Hizuka N, Sukegawa I, Takano K, Asakawa K, Horikawa R, Tsushima T, Shizume K
Endocrinol Jpn. 1987 Feb;34(1):81-8. doi: 10.1507/endocrj1954.34.81.
Specific insulin-like growth factor I (IGF-I) receptors on a human erythroleukemia cell line (K-562 cells) were identified and characterized. [125I]-IGF-I specifically bound to K-562 cells and the binding was displaced by unlabeled IGF-I in a dose dependent manner, and half maximal inhibition of the binding was observed at 7 ng/ml IGF-I. [125I]IGF-I binding to the cells was displaced by multiplication stimulating activity (MSA) and by porcine insulin, with potencies that were 10, and 100 times less than that of IGF-I, respectively. By an affinity labeling technique, IGF type I receptors were found to be present in the K-562 cells. When the cells were differentiated by hemin (40 microM), specific binding of [125I]IGF-I to the cells was decreased to 56.8 +/- 5.0% of that for undifferentiated cells. Furthermore, at physiological concentration of IGF-I stimulated thymidine incorporation into DNA and increased the number of cells. These data demonstrate that K-562 cells have specific receptors for IGF-I which may be functionally important for these cells, and that the IGF-I binding sites decrease with cell differentiation. This system might be useful in studying the interaction of IGF-I receptors.
在人红白血病细胞系(K - 562细胞)上鉴定并表征了特异性胰岛素样生长因子I(IGF - I)受体。[125I] - IGF - I特异性结合K - 562细胞,且未标记的IGF - I以剂量依赖方式取代该结合,在7 ng/ml IGF - I时观察到结合的半数最大抑制。[125I]IGF - I与细胞的结合被增殖刺激活性(MSA)和猪胰岛素取代,其效力分别比IGF - I低10倍和100倍。通过亲和标记技术,发现K - 562细胞中存在I型IGF受体。当细胞用血红素(40 microM)分化时,[125I]IGF - I与细胞的特异性结合降至未分化细胞的56.8 +/- 5.0%。此外,在IGF - I的生理浓度下,刺激了胸腺嘧啶核苷掺入DNA并增加了细胞数量。这些数据表明,K - 562细胞具有IGF - I的特异性受体,这对这些细胞可能具有功能重要性,并且IGF - I结合位点随细胞分化而减少。该系统可能有助于研究IGF - I受体的相互作用。