Behan D P, Khongsaly O, Liu X J, Ling N, Goland R, Nasman B, Olsson T, De Souza E B
Neurocrine Biosciences, Inc., San Diego, California 92121, USA.
J Clin Endocrinol Metab. 1996 Jul;81(7):2579-86. doi: 10.1210/jcem.81.7.8675581.
The actions of human corticotropin-releasing factor (hCRF) in brain, pituitary, and plasma are modulated by a 37-kDa protein [CRF-binding protein (CRF-BP)] that binds to hCRF and neutralizes the peptide's biological activity, suggesting that only the free unbound peptide is biologically active. To accurately predict the biological consequences resulting from changes in total hCRF levels, we have developed two-site enzyme-linked immunosorbent assays (ELISAs) for hCRF-BP, free hCRF, and the hCRF-BP/hCRF complex. The assays were validated by measuring each factor in 1) maternal plasma at times when CRF and hCRF-BP levels are altered, and 2) plasma from normal elderly human subjects who have undergone a hCRF stimulation test. The hCRF-BP ELISA has a sensitivity of 2.7 fmol and a range of detection from 2.7-8000 fmol. Both the hCRF and hCRF-BP/ hCRF assays have a sensitivity of 0.4 fmol, with a useful range of detection from 0.4-40 fmol. Maternal plasma hCRF-BP levels remained unaltered between the 16-21 and 34-39 month gestational age groups. However, levels rose from 0.88 +/- 0.069 nmol/L in the 16-21 month gestational age group to 1.01 +/- 0.09 nmol/L in the 28-33 month gestational age group. Bound hCRF levels dramatically rose from undetectable at 16-21 months of gestation to 200 +/- 69 and 442 +/- 106 pmol/L in the 28-33 and 34-39 month gestational age groups, respectively. In comparison, free hCRF levels remained low throughout gestation, but dramatically rose to 318 +/- 120 pmol/L from 34-39 months of gestation. Binding site occupancy on the hCRF-BP decreased when bound and free hCRF levels were elevated. After treating the third trimester plasma sample with the high affinity hCRF-BP ligand, alpha-helical CRF-(9-41), all of the bound hCRF was displaced from the binding protein, and free hCRF levels rose from 87 to 284 pmol/L. The plasma hCRF-BP level was 0.9 +/- 0.08 nmol/L in normal human volunteers (10 men and 9 women; mean +/- SD age, 74.2 +/- 7.7 yr), decreased to 60% of basal levels 15 min after a bolus injection of 1 microgram/kg synthetic hCRF, and gradually returned to preinjection levels after 120 min. Conversely, bound and free hCRF levels increased from undetectable levels before hCRF injection to 0.58 +/- 0.03 nmol/L at 15 min and then rapidly decreased to undetectable levels at 120 min. These data validate the ELISAs in combination with high affinity hCRF-BP ligands for measuring bound and free hCRF in human plasma and suggest the utility of these assays for further determining alterations in peripheral CRF in conditions such as pregnancy.
人促肾上腺皮质激素释放因子(hCRF)在脑、垂体和血浆中的作用受到一种37 kDa蛋白质[CRF结合蛋白(CRF - BP)]的调节,该蛋白与hCRF结合并中和其生物活性,这表明只有游离未结合的肽具有生物活性。为了准确预测hCRF总水平变化所导致的生物学后果,我们开发了用于检测hCRF - BP、游离hCRF和hCRF - BP/hCRF复合物的双位点酶联免疫吸附测定法(ELISA)。通过在以下两种情况下测量各因子来验证这些测定法:1)在CRF和hCRF - BP水平发生变化时的母体血浆;2)来自接受hCRF刺激试验的正常老年人类受试者的血浆。hCRF - BP ELISA的灵敏度为2.7 fmol,检测范围为2.7 - 8000 fmol。hCRF和hCRF - BP/hCRF测定法的灵敏度均为0.4 fmol,有效检测范围为0.4 - 40 fmol。在妊娠16 - 21个月和34 - 39个月的胎龄组之间,母体血浆hCRF - BP水平保持不变。然而,其水平从妊娠16 - 21个月胎龄组的0.88±0.069 nmol/L升至妊娠28 - 33个月胎龄组的1.01±0.09 nmol/L。结合型hCRF水平从妊娠16 - 21个月时的不可检测显著升至妊娠28 - 33个月胎龄组的200±69 pmol/L和妊娠34 - 39个月胎龄组的442±106 pmol/L。相比之下,游离hCRF水平在整个妊娠期都保持较低,但从妊娠34 - 39个月时急剧升至318±120 pmol/L。当结合型和游离型hCRF水平升高时,hCRF - BP上的结合位点占有率降低。用高亲和力的hCRF - BP配体α - 螺旋CRF - (9 - 41)处理妊娠晚期血浆样本后,所有结合型hCRF都从结合蛋白上被置换出来,游离hCRF水平从87 pmol/L升至284 pmol/L。正常人类志愿者(10名男性和9名女性;平均±标准差年龄,74.2±7.7岁)的血浆hCRF - BP水平为0.9±0.08 nmol/L,静脉注射1 μg/kg合成hCRF后15分钟降至基础水平的60%,120分钟后逐渐恢复到注射前水平。相反,结合型和游离型hCRF水平从hCRF注射前的不可检测水平升至15分钟时的0.58±0.03 nmol/L,然后在120分钟时迅速降至不可检测水平。这些数据验证了结合高亲和力hCRF - BP配体的ELISA用于测量人血浆中结合型和游离型hCRF的有效性,并表明这些测定法在进一步确定妊娠等情况下外周CRF变化方面的实用性。