Furlanetto R W, Underwood L E, Van Wyk J J, D'Ercole A J
J Clin Invest. 1977 Sep;60(3):648-57. doi: 10.1172/JCI108816.
The development of a radioimmunoassay for somatomedin-C has for the first time made it possible to discriminate between serum concentrations of a single peptide or closely related group of peptides and the net somatomedin activity measured by less specific bioassay and radioreceptor techniques. Antibodies to human somatomedin-C were raised in rabbits using a somatomedin-C ovalbumin complex as the antigen. A variety of peptide hormones at concentrations up to 1 muM are not recognized by the antibody. Insulin at concentrations >0.1 muM cross reacts in a non-parallel fashion; purified somatomedin-A is only 3% as active as somatomedin-C; and radiolabeled cloned rat liver multiplication stimulating activity does not bind to the antibody. Immunoreactive somatomedin-C can also be quantitated in the sera of a variety of subhuman species. Unusual assay kinetics, which are manifest when reactants are incubated under classic "equilibrium" assay conditions, appear to result from the failure of (125)I-somatomedin-C to readily equilibrate with the somatomedin-C serum binding protein complex. It is, therefore, necessary to use nonequilibrium assay conditions to quantitate somatomedin-C in serum. With this assay it is possible to detect somatomedin-C in normal subjects using as little as 0.25 mul of unextracted serum. Serum somatomedin-C concentrations in normal subjects were lowest in cord blood and rose rapidly during the first 4 yr of life to near adult levels. In 23 normal adult volunteers, the mean serum somatomedin-C concentration was 1.50+/-0.10 U/ml (SEM) when compared to a pooled adult serum standard. 19 children with hypopituitary dwarfism had concentrations below 0.20 U/ml. 17 of these were below 0.1 U/ml, the lower limit of sensitivity of the assay. The mean concentration in 14 adults with active acromegaly was 6.28+/-0.37 U/ml (SEM), five times greater than the normal volunteers. Significant increases in serum somatomedin-C concentrations were observed in 8 of 10 hypopituitary children within 72 h after the parenteral administration of human growth hormone. Three patients with Cushing's disease had elevated serum somatomedin-C concentrations (2.61+/-0.14 U/ml [SEM]). Three patients with hyperprolactinemia had normal concentrations (1.74+/-0.11 U/ml [SEM]).The important new discovery brought to light by quantitation of immunoassayable somatomedin in patient sera is that all previously used assays detect, in addition to somatomedin-C, serum substances that are not under as stringent growth hormone control.
生长调节素-C放射免疫分析法的发展首次使得区分单一肽或紧密相关肽组的血清浓度与通过特异性较低的生物测定法和放射受体技术测得的生长调节素净活性成为可能。以生长调节素-C卵清蛋白复合物作为抗原,在兔体内产生了抗人生长调节素-C的抗体。浓度高达1μM的多种肽激素都不被该抗体识别。浓度>0.1μM的胰岛素以非平行方式发生交叉反应;纯化的生长调节素-A的活性仅为生长调节素-C的3%;放射性标记的克隆大鼠肝脏增殖刺激活性不与该抗体结合。免疫反应性生长调节素-C也可在多种非人灵长类动物的血清中进行定量。当反应物在经典的“平衡”测定条件下孵育时出现的异常测定动力学,似乎是由于¹²⁵I-生长调节素-C未能与生长调节素-C血清结合蛋白复合物迅速达到平衡所致。因此,有必要使用非平衡测定条件来定量血清中的生长调节素-C。使用这种测定法,仅用0.25μl未提取的血清就有可能在正常受试者中检测到生长调节素-C。正常受试者的血清生长调节素-C浓度在脐血中最低,并在生命的头4年迅速上升至接近成人水平。在23名正常成年志愿者中,与混合成人血清标准品相比,平均血清生长调节素-C浓度为1.50±0.10U/ml(标准误)。19名垂体功能减退性侏儒症儿童的浓度低于0.20U/ml。其中17名低于0.1U/ml,即该测定法的灵敏度下限。14名活动性肢端肥大症成人的平均浓度为6.28±0.37U/ml(标准误),是正常志愿者的5倍。在10名垂体功能减退儿童中,有8名在胃肠外注射人生长激素后72小时内血清生长调节素-C浓度显著升高。3例库欣病患者的血清生长调节素-C浓度升高(2.61±0.14U/ml[标准误])。3例高催乳素血症患者的浓度正常(1.74±0.11U/ml[标准误])。通过对患者血清中可免疫测定的生长调节素进行定量所揭示的重要新发现是,所有先前使用的测定法除了检测生长调节素-C外,还检测不受生长激素严格控制的血清物质。