McNatty K P, O'Keeffe L E, Henderson K M, Heath D A, Lun S
J Reprod Fertil. 1986 Jul;77(2):477-88. doi: 10.1530/jrf.0.0770477.
Specific receptors for 125I-labelled hCG in ovarian follicle wall were located in the theca interna. No specific binding of 125I-labelled hCG was found in theca externa and/or stromal tissue. The kinetics of 125I-labelled hCG binding to theca interna followed second order kinetics with calculated association rate constants (ka +/- s.d.) of 1.57 +/- 0.16 X 10(6) and 0.57 +/- 0.02 X 10(6) litres mol-1 sec-1 at 37 degrees C and 22 degrees C respectively. Dissociation of specifically bound 125I-labelled hCG from theca interna was minimal at 37 degrees C and 22 degrees C. The binding of 125I-labelled hCG to theca interna could be displaced with PMSG, FSH-P and sheep LH but other sheep pituitary hormones and LH-releasing hormone showed little or no cross-reaction. The calculated binding capacities (Bmax) and equilibrium dissociation constants (Kd) for 125I-labelled hCG binding to theca interna did not differ between Romney ewes and Booroola x Romney ewes with and without the fecundity (F) gene on Day 10 of the oestrous cycle, during anoestrus or at 36 h after an injection of cloprostenol on Day 10 of the oestrous cycle. When the data for Day 10 and anoestrus were pooled, the median (range) Bmax and Kd values in non-atretic follicles (greater than or equal to 3 mm diameter) were 12.0 (5.1-23.5) fmol/mg protein and 0.10 (0.05-0.16) nM respectively. At 36 h after cloprostenol injection the respective median (range) Bmax and Kd values in non-atretic follicles (greater than or equal to 3 mm diam.) increased to 46.9 (28.4-70.3) fmol/mg protein and 0.23 (0.13-0.65) nM respectively. In corpora lutea the hCG binding characteristics were similar in all the above breeds/genotypes. On Day 10 of the cycle, the mean Bmax but not the mean Kd value was significantly higher (P less than 0.01) than the corresponding value at 36 h after cloprostenol injection. In granulosa cells, from follicles of greater than or equal to 5 mm diameter of Romney and Booroola x Romney (++) ewes and from follicles of greater than or equal to 3 mm diameter of Booroola x Romney (F+) ewes, the hCG binding characteristics were similar. In granulosa cells from smaller sized follicles from the above breeds/genotypes, no specific hCG binding was noted.
卵巢卵泡壁中125I标记的人绒毛膜促性腺激素(hCG)的特异性受体位于卵泡内膜。在卵泡外膜和/或间质组织中未发现125I标记的hCG的特异性结合。125I标记的hCG与卵泡内膜结合的动力学遵循二级动力学,在37℃和22℃时计算的缔合速率常数(ka±标准差)分别为1.57±0.16×10(6)和0.57±0.02×10(6)升·摩尔-1·秒-1。在37℃和22℃时,特异性结合的125I标记的hCG从卵泡内膜的解离极少。125I标记的hCG与卵泡内膜的结合可被孕马血清促性腺激素(PMSG)、促卵泡素-P(FSH-P)和绵羊促黄体生成素(LH)取代,但其他绵羊垂体激素和促黄体生成素释放激素显示很少或没有交叉反应。在发情周期第10天、乏情期或发情周期第10天注射氯前列醇后36小时,罗姆尼母羊和携带或不携带繁殖力(F)基因的布鲁拉×罗姆尼母羊中,125I标记的hCG与卵泡内膜结合的计算结合容量(Bmax)和平衡解离常数(Kd)没有差异。当合并第10天和乏情期的数据时,直径大于或等于3mm的非闭锁卵泡中的中位数(范围)Bmax和Kd值分别为12.0(5.1-23.5)fmol/mg蛋白质和0.10(0.05-0.16)nM。注射氯前列醇后36小时,直径大于或等于3mm的非闭锁卵泡中的相应中位数(范围)Bmax和Kd值分别增加到46.9(28.4-70.