Maassen J A, Klinkhamer M P, Odink R J, Sips H, van der Zon G C, Wieringa T, Krans H M, Möller W
Department of Medical Biochemistry, Sylvius Laboratories Leiden, The Netherlands.
Eur J Biochem. 1988 Mar 15;172(3):725-9. doi: 10.1111/j.1432-1033.1988.tb13949.x.
Leprechaunism is an inherited human disorder characterized by severe insulin resistance. We have examined the properties of the insulin receptor in fibroblasts from a leprechaun patient. In vitro, severe insulin resistance is reflected by a low level of insulin binding to the patients fibroblasts and impaired insulin-mediated uptake of 2-deoxyglucose. Quantification of the receptor in detergent-solubilized total glycoprotein indicates a normal receptor number, in agreement with the observed normal level of insulin receptor mRNA on northern blots. The insulin-stimulated autophosphorylation of the patient's receptor shows a normal profile. The insulin receptor is present on the plasma membrane as indicated by cell-surface iodination experiments. No abnormalities in the molecular masses of the receptor's alpha and beta chains were observed. The results indicate that an apparently normal receptor is synthesized in sufficient amounts but functional expression of the receptor on the plasma membrane is impaired.
妖精貌综合征是一种以严重胰岛素抵抗为特征的遗传性人类疾病。我们研究了一名妖精貌患者成纤维细胞中胰岛素受体的特性。在体外,严重的胰岛素抵抗表现为胰岛素与患者成纤维细胞的结合水平较低,以及胰岛素介导的2-脱氧葡萄糖摄取受损。对去污剂溶解的总糖蛋白中的受体进行定量分析表明受体数量正常,这与Northern印迹上观察到的胰岛素受体mRNA正常水平一致。患者受体的胰岛素刺激的自身磷酸化显示出正常的模式。细胞表面碘化实验表明胰岛素受体存在于质膜上。未观察到受体α链和β链分子量的异常。结果表明,合成了足够数量的看似正常的受体,但该受体在质膜上的功能性表达受损。