Ottobre J S, Stouffer R L
Endocrinology. 1986 Oct;119(4):1594-602. doi: 10.1210/endo-119-4-1594.
Stimulation of the primate corpus luteum (CL) by endogenous CG in early pregnancy or by exogenous hCG in simulated early pregnancy is transient, possibly due to a drop in the number of available gonadotropin receptors in the CL. The objective of the current study was to determine if this reduction in available CG receptors in the CL is due to down-regulation of the total receptor population or occupation of receptors by CG. CL were removed from rhesus monkeys (n = 27) during prolonged CG exposure in simulated early pregnancy. Luteal tissue was homogenized, and a particulate preparation (20,000 g) was formed. Bound gonadotropin was eluted from half of each tissue preparation with 0.05 M Na acetate-HCl in 0.1% gelatin (pH 3.3); the other half was treated with control buffer (0.05 M Tris-HCl, pH7.4). The hCG in the eluate was quantified by RIA and used to estimate the number of occupied receptors. Numbers and affinities of receptors were estimated by Scatchard analyses of specific [125I]hCG binding. Serum concentrations of progesterone increased within 9 h of hCG treatment and declined between 3 and 10 days of treatment. Whereas the number of available receptors declined from 0 h to 10 days of hCG treatment, the number of receptors occupied by hCG increased throughout treatment from 0.19 +/- 0.01 fmol/mg tissue (mean +/- SE) after 2 h of treatment to 7.76 +/- 1.73 fmol/mg after 10 days of treatment (P less than 0.05). The total number of receptors (available plus occupied) did not change throughout the 10-day treatment period (11.93 +/- 2.11 fmol/mg at 0 h vs. 9.64 +/- 1.86 at 10 days; P greater than 0.10). The dissociation constants (Kd) for CG binding were greater (P less than 0.05) after 6 days (4.10 +/- 0.57 X 10(-10) M) and 10 days (5.24 +/- 0.54 X 10(-10) M) of treatment than after 0-3 days (0.95 +/- 0.06 X 10(-10) M) of treatment. Notably, the percentage of total receptors able to rebind hCG after elution declined from 0 h (79.0 +/- 5.4%) to 10 days (23.0 +/- 3.2%; P less than 0.05). Rebindability was highly correlated with the number of available (r = 0.906; P less than 0.05) and occupied (r = -0.999; P less than 0.01) CG receptors. Thus, the reduction in available gonadotropin-binding sites in the CL during simulated early pregnancy is largely due to occupancy rather than down-regulation of receptors.(ABSTRACT TRUNCATED AT 400 WORDS)
在妊娠早期,内源性绒毛膜促性腺激素(CG)对灵长类动物黄体(CL)的刺激,或在模拟早期妊娠时外源性人绒毛膜促性腺激素(hCG)对其的刺激都是短暂的,这可能是由于黄体中可用促性腺激素受体数量下降所致。本研究的目的是确定黄体中可用CG受体数量的减少是由于总受体群体的下调还是由于CG占据了受体。在模拟早期妊娠中长时间暴露于CG期间,从恒河猴(n = 27)身上取出黄体。将黄体组织匀浆,形成微粒体制剂(20,000g)。用0.05M醋酸钠 - 盐酸在0.1%明胶(pH 3.3)中从每个组织制剂的一半中洗脱结合的促性腺激素;另一半用对照缓冲液(0.05M Tris - 盐酸,pH7.4)处理。通过放射免疫分析(RIA)对洗脱液中的hCG进行定量,并用于估计被占据受体的数量。通过对特异性[125I]hCG结合进行Scatchard分析来估计受体的数量和亲和力。hCG治疗后9小时内血清孕酮浓度升高,治疗3至10天之间下降。虽然从hCG治疗0小时到10天可用受体数量下降,但在整个治疗过程中,被hCG占据的受体数量从治疗2小时后的0.19±0.01 fmol/mg组织(平均值±标准误)增加到治疗10天后的7.76±1.73 fmol/mg(P<0.05)。在整个10天的治疗期内,受体总数(可用的加上被占据的)没有变化(0小时时为11.93±2.11 fmol/mg,10天时为9.64±1.86;P>0.10)。治疗6天(4.10±0.57×10^(-10)M)和10天(5.24±0.54×10^(-10)M)后CG结合的解离常数(Kd)比治疗0至3天(0.95±0.06×10^(-10)M)后更大(P<0.05)。值得注意的是,洗脱后能够重新结合hCG的总受体百分比从0小时的(79.0±5.4%)下降到10天的(23.0±3.2%;P<0.05)。重新结合能力与可用CG受体数量(r = 0.906;P<0.05)和被占据CG受体数量(r = -0.999;P<0.01)高度相关。因此,在模拟早期妊娠期间黄体中可用促性腺激素结合位点的减少主要是由于受体被占据而非受体下调。(摘要截断于400字)