Molecular Endocrinology Laboratory, Animal Biochemistry Division, National Dairy Research Institute, Haryana, India.
Domest Anim Endocrinol. 2011 Nov;41(4):195-206. doi: 10.1016/j.domaniend.2011.07.001. Epub 2011 Aug 25.
In the present study, buffalo granulosa cells were cultured under serum-free conditions and characterized to study the changes in gene expression associated with the transition of granulosa cells from estrogen- to progesterone-secreting phenotype. The cells were cultured in vitro under completely serum-free conditions for 8 d. Gene expression and hormone analysis showed that on day 4 granulosa cells exhibit FSH responsiveness with preovulatory phenotype having highest CYP19 gene expression and 17β-estradiol production, whereas a significant increase in transcript abundance of STAR, CYP11, and HSD3B genes accompanied with an increase in progesterone production was observed on day 8. Cells treated with LH on day 4 followed by gene expression analysis at 1, 2, 4, 6, 18, and 24 h showed significant increase in transcripts of LH-responsive genes. In conclusion, culture condition used in the present study showed that granulosa cells were FSH responsive and attained attributes of granulosa cells of dominant follicles at day 4 with highest CYP19 and LHR gene expression beyond which they acquired the ability to luteinize and thus were more LH responsive. In addition, after LH treatment, analysis of early LH-responsive genes (EGR2, RUNX1, and NR4A1) on day 4 showed that granulosa cells at this stage in culture exhibits phenotype similar to that of preovulatory follicles before LH surge in vivo and corresponds to the in vivo transition of well-orchestrated gene expression profile after LH surge. The characterized culture conditions represent a suitable in vitro model for analysis of genes involved in terminal differentiation of granulosa cells from FSH- to LH-responsive phenotype during folliculogenesis in buffalo.
在本研究中,我们在无血清条件下培养水牛颗粒细胞,并对其进行了特征分析,以研究与颗粒细胞从雌激素分泌表型向孕激素分泌表型转变相关的基因表达变化。我们将细胞在完全无血清条件下培养 8 天。基因表达和激素分析表明,在第 4 天,颗粒细胞表现出对 FSH 的反应性,具有促排卵表型,CYP19 基因表达和 17β-雌二醇产生最高,而在第 8 天,STAR、CYP11 和 HSD3B 基因的转录丰度显著增加,同时孕激素产量增加。第 4 天用 LH 处理细胞,然后在 1、2、4、6、18 和 24 h 进行基因表达分析,显示 LH 反应基因的转录显著增加。总之,本研究中使用的培养条件表明,颗粒细胞对 FSH 有反应性,并在第 4 天获得优势卵泡颗粒细胞的特征,CYP19 和 LHR 基因表达最高,此后它们获得了黄体化的能力,因此对 LH 的反应性更强。此外,在第 4 天用 LH 处理后,分析早期 LH 反应基因(EGR2、RUNX1 和 NR4A1)表明,在培养的这个阶段,颗粒细胞表现出与体内 LH 激增前促排卵卵泡相似的表型,与体内 LH 激增后协调良好的基因表达谱的转变相对应。所鉴定的培养条件代表了一种合适的体外模型,可用于分析水牛卵泡发生过程中颗粒细胞从 FSH 反应表型向 LH 反应表型的终末分化过程中涉及的基因。