Bao B, Calder M D, Xie S, Smith M F, Salfen B E, Youngquist R S, Garverick H A
Departments of Animal Sciences, University of Missouri, Columbia, Missouri 65211, USA.
Biol Reprod. 1998 Oct;59(4):953-9. doi: 10.1095/biolreprod59.4.953.
Expression of mRNA encoding steroidogenic acute regulatory protein (StAR) in bovine follicles during recruitment and selection was examined. 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) after estrus. Follicles were collected and stored at -80 degrees C until sectioning. Expression of StAR mRNA was localized by in situ hybridization and quantified by image analysis. Expression of StAR mRNA was first detected in theca interna of antral follicles as small as 0.5 mm in diameter and increased with increasing follicular size (>/= 4 mm; r = 0.75; p < 0.001). StAR mRNA was undetectable in granulosa of healthy follicles at any size or stage of follicular wave examined. However, granulosa or luteinized granulosa of some advanced or late atretic follicles expressed StAR mRNA. During recruitment, StAR mRNA expression in theca cells was similar among recruited follicles (4-8 mm). During selection of dominant follicles (36-48 h), StAR mRNA was expressed in theca of more than one follicle (7-9 mm); therefore, expression of StAR mRNA may not be associated with dominant follicle selection. StAR mRNA in theca was higher (p < 0.05) at 48 h after initiation of the first follicular wave than at 12, 24, and 36 h, and it remained elevated thereafter through 96 h. Dominant follicles expressed more (p < 0.01) StAR mRNA in theca than did subordinate healthy follicles. Healthy follicles expressed higher (p < 0.05) StAR mRNA in theca than atretic follicles. In summary, levels of StAR mRNA increased in theca with stage of follicular wave and size of follicles. Follicular atresia was associated with reduced expression of StAR mRNA in theca cells. The results indicate that expression of StAR mRNA in theca may not be the primary limiting factor for follicular recruitment and selection.
研究了牛卵泡募集和选择过程中编码类固醇生成急性调节蛋白(StAR)的mRNA的表达。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。收集卵泡并储存在-80℃直至切片。通过原位杂交定位StAR mRNA的表达,并通过图像分析进行定量。StAR mRNA的表达首先在直径小至0.5mm的窦状卵泡的内膜中检测到,并随着卵泡大小增加(≥4mm;r = 0.75;p < 0.001)而增加。在所检查的卵泡波的任何大小或阶段,健康卵泡的颗粒细胞中均未检测到StAR mRNA。然而,一些晚期或闭锁卵泡的颗粒细胞或黄体化颗粒细胞表达StAR mRNA。在募集期间,募集卵泡(4 - 8mm)之间的内膜细胞中StAR mRNA表达相似。在优势卵泡选择期间(36 - 48小时),不止一个卵泡(7 - 9mm)的内膜中表达StAR mRNA;因此,StAR mRNA的表达可能与优势卵泡选择无关。第一个卵泡波开始后48小时,内膜中的StAR mRNA高于12、24和36小时(p < 0.05),此后一直升高至96小时。优势卵泡内膜中表达的StAR mRNA比从属健康卵泡更多(p < 0.01)。健康卵泡内膜中表达的StAR mRNA比闭锁卵泡更高(p < 0.05)。总之,StAR mRNA水平随着卵泡波阶段和卵泡大小而在内膜中增加。卵泡闭锁与内膜细胞中StAR mRNA表达降低有关。结果表明,内膜中StAR mRNA的表达可能不是卵泡募集和选择的主要限制因素。