Gavin J R, Roth J, Jen P, Freychet P
Proc Natl Acad Sci U S A. 1972 Mar;69(3):747-51. doi: 10.1073/pnas.69.3.747.
Human lymphocytes obtained from fasted adult subjects and cultured human tumor lymphocytes were investigated for specific insulin receptors. By use of monoiodoinsulin, specific insulin binding sites were demonstrated in peripheral human lymphocytes, cultured human lymphocytes, and in other types of human circulating cells. Insulins and insulin derivatives that varied in their potency to stimulate glucose oxidation in the fat cell and to inhibit binding of [(125)I]insulin to purified plasma membranes, varied in an analogous fashion in their ability to inhibit the binding of labeled insulin to human lymphocytes. Hormones that had no effect on the binding of insulin to fat cells or liver membranes also had no effect on the binding of insulin to lymphocytes. Binding was time and temperature dependent; dissociation of [(125)I]insulin was rapid upon addition of 10 muM insulin. These findings afford a direct approach to the study of endocrine disorders in man.
对从禁食成年受试者获取的人淋巴细胞以及培养的人肿瘤淋巴细胞进行了特定胰岛素受体的研究。通过使用单碘胰岛素,在外周血人淋巴细胞、培养的人淋巴细胞以及其他类型的人循环细胞中证实了特定的胰岛素结合位点。在脂肪细胞中刺激葡萄糖氧化以及抑制[(125)I]胰岛素与纯化质膜结合的效力不同的胰岛素和胰岛素衍生物,在抑制标记胰岛素与人淋巴细胞结合的能力方面也以类似方式存在差异。对胰岛素与脂肪细胞或肝细胞膜结合无影响的激素,对胰岛素与淋巴细胞的结合也无影响。结合具有时间和温度依赖性;加入10μM胰岛素后,[(125)I]胰岛素的解离很快。这些发现为研究人类内分泌紊乱提供了一种直接方法。