Center of Excellence in Reproductive Sciences, Department of Clinical Sciences, College of Health Sciences, University of Kentucky, Lexington, Kentucky 40536, USA.
Endocrinology. 2010 Sep;151(9):4551-9. doi: 10.1210/en.2009-1444. Epub 2010 Jun 30.
Ovulation is preceded by intraovarian inflammatory reactions that occur in response to the preovulatory gonadotropin surge. As a main inflammatory event, leukocytes infiltrate the ovary and release proteolytic enzymes that degrade the extracellular matrix weakening the follicular wall, a required step for follicle rupture. This study aimed to quantitatively measure the infiltrating leukocytes, determine their cell types, and localize infiltration sites in the periovulatory rat ovary. Cycling adult and gonadotropin-stimulated immature rats were used as animal models. Ovaries were collected at five different stages of estrous cycle in the adult rats (diestrus, 1700 h; proestrus, 1500 h; proestrus, 2400 h; estrus, 0600 h; and metestrus, 1700 h) and at five different time points after superovulation induction in the immature rats (pregnant mare's serum gonadotrophin, 0 h; pregnant mare's serum gonadotrophin, 48 h; human chorionic gonadotropin, 6 h; human chorionic gonadotropin, 12 h; and human chorionic gonadotropin, 24 h). The ovaries were either dissociated into a single cell suspension for flow cytometric analysis or fixed for immunohistochemical localization of the leukocytes. Similar numbers of leukocytes were seen throughout the estrous cycle (approximately 500,000/ovary), except proestrus 2400 when 2-fold higher numbers of leukocytes were found (approximately 1.1 million/ovary). A similar trend of periovulatory rise of leukocyte numbers was seen in the superovulation-induced immature rat model, recapitulating a dramatic increase in leukocyte numbers upon gonadotropin stimulation. Both macrophage/granulocytes and lymphocytes were among the infiltrating leukocytes and were localized in the theca and interstitial tissues, where platelet-endothelial cell adhesion molecule-1 and intercellular adhesion molecule-1 may play roles in the transmigration of leukocytes, because their expressions correlates spatiotemporally with the infiltrating leukocytes. In addition, a strong inverse relationship between leukocyte numbers in the ovary and spleen, as well as significant reduction of leukocyte infiltration in the splenectomized rats, were seen, indicating that the spleen may serve as an immediate supplier of leukocytes to the periovulatory ovary.
排卵前,卵巢内会发生炎症反应,以响应促性腺激素的激增。作为主要的炎症事件,白细胞浸润卵巢并释放蛋白水解酶,降解细胞外基质,削弱卵泡壁,这是卵泡破裂所必需的步骤。本研究旨在定量测量浸润的白细胞,确定其细胞类型,并定位发情周期大鼠卵巢中的浸润部位。使用成年和促性腺激素刺激的未成熟大鼠作为动物模型。在成年大鼠的发情周期的五个不同阶段(发情前期,1700 h;发情前期,1500 h;发情前期,2400 h;发情期,0600 h;发情后期,1700 h)和在未成熟大鼠的超数排卵诱导后的五个不同时间点(孕马血清促性腺激素,0 h;孕马血清促性腺激素,48 h;人绒毛膜促性腺激素,6 h;人绒毛膜促性腺激素,12 h;人绒毛膜促性腺激素,24 h)收集卵巢。将卵巢分离成单个细胞悬浮液进行流式细胞术分析,或固定用于白细胞的免疫组织化学定位。在发情周期中,白细胞的数量相似(每个卵巢约 50 万个),但发情前期 2400 时发现白细胞数量增加了两倍(每个卵巢约 110 万个)。在超数排卵诱导的未成熟大鼠模型中也观察到了类似的排卵前白细胞数量增加的趋势,这反映了促性腺激素刺激后白细胞数量的急剧增加。浸润的白细胞包括巨噬细胞/粒细胞和淋巴细胞,并定位于卵巢的外膜和间质组织中,其中血小板内皮细胞黏附分子-1 和细胞间黏附分子-1可能在白细胞的迁移中起作用,因为它们的表达与浸润的白细胞具有时空相关性。此外,在卵巢和脾脏中的白细胞数量之间存在强烈的负相关关系,并且在脾切除大鼠中观察到白细胞浸润的显著减少,表明脾脏可能作为发情期卵巢的白细胞的即时供应源。