Sakumoto Ryosuke, Shibaya Masami, Okuda Kiyoshi
Laboratory of Reproductive Endocrinology, Faculty of Agriculture, Okayama University, Japan.
J Reprod Dev. 2003 Dec;49(6):441-9. doi: 10.1262/jrd.49.441.
The aim of this study was to investigate whether functional tumor necrosis factor-alpha (TNFalpha) receptors are present in the granulosa cells and the cells of theca interna (theca cells), obtained from bovine follicles classified into one of three groups. Each group was defined as either small vesicular ovarian follicles (small follicles; 3-5 mm in diameter), preovulatory mature ovarian follicles (preovulatory follicles) or atretic follicles (12-18 mm) according to gross examination of the corpus luteum in the epsilateral or contralateral ovary and the uterus (size, color, consistency and mucus), and the ratio of progesterone (P(4)) and estradiol-17beta (E(2)) concentrations in follicular fluid. A Scatchard analysis showed the presence of a high-affinity binding site on both granulosa and theca cells from all follicles examined (dissociation constant: 4.7 +/- 0.15 to 6.9 +/- 1.40 nM). Moreover, TNFalpha receptor concentrations in granulosa and theca cells obtained from atretic follicles were significantly higher than those in the cells from preovulatory follicles (P<0.05). Exposure of cultured granulosa cells from small antral follicles to recombinant human TNFalpha (rhTNFalpha; 0.06-6 nM) inhibited E(2) secretion in a dose-dependent fashion (P<0.01), but did not affect P(4) secretion. In addition, rhTNFalpha inhibited follicle stimulating hormone-, forskolin- or dibutylyl cyclic AMP-induced P(4) and E(2) secretion by the cells (P<0.01). These results indicate the presence of functional TNFalpha receptors in bovine granulosa and theca cells in small, preovulatory and atretic follicles, and suggest that TNFalpha plays a role in regulating their secretory function.
本研究的目的是调查从分为三组之一的牛卵泡中获得的颗粒细胞和卵泡内膜细胞(卵泡膜细胞)中是否存在功能性肿瘤坏死因子-α(TNFα)受体。根据同侧或对侧卵巢和子宫中黄体的大体检查(大小、颜色、质地和黏液)以及卵泡液中孕酮(P4)和雌二醇-17β(E2)浓度的比值,每组分别定义为小泡状卵巢卵泡(小卵泡;直径3-5毫米)、排卵前成熟卵巢卵泡(排卵前卵泡)或闭锁卵泡(12-18毫米)。Scatchard分析显示,在所检查的所有卵泡的颗粒细胞和卵泡膜细胞上均存在高亲和力结合位点(解离常数:4.7±0.15至6.9±1.40 nM)。此外,从闭锁卵泡获得的颗粒细胞和卵泡膜细胞中的TNFα受体浓度显著高于排卵前卵泡细胞中的浓度(P<0.05)。将来自小窦状卵泡的培养颗粒细胞暴露于重组人TNFα(rhTNFα;0.06-6 nM)以剂量依赖性方式抑制E2分泌(P<0.01),但不影响P4分泌。此外,rhTNFα抑制细胞对促卵泡激素、福斯可林或二丁酰环磷腺苷诱导的P4和E2分泌(P<0.01)。这些结果表明,在小卵泡、排卵前卵泡和闭锁卵泡的牛颗粒细胞和卵泡膜细胞中存在功能性TNFα受体,并提示TNFα在调节其分泌功能中起作用。