Bao B, Garverick H A, Smith G W, Smith M F, Salfen B E, Youngquist R S
Department of Animal Sciences, University of Missouri-Columbia, 65211, USA.
Biol Reprod. 1997 Jun;56(6):1466-73. doi: 10.1095/biolreprod56.6.1466.
The objective of the present study was to examine changes in expression of mRNA encoding 3beta-hydroxysteroid dehydrogenase delta4,delta5 isomerase (3beta-HSD) during recruitment and selection of bovine ovarian follicles. Dairy heifers (4-5/time period) were ovariectomized at 12, 24, 36, 48, 60, 72, 84, or 96 h after initiation of the first follicular wave (Time 0) following estrus. Expression of 3beta-HSD mRNA was localized by in situ hybridization and quantified by image analysis. Expression of 3beta-HSD mRNA was first detected in theca interna cells of preantral follicles with a well-developed theca layer and in granulosa cells of follicles > or = 8 mm in diameter. Regardless of stage of follicular wave, expression of 3beta-HSD mRNA in granulosa cells of follicles > or = 8 mm was correlated with follicular size (r = 0.665; p < 0.01). The 36-h time period appeared to be a transition period for selection since dominant follicles were detected by size and expression of 3beta-HSD mRNA in some cows but not in others. By 48 h after wave initiation, dominant follicles could be identified by both size and expression of 3beta-HSD mRNA. Expression of mRNA for 3beta-HSD in theca cells was higher (p < 0.05) at 24 h than at 12 h and remained elevated thereafter through 96 h. In contrast to theca cells, expression of mRNA for 3beta-HSD was undetectable within granulosa cells at 12 and 24 h. At 36 h, 3beta-HSD mRNA was expressed in granulosa cells of healthy follicles > or = 8 mm, and expression was higher (p < 0.05) at 48 h compared with 36 h. Expression of 3beta-HSD mRNA levels increased further in granulosa cells (p < 0.05) at 84 and 96 h compared to 48 h. Upon detection of mRNA for 3beta-HSD in granulosa cells, high levels of expression were always found in one (dominant) follicle/cow with the exception of two cows at 36 and 84 h that expressed 3beta-HSD mRNA in two large healthy follicles. Expression of 3beta-HSD mRNA was also detectable in granulosa cells of a few large atretic follicles in which remnant granulosa cells appeared to be luteinized. Healthy follicles expressed higher (p < 0.05) levels of 3beta-HSD mRNA in both theca and granulosa cells than did atretic follicles. Expression of 3beta-HSD mRNA in theca cells was higher (p < 0.01) in dominant follicles than in other subordinate healthy follicles. These results indicate that only selected dominant follicles express 3beta-HSD mRNA within granulosa cells, and expression increased in both thecal and granulosa cells during the follicular wave. Therefore, expression of 3beta-HSD mRNA within granulosa cells may be associated with the mechanism of selection of the dominant follicle during a follicular wave and may be required for maximum steroid production during follicular dominance.
本研究的目的是检测在牛卵巢卵泡募集和选择过程中,编码3β-羟基类固醇脱氢酶δ4,δ5异构酶(3β-HSD)的mRNA表达变化。在发情后第一个卵泡波开始(时间0)后的12、24、36、48、60、72、84或96小时,对奶牛小母牛(每个时间段4 - 5头)进行卵巢切除。通过原位杂交定位3β-HSD mRNA的表达,并通过图像分析进行定量。3β-HSD mRNA的表达首先在具有发育良好的卵泡膜层的窦前卵泡的卵泡膜内层细胞以及直径≥8 mm的卵泡的颗粒细胞中检测到。无论卵泡波处于哪个阶段,直径≥8 mm的卵泡颗粒细胞中3β-HSD mRNA的表达与卵泡大小相关(r = 0.665;p < 0.01)。36小时这个时间段似乎是一个选择的过渡期,因为在一些奶牛中可以通过大小和3β-HSD mRNA的表达检测到优势卵泡,但在其他奶牛中则检测不到。到卵泡波开始后48小时,可以通过大小和3β-HSD mRNA的表达来识别优势卵泡。卵泡膜细胞中3β-HSD mRNA的表达在24小时时高于12小时(p < 0.05),此后一直升高至96小时。与卵泡膜细胞相反,在12和24小时时,颗粒细胞内未检测到3β-HSD mRNA的表达。在36小时时,直径≥8 mm的健康卵泡的颗粒细胞中表达3β-HSD mRNA,与36小时相比,48小时时表达更高(p < 0.05)。与48小时相比,84和96小时时颗粒细胞中3β-HSD mRNA水平进一步升高(p < 0.05)。在颗粒细胞中检测到3β-HSD mRNA后,除了在36和84小时时有两头奶牛在两个大的健康卵泡中表达3β-HSD mRNA外,在每头奶牛的一个(优势)卵泡中总是发现高水平的表达。在一些大的闭锁卵泡的颗粒细胞中也可检测到3β-HSD mRNA的表达,其中残留的颗粒细胞似乎已黄体化。健康卵泡在卵泡膜和颗粒细胞中表达的3β-HSD mRNA水平均高于闭锁卵泡(p < 0.05)。优势卵泡中卵泡膜细胞中3β-HSD mRNA的表达高于其他次级健康卵泡(p < 0.01)。这些结果表明,只有被选择的优势卵泡在颗粒细胞中表达3β-HSD mRNA,并且在卵泡波期间卵泡膜和颗粒细胞中的表达均增加。因此,颗粒细胞中3β-HSD mRNA的表达可能与卵泡波期间优势卵泡的选择机制有关,并且可能是卵泡优势期最大类固醇产生所必需的。