Literature DB >> 19361852

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

H S Dong1, L Li, Z H Song, J Tang, B Xu, X W Zhai, L L Sun, P Zhang, Z B Li, Q J Pan, Q H Shi, W Shen.   

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.

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Year:  2009        PMID: 19361852     DOI: 10.1016/j.theriogenology.2009.02.021

Source DB:  PubMed          Journal:  Theriogenology        ISSN: 0093-691X            Impact factor:   2.740


  10 in total

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2.  Intravenous Administration of Human Umbilical Cord Mesenchymal Stem Cells Improves Cognitive Impairments and Reduces Amyloid-Beta Deposition in an AβPP/PS1 Transgenic Mouse Model.

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  10 in total

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