Takao Y, Honda T, Ueda M, Hattori N, Yamada S, Maeda M, Fujiwara H, Mori T, Wimalasena J
Department of Gynecology and Obstetrics, Faculty of Medicine, Kyoto University, Sakyo-ku, Japan.
Mol Hum Reprod. 1997 Jul;3(7):569-78. doi: 10.1093/molehr/3.7.569.
We examined the immunohistochemical localization of luteinizing hormone (LH)/human chorionic gonadotrophin (HCG) receptor (LH-R) in the human ovary using the anti-human LH-R monoclonal antibody, 3B5. In the antral follicles, LH-R was detected on theca interna cells. In pre-ovulatory follicles, granulosa cells also expressed LH-R. During corpus luteum formation, granulosa cells seemed to increase the expression of LH-R, and in corpus luteum of mid-luteal phase, large luteal cells expressed LH-R more intensely than small luteal cells. In the regressing corpus luteum, LH-R was almost undetectable on both luteal cells, whereas in the corpus luteum of early pregnancy, LH-R continued to be expressed on large luteal cells. The granulosa cells obtained from the patients undergoing in-vitro fertilization therapy were cultured for 3 days in serum-free medium, without or with HCG (10 IU/ml) and tumour necrosis factor (TNF)alpha (10 ng/ml). Flow cytometry showed that the expression of LH-R on the cell surface of luteinizing granulosa cells was enhanced by HCG, but was unaffected by TNFalpha. These results suggest that the main target cells for LH/HCG change from theca interna cells/small luteal cells to granulosa cells/large luteal cells during ovulation, corpus luteum formation, and differentiation into the corpus luteum of pregnancy, probably under the influence of LH/HCG.
我们使用抗人促黄体生成素受体(LH-R)单克隆抗体3B5,检测了人卵巢中促黄体生成素(LH)/人绒毛膜促性腺激素(HCG)受体(LH-R)的免疫组化定位。在窦状卵泡中,在卵泡内膜细胞上检测到LH-R。在排卵前卵泡中,颗粒细胞也表达LH-R。在黄体形成过程中,颗粒细胞似乎增加了LH-R的表达,并且在黄体中期的黄体中,大黄体细胞比小黄体细胞更强烈地表达LH-R。在退化的黄体中,两种黄体细胞上几乎检测不到LH-R,而在妊娠早期的黄体中,大黄体细胞上继续表达LH-R。从接受体外受精治疗的患者获得的颗粒细胞在无血清培养基中培养3天,添加或不添加HCG(10 IU/ml)和肿瘤坏死因子(TNF)α(10 ng/ml)。流式细胞术显示,HCG增强了促黄体生成颗粒细胞表面LH-R的表达,但不受TNFα的影响。这些结果表明,在排卵、黄体形成以及分化为妊娠黄体的过程中,LH/HCG的主要靶细胞可能在LH/HCG的影响下,从卵泡内膜细胞/小黄体细胞转变为颗粒细胞/大黄体细胞。