Jääskeläinen K
Mol Cell Endocrinol. 1982 Apr;26(1-2):129-39. doi: 10.1016/0303-7207(82)90011-9.
The catabolism of human choriogonadotropin (hCG) in rat preovulatory granulosa cells and follicular fluid was studied in order to elucidate the mechanisms responsible for the removal of receptor-hCG complexes. Rats pretreated with pregnant mare serum gonadotropin (PMSG) were injected i.v. with 125I-labelled hCG with or without unlabelled hCG a few hours before the surge of endogenous preovulatory gonadotropin. The radioactive components of granulosa cells and of follicular fluid were characterized by filtration through Sepharose-6B gel. Granulosa cells catabolized receptor-bound 125I-hCG to hormone sub-units; however, the rate of catabolism in vivo was relatively slow. Receptor-125I-hCG complex also appeared in the follicular fluid. Binding of 125I-labelled hCG to receptor molecules of follicular fluid in vivo was time-dependent and it was inhibited by smaller amounts of unlabelled hCG than the binding, in vivo, of 125I-labelled hCG to the receptors of granulosa cells. Both follicular fluid and granulosa cell homogenate, in vitro, catabolized 125I-labelled hCG to hormone sub-units.
为了阐明负责清除受体 - 人绒毛膜促性腺激素(hCG)复合物的机制,研究了大鼠排卵前颗粒细胞和卵泡液中hCG的分解代谢。用孕马血清促性腺激素(PMSG)预处理的大鼠在体内内源性排卵前促性腺激素激增前数小时静脉注射125I标记的hCG,同时或不注射未标记的hCG。颗粒细胞和卵泡液的放射性成分通过Sepharose - 6B凝胶过滤进行表征。颗粒细胞将受体结合的125I - hCG分解为激素亚基;然而,体内分解代谢速率相对较慢。受体 - 125I - hCG复合物也出现在卵泡液中。体内125I标记的hCG与卵泡液受体分子的结合是时间依赖性的,并且与体内125I标记的hCG与颗粒细胞受体的结合相比,较小量的未标记hCG即可抑制这种结合。体外,卵泡液和颗粒细胞匀浆都将125I标记的hCG分解为激素亚基。