Grazul-Bilska Anna T, Navanukraw Chainarong, Johnson Mary Lynn, Arnold Daniel A, Reynolds Lawrence P, Redmer Dale A
Department of Animal and Range Sciences, North Dakota State University, Fargo, North Dakota 58105-5727, USA.
Reproduction. 2006 Oct;132(4):579-87. doi: 10.1530/REP-06-0009.
This study was conducted to evaluate the expression of endothelial nitric oxide synthase (eNOS) in ovarian follicles and corpora lutea (CL) throughout the estrous cycle in sheep. Three experiments were conducted to (1) immunolocalize eNOS protein, (2) determine expression of mRNA for eNOS and its receptor guanylate cyclase 1 soluble beta3 (GUCY1B3), and (3) co-localize eNOS and vascular endothelial growth factor (VEGF) proteins in the follicles and/or CL throughout the estrous cycle. In experiment 1, ovaries were collected from ewes treated with FSH, to induce follicular growth or atresia. In experiment 2, ovaries were collected from ewes treated with FSH and hCG to induce follicular growth and ovulation. In experiment 3, ovaries were collected from superovulated ewes to generate multiple CL on days 2, 4, 10, and 15 of the estrous cycle. In experiments 1 and 2, the expression of eNOS protein was detected in the blood vessels of the theca externa and interna of healthy ovarian follicles. However, in early and advanced atretic follicles, eNOS protein expression was absent or reduced. During the immediate postovulatory period, eNOS protein expression was detected in thecal-derived cells that appeared to be invading the granulosa layer. Expression of eNOS mRNA tended to increase in granulosa cells at 12 and 24 h, and in theca cells 48 h after hCG injection. In experiment 3, eNOS protein was located in the blood vessels of the CL during the estrous cycle. Dual localization of eNOS and VEGF proteins in the CL demonstrated that both were found in the blood vessels.
本研究旨在评估绵羊发情周期中卵巢卵泡和黄体(CL)中内皮型一氧化氮合酶(eNOS)的表达。进行了三项实验,以(1)免疫定位eNOS蛋白,(2)测定eNOS及其受体鸟苷酸环化酶1可溶性β3(GUCY1B3)的mRNA表达,以及(3)在发情周期的卵泡和/或黄体中对eNOS和血管内皮生长因子(VEGF)蛋白进行共定位。在实验1中,从用促卵泡素(FSH)处理以诱导卵泡生长或闭锁的母羊采集卵巢。在实验2中,从用FSH和人绒毛膜促性腺激素(hCG)处理以诱导卵泡生长和排卵的母羊采集卵巢。在实验3中,从超排母羊采集卵巢,以在发情周期的第2、4、10和15天生成多个黄体。在实验1和2中,在健康卵巢卵泡的外膜和内膜血管中检测到eNOS蛋白的表达。然而,在早期和晚期闭锁卵泡中,eNOS蛋白表达缺失或减少。在排卵后即刻,在似乎侵入颗粒层的膜来源细胞中检测到eNOS蛋白表达。hCG注射后12和24小时,颗粒细胞中eNOS mRNA表达趋于增加,48小时后在膜细胞中表达增加。在实验3中,发情周期期间eNOS蛋白位于黄体的血管中。黄体中eNOS和VEGF蛋白的双重定位表明两者都存在于血管中。