首页> 外文期刊>FEBS Letters >Insulin‐like growth factor 1 and insulin reduce epidermal growth factor binding to Swiss 3T3 cells by an indirect mechanism that is apparently independent of protein kinase C
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Insulin‐like growth factor 1 and insulin reduce epidermal growth factor binding to Swiss 3T3 cells by an indirect mechanism that is apparently independent of protein kinase C

机译:胰岛素样生长因子1和胰岛素通过明显独立于蛋白激酶C的间接机制减少表皮生长因子与Swiss 3T3细胞的结合

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>Insulin-like growth factor 1 and insulin reduced the binding of 125I-labelled epidermal growth factor (125I-EGF) to Swiss 3T3 cells by 15–20% at 37°C, but not at 4°C. Scatchard analysis indicated that IGF-1 and insulin affected the higher-affinity component of EGF binding, an effect previously associated with the activation of protein kinase C. However, the inhibition of 125I-EGF binding by IGF-1 and insulin was increased, not reduced, when the cells were treated with high concentrations of phorbol esters to down-modulate protein kinase C. We suggest that IGF-1 and insulin activate a protein kinase with similar or overlapping specificity to that of protein kinase C.
机译:>胰岛素样生长因子1和胰岛素使 125 I标记的表皮生长因子( 125 I-EGF)与Swiss 3T3细胞的结合降低15–20 %在37°C而不是4°C时。斯卡查德分析表明,IGF-1和胰岛素影响了EGF结合的高亲和力成分,这种作用先前与蛋白激酶C的激活有关。但是,IGF抑制 125 I-EGF结合当用高浓度佛波酯处理细胞以降低蛋白激酶C时,-1且胰岛素增加而不是减少。我们建议IGF-1和胰岛素激活与蛋白具有相似或重叠特异性的蛋白激酶激酶C

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