Cascieri M A, Chicchi G G, Hayes N S, Strader C D
Biochim Biophys Acta. 1986 May 29;886(3):491-9. doi: 10.1016/0167-4889(86)90186-2.
The murine non-fusing muscle cell line contains distinct receptors for insulin and insulin-like growth factors. Pretreatment of myocytes with insulin for 20 h at 37 degrees C inhibits the binding of [125I]iodoinsulin by 60% without affecting the binding of [125I]iodoinsulin-like growth factor I. The ED50 values for down-regulation of the insulin and insulin-like growth factor receptor by their respective ligands are 1 nM and 3 nM, respectively. Insulin, (Thr-59)-insulin-like growth factor I and multiplication-stimulating activity stimulate 2-[3H]deoxyglucose transport in myocytes with ED50 values of 5 nM, 5.6 nM and 33 nM, respectively. In order to determine whether (Thr-59)-insulin-like growth factor I stimulates 2-[3H]deoxyglucose transport in myocytes via its own receptor or the insulin receptor, we determined the activity of these peptides after down-regulation of the insulin receptor. The rate of 2-[3H]deoxyglucose transport in myocytes pretreated with insulin (5 nM) is elevated but returns to control levels by 1 h after the washout of insulin. The dose-response curve for insulin-stimulated 2-[3H]deoxyglucose transport is shifted to the right (ED50 greater than 100 nM) immediately after insulin washout but is normal by 1 h after insulin washout. In contrast, the dose-response curve for (Thr-59)-insulin-like growth factor I is unchanged in insulin-pretreated cells immediately after insulin washout. These data show that (Thr-59)-insulin-like growth factor I stimulates 2-[3H]deoxyglucose transport in myocytes by acting through an insulin-like growth factor receptor and not through the insulin receptor. Since multiplication-stimulating activity is 6-fold less active than (Thr-59)-insulin-like growth factor, they both may be acting through a type 1 insulin-like growth factor receptor.
小鼠非融合性肌肉细胞系含有胰岛素和胰岛素样生长因子的不同受体。在37℃下用胰岛素预处理心肌细胞20小时可使[125I]碘胰岛素的结合抑制60%,而不影响[125I]碘胰岛素样生长因子I的结合。胰岛素和胰岛素样生长因子各自的配体对其受体下调的ED50值分别为1 nM和3 nM。胰岛素、(苏氨酸-59)-胰岛素样生长因子I和增殖刺激活性分别以5 nM、5.6 nM和33 nM的ED50值刺激心肌细胞中的2-[3H]脱氧葡萄糖转运。为了确定(苏氨酸-59)-胰岛素样生长因子I是通过其自身受体还是胰岛素受体刺激心肌细胞中的2-[3H]脱氧葡萄糖转运,我们在胰岛素受体下调后测定了这些肽的活性。用胰岛素(5 nM)预处理的心肌细胞中2-[3H]脱氧葡萄糖的转运速率升高,但在胰岛素洗脱后1小时恢复到对照水平。胰岛素洗脱后立即,胰岛素刺激的2-[3H]脱氧葡萄糖转运的剂量反应曲线向右移动(ED50大于100 nM),但在胰岛素洗脱后1小时恢复正常。相反,在胰岛素洗脱后,胰岛素预处理细胞中(苏氨酸-59)-胰岛素样生长因子I的剂量反应曲线没有变化。这些数据表明,(苏氨酸-59)-胰岛素样生长因子I通过胰岛素样生长因子受体而非胰岛素受体刺激心肌细胞中的2-[3H]脱氧葡萄糖转运。由于增殖刺激活性比(苏氨酸-59)-胰岛素样生长因子的活性低6倍,它们可能都通过1型胰岛素样生长因子受体起作用。