Fitz T A, Hoyer P B, Niswender G D
Prostaglandins. 1984 Jul;28(1):119-26. doi: 10.1016/0090-6980(84)90119-9.
Preparations of small and large steroidogenic cells from enzymatically dispersed ovine corpora lutea were utilized to study the in vitro effects of luteinizing hormone (LH) and prostaglandins (PG) E1, E2 and I2. Cells were allowed to attach to culture dishes overnight and were incubated with either LH (100 ng/ml), PGE1, PGE2, or PGI2 (250 ng/ml each). The secretion of progesterone by large cells was stimulated by all prostaglandins tested (P less than 0.05) while the moderate stimulation observed after LH treatment was attributable to contamination of the large cell population with small cells. Prostaglandins E1 and E2 had no effect on progesterone secretion by small cells, while LH was stimulatory at all times (0.5 to 4 hr) and PGI2 was stimulatory by 4 hr. Additional studies were conducted to determine if the effects of PGE2 upon steroidogenesis in large cells were correlated with stimulated activity of adenylate cyclase. In both plated and suspended cells PGE2 caused an increase (P less than 0.05) in the rate of progesterone secretion but had no effect upon the activity of adenylate cyclase or cAMP concentrations within cells or in the incubation media. Exposure of luteal cells to forskolin, a nonhormonal stimulator of adenylate cyclase, resulted in marked increases in all parameters of cyclase activity but had no effect on progesterone secretion. These data suggest that the actions of prostaglandins E1, E2 and I2 are directed primarily toward the large cells of the ovine corpus luteum and cast doubt upon the role of adenylate cyclase as the sole intermediary in regulation of progesterone secretion in this cell type.
利用酶解分散的绵羊黄体制备的小、大类固醇生成细胞,研究促黄体生成素(LH)和前列腺素(PG)E1、E2及I2的体外效应。细胞在培养皿中贴壁过夜,然后分别与LH(100 ng/ml)、PGE1、PGE2或PGI2(各250 ng/ml)一起孵育。所有测试的前列腺素均刺激大细胞分泌孕酮(P<0.05),而LH处理后观察到的适度刺激归因于大细胞群体被小细胞污染。前列腺素E1和E2对小细胞分泌孕酮无影响,而LH在所有时间(0.5至4小时)均有刺激作用,PGI2在4小时时有刺激作用。进行了额外研究以确定PGE2对大细胞类固醇生成的影响是否与腺苷酸环化酶的刺激活性相关。在贴壁细胞和悬浮细胞中,PGE2均导致孕酮分泌速率增加(P<0.05),但对腺苷酸环化酶活性或细胞内及孵育培养基中的cAMP浓度无影响。黄体细胞暴露于腺苷酸环化酶的非激素刺激剂福斯高林后,环化酶活性的所有参数均显著增加,但对孕酮分泌无影响。这些数据表明,前列腺素E1、E2和I2的作用主要针对绵羊黄体的大细胞,并对腺苷酸环化酶作为该细胞类型中孕酮分泌调节的唯一中介的作用提出了质疑。