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[小鼠体外培养卵母细胞中生长分化因子9基因的表达]

[Growth differentiation factor-9 gene expression in in vitro cultured oocytes in mice].

作者信息

Peng Yu-hong, Zhuang Guang-lun, Zhou Can-quan

机构信息

Department of Obstetrics and Gynecology, Wuhan General Hospital of Guangzhou Command, Wuhan 430070, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2006 Sep;26(9):1341-5.

Abstract

OBJECTIVE

To explore the relation between oocyte maturation and growth differentiation factor-9 (GDF-9) gene expression.

METHODS

Ovariectomy was performed in 50 Kunming female mice of 10 days old, and the preantral follicles were isolated from the ovaries and cultured in medium drops for 12 days. Oocytes and somatic cells were mechanically isolated. The oocytes cultured in vitro for 2, 4, 6, 8, 10, and 12 days constituted the in vitro cultured group and the oocytes obtained from female mice of 12, 14, 16, 18, 20, and 22 days old served as the in vivo group. Semi-quantitative RT-PCR and agar gel electrophoresis were performed to quantify GDF-9 gene expression in each oocyte.

RESULTS

Follicle survival, antrum formation and maturation rate was 89.5%, 51.8% and 56.6% in the in vitro cultured follicles, respectively. GDF-9 gene expression on days 2, 4, 6, 8, 10, and 12 in in vitro cultured oocytes was 0.83-/+0.08, 0.52-/+0.09, 0.45-/+0.13, 0.49-/+0.09, 0.49-/+0.09, and 0.68-/+0.08, respectively; GDF-9 gene expression in in vivo grown oocytes of 12, 14, 16, 18, 20, and 22 days were 0.64-/+0.35, 0.48-/+0.10, 0.52-/+0.10, 0.66-/+0.08, 0.72-/+0.09, and 0.91-/+0.11, respectively. Between days 8 and 12, GDF-9 gene expression in in vitro cultured oocyte was significantly lower than that in in vivo grown oocytes (P<0.05).

CONCLUSION

MII oocytes can be obtained from in vitro culture of the preantral follicles. GDF-9 gene expression in the oocytes varies with their growth stages. Between days 8 and 12 of in vitro culture, GDF-9 gene expression in the cultured oocytes is different from that in in vivo grown oocytes.

摘要

目的

探讨卵母细胞成熟与生长分化因子9(GDF - 9)基因表达之间的关系。

方法

对50只10日龄的昆明雌性小鼠进行卵巢切除术,从卵巢中分离出窦前卵泡并在培养液滴中培养12天。通过机械方法分离卵母细胞和体细胞。体外培养2、4、6、8、10和12天的卵母细胞构成体外培养组,取自12、14、16、18、20和22日龄雌性小鼠的卵母细胞作为体内组。采用半定量逆转录聚合酶链反应(RT - PCR)和琼脂糖凝胶电泳对每个卵母细胞中的GDF - 9基因表达进行定量分析。

结果

体外培养卵泡的卵泡存活率、腔形成率和成熟率分别为89.5%、51.8%和56.6%。体外培养卵母细胞在第2、4、6、8、10和12天的GDF - 9基因表达分别为0.83±0.08、0.52±0.09、0.45±0.13、0.49±0.09、0.49±0.09和0.68±0.08;体内生长的12、14、16、18、20和22日龄卵母细胞的GDF - 9基因表达分别为0.64±0.35、0.48±0.10、0.52±0.10、0.66±0.08、0.72±0.09和0.91±0.11。在第8天至12天之间,体外培养卵母细胞中的GDF - 9基因表达显著低于体内生长的卵母细胞(P < 0.05)。

结论

可通过体外培养窦前卵泡获得MII期卵母细胞。卵母细胞中GDF - 9基因表达随其生长阶段而变化。在体外培养的第8天至12天之间,培养卵母细胞中的GDF - 9基因表达与体内生长的卵母细胞不同。

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