Tonetta S A, Yanagihara D L, DeVinna R S, diZerega G S
Livingston Reproductive Biology Laboratory, Department of Obstetrics and Gynecology, University of Southern California School of Medicine, Los Angeles 90033.
Biol Reprod. 1988 Jun;38(5):1001-5. doi: 10.1095/biolreprod38.5.1001.
Follicle-regulatory protein (FRP) affects ovarian steroidogenesis and thus follicular maturation. However, secretion of FRP by cells from different-sized follicles as well as the modulation of FRP production by gonadotropins and locally produced steroids are unknown. To evaluate which cell type secretes FRP, theca and granulosa cells were obtained from porcine follicles. In addition, the effects of follicle-stimulating hormone (FSH) and steroids on FRP secretion from granulosa cells of small (less than 3 mm), medium (3-6 mm), and large (greater than 8 mm) porcine follicles and theca cells of large follicles were determined. Granulosa cells were obtained from follicular aspirates, whereas theca cells were recovered after digestion of the stereomicroscopically removed thecal layer. Both were cultured in monolayer in serum-free medium. Granulosa cells were treated as follows: 1) control; 2) FSH (250 ng/ml); 3) progesterone (500 ng/ml, 3 micrograms/ml), or estradiol-17 beta (500 ng/ml, 4 micrograms/ml), or dihydrotestosterone (500 ng/ml, 1 microgram/ml); 4) FSH + progesterone, or estradiol-17 beta, or dihydrotestosterone. Theca cells received the same treatment except that human chorionic gonadotropin (hCG) (5m IU/ml) was used in place of FSH. At 48 or 96 h, media were removed and FRP was quantitated by an Enzyme-Linked Immunosorbent Assay (ELISA). FRP was identified in granulosal medium from follicles of all sizes, but was not present in thecal cultures. At 48 h, granulosa cells from small and medium-sized follicles produced more FRP (20.04 +/- 4.4, 35.42 +/- 4.1 immunoreactive units [IRU]) than cells from large (3.53 +/- 0.97 IRU) follicles.(ABSTRACT TRUNCATED AT 250 WORDS)
卵泡调节蛋白(FRP)影响卵巢类固醇生成,进而影响卵泡成熟。然而,不同大小卵泡的细胞分泌FRP的情况以及促性腺激素和局部产生的类固醇对FRP产生的调节尚不清楚。为了评估哪种细胞类型分泌FRP,从猪卵泡中获取了卵泡膜细胞和颗粒细胞。此外,还测定了促卵泡激素(FSH)和类固醇对小(小于3毫米)、中(3 - 6毫米)、大(大于8毫米)猪卵泡颗粒细胞以及大卵泡卵泡膜细胞分泌FRP的影响。颗粒细胞从卵泡抽吸物中获取,而卵泡膜细胞在立体显微镜下移除卵泡膜层后经消化回收。二者均在无血清培养基中单层培养。颗粒细胞的处理如下:1)对照;2)FSH(250纳克/毫升);3)孕酮(500纳克/毫升,3微克/毫升),或雌二醇 - 17β(500纳克/毫升,4微克/毫升),或双氢睾酮(500纳克/毫升,1微克/毫升);4)FSH + 孕酮,或雌二醇 - 17β,或双氢睾酮。卵泡膜细胞接受相同处理,只是用人绒毛膜促性腺激素(hCG)(5毫国际单位/毫升)代替FSH。在48或96小时时,去除培养基,通过酶联免疫吸附测定(ELISA)对FRP进行定量。在所有大小卵泡的颗粒细胞培养基中均鉴定出FRP,但在卵泡膜细胞培养物中未检测到。在48小时时,中小卵泡的颗粒细胞产生的FRP(20.04±4.4、35.42±4.1免疫反应单位[IRU])比大卵泡(3.53±0.97 IRU)的颗粒细胞多。(摘要截断于250字)