Prochazka Radek, Nemcova Lucie, Nagyova Eva, Kanka Jiri
Institute of Animal Physiology and Genetics, Academy of Sciences of the Czech Republic, 277 21 Libechov, Czech Republic.
Biol Reprod. 2004 Oct;71(4):1290-5. doi: 10.1095/biolreprod.104.027912. Epub 2004 Jun 9.
We have shown previously that porcine cumulus and mural granulosa cells produce a factor that is very similar, if not identical, to the oocyte-derived cumulus expansion-enabling factor (CEEF). Because growth differentiation factor 9 (GDF9) is the most likely candidate for the CEEF, in the present study we tested the hypothesis that GDF9 is expressed not only in oocytes in the pig but also in somatic follicular cells. In addition, we asked whether the relative abundance (RA) of GDF9 mRNA changes in oocytes and/or follicular cells during the periovulatory period or culture of oocyte-cumulus complexes (OCCs) in vitro. Denuded oocytes, OCCs, cumulus, and mural granulosa cells were isolated from growing and preovulatory follicles. Total RNA was extracted from the cells, and reverse transcription-polymerase chain reaction (RT-PCR) was carried out using specific oligonucleotide primers. The RT-PCR resulted in amplification of a product of expected size (277 base pairs) in samples prepared from all follicular cell types. The identity of the RT-PCR products with GDF9 was confirmed by analysis of their nucleotide sequence, which was 88% and 91% identical to human and ovine GDF9, respectively. The RA of GDF9 mRNA in the somatic follicular cells was approximately fourfold lower than in oocytes. Assessment of the RA of GDF9 mRNA during the periovulatory period and during culture and expansion of OCCs in vitro revealed that it remained stable in oocytes and mural granulosa cells and decreased significantly in expanding cumulus cells. We conclude that GDF9 mRNA can be produced by somatic follicular cells in the pig and that cumulus expansion is not preceded or accompanied by an increase in the RA of GDF9 mRNA in any of the tested cell types.
我们之前已经表明,猪的卵丘细胞和壁层颗粒细胞产生一种因子,该因子即便与卵母细胞衍生的卵丘扩展促进因子(CEEF)不完全相同,也极为相似。由于生长分化因子9(GDF9)是CEEF最有可能的候选因子,在本研究中,我们检验了这样一个假设,即GDF9不仅在猪的卵母细胞中表达,也在卵泡体细胞中表达。此外,我们还探究了在排卵前期或卵母细胞-卵丘复合体(OCC)体外培养期间,卵母细胞和/或卵泡细胞中GDF9 mRNA的相对丰度(RA)是否会发生变化。从生长卵泡和排卵前卵泡中分离出裸卵、OCC、卵丘细胞和壁层颗粒细胞。从这些细胞中提取总RNA,并使用特异性寡核苷酸引物进行逆转录-聚合酶链反应(RT-PCR)。RT-PCR在所有卵泡细胞类型制备的样本中均扩增出预期大小(277个碱基对)的产物。通过对其核苷酸序列进行分析,证实RT-PCR产物与GDF9一致,该序列分别与人类和绵羊GDF9的序列有88%和91%的同源性。卵泡体细胞中GDF9 mRNA的RA约比卵母细胞中的低四倍。对排卵前期以及OCC体外培养和扩展期间GDF9 mRNA的RA进行评估发现,其在卵母细胞和壁层颗粒细胞中保持稳定,而在扩展的卵丘细胞中显著降低。我们得出结论,猪的卵泡体细胞能够产生GDF9 mRNA,并且在任何测试细胞类型中,卵丘扩展之前或伴随过程中,GDF9 mRNA的RA均未增加。