Zachos Nicholas C, Billiar Reinhart B, Albrecht Eugene D, Pepe Gerald J
Department of Physiological Sciences, Eastern Virginia Medical School, P.O. Box 1980, Norfolk, VA 23501-1980, USA.
Endocrinology. 2004 Feb;145(2):959-66. doi: 10.1210/en.2003-1078. Epub 2003 Oct 30.
We recently showed that the number of primordial follicles was reduced by 50% in ovaries of near-term fetal baboons deprived of estrogen in utero and restored to normal in animals supplemented with estrogen. Oocytes are avascular and rely on surrounding granulosa cells for nutrients, a process facilitated by microvilli on the oocyte surface. However, our understanding of oocyte microvillus development in the primate fetal ovary is incomplete. Thus, we determined whether estrogen regulates formation of oocyte microvilli in utero. Fetal ovaries were obtained on d 165 gestation (term = d 184) from baboons untreated (n = 3) or treated on d 100-165 with aromatase inhibitor CGS 20267 (estrogen suppressed by 95%; n = 5) or CGS 20267 and estradiol (n = 4). Follicles with intact (homogeneous cytoplasm) or nonintact (cytoplasm vacuolated) oocytes were quantified and the number/height of oocyte microvilli determined by electron microscopy. In untreated baboons, the mean (+/-se) number of follicles/0.08 mm(2) with an intact oocyte (11.5 +/- 0.5) was decreased (P < 0.05) by 70% in fetal ovaries of estrogen-suppressed baboons (3.4 +/- 0.2) and restored (P < 0.05) by CGS 20267 and estradiol (11.2 +/- 1.2). In estrogen-deprived fetuses, the number of microvilli/intact oocyte (23 +/- 3) was 56% lower (P < 0.01) than normal (52 +/- 5) and restored by CGS 20267 and estrogen (62 +/- 4). Moreover, in intact oocytes of estrogen-suppressed baboons, height (nm) of microvilli (105 +/- 11) was 54-62% lower (P < 0.01) than in intact oocytes of fetal ovaries of untreated (228 +/- 13) or estrogen-treated (274 +/- 17) baboons. In estrogen-replete baboons, the number of microvilli in intact oocytes was 2-fold greater (P < 0.01) than in nonintact oocytes. However, in estrogen-deprived baboons, no microvilli were detected in nonintact oocytes and the number of microvilli in intact oocytes was similar to that in nonintact oocytes of untreated fetuses. We conclude that development of microvilli in oocytes of primordial follicles in the primate fetal ovary is regulated by estrogen. Collectively, these results and those of our previous studies indicate that estrogen regulates fetal ovarian folliculogenesis and development of follicles with oocytes composed of microvilli critical for nutrient uptake and presumably long-term survival.
我们最近发现,在子宫内缺乏雌激素的近足月胎儿狒狒的卵巢中,原始卵泡数量减少了50%,而在补充雌激素的动物中则恢复正常。卵母细胞无血管,依靠周围的颗粒细胞提供营养,这一过程由卵母细胞表面的微绒毛促进。然而,我们对灵长类胎儿卵巢中卵母细胞微绒毛发育的了解并不完整。因此,我们确定雌激素是否在子宫内调节卵母细胞微绒毛的形成。在妊娠第165天(足月为第184天)从未经处理的狒狒(n = 3)或在第100 - 165天用芳香化酶抑制剂CGS 20267处理的狒狒(雌激素抑制95%;n = 5)或CGS 20267和雌二醇处理的狒狒(n = 4)获取胎儿卵巢。对具有完整(均匀细胞质)或不完整(细胞质空泡化)卵母细胞的卵泡进行定量,并通过电子显微镜确定卵母细胞微绒毛的数量/高度。在未经处理的狒狒中,每0.08 mm²具有完整卵母细胞的卵泡平均数量(+/-标准误)为(11.5 +/- 0.5),在雌激素抑制的狒狒胎儿卵巢中减少了70%(P < 0.05)(3.4 +/- 0.2),并通过CGS 20267和雌二醇恢复(P < 0.05)(11.2 +/- 1.2)。在缺乏雌激素的胎儿中,每个完整卵母细胞的微绒毛数量(23 +/- 3)比正常情况低56%(P < 0.01)(52 +/- 5),并通过CGS 20267和雌激素恢复(62 +/- 4)。此外,在雌激素抑制的狒狒的完整卵母细胞中,微绒毛的高度(nm)(105 +/- 11)比未经处理(228 +/- 13)或雌激素处理(274 +/- 17)的狒狒胎儿卵巢的完整卵母细胞低54 - 62%(P < 0.01)。在雌激素充足的狒狒中,完整卵母细胞中的微绒毛数量比不完整卵母细胞多2倍(P < 0.01)。然而,在缺乏雌激素的狒狒中,在不完整卵母细胞中未检测到微绒毛,并且完整卵母细胞中的微绒毛数量与未经处理胎儿的不完整卵母细胞中的微绒毛数量相似。我们得出结论,灵长类胎儿卵巢中原始卵泡卵母细胞微绒毛的发育受雌激素调节。总体而言,这些结果以及我们先前研究的结果表明,雌激素调节胎儿卵巢卵泡发生以及具有由对营养摄取和可能的长期存活至关重要的微绒毛组成的卵母细胞的卵泡发育。