown but failed to complete the first meiotic division. Furthermore, the intracellular content of GSH in oocytes cultured in vitro was lower than that of oocytes matured in vivo (P<0.01). In conclusion, premeiotic germ cells derived from murine fetuses as early as 12.5 dpc were able to differentiate into germinal vesicle-stage oocytes but were unable to complete meiosis I in vitro.

摘要

已建立一种方便的方法,可使胎鼠减数分裂前生殖细胞在体外发育为卵母细胞。收集交配后12.5天(dpc)的小鼠胎儿卵巢,使用器官生长培养基进行体外器官培养,并确定其形成卵母细胞的发育潜能。培养28天后,减数分裂前的雌性生殖细胞发育为卵母细胞,平均(±标准差)直径为73.3±7.7微米。然而,体外发育的卵泡与体内发育的卵泡相比,颗粒细胞较少(分别为32±2.6个与142±9.5个;P<0.01),且卵巢中Cx37和Cx43的mRNA较少(P<0.01)。从培养的卵巢或激素处理后分离出处于第一次减数分裂期的卵母细胞。在终浓度为1 microM的冈田酸作用下,源自减数分裂前胎儿雌性生殖细胞的卵母细胞能够发生生发泡破裂,但未能完成第一次减数分裂。此外,体外培养的卵母细胞中谷胱甘肽的细胞内含量低于体内成熟的卵母细胞(P<0.01)。总之,早在12.5 dpc的鼠胎儿来源的减数分裂前生殖细胞能够分化为生发泡期卵母细胞,但在体外无法完成减数分裂I。

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