Ashkenazy-Shahar M, Ben-Porat H, Beitner R
Department of Life Sciences, Bar-Ilan University, Ramat Gan, 52900, Israel.
Mol Genet Metab. 1998 Nov;65(3):213-9. doi: 10.1006/mgme.1998.2759.
We report here a novel mechanism of insulin action in cultures of NIH-3T3 fibroblasts. Our experiments revealed that in these cells, insulin induced a rapid and transient increase in cytoskeleton-bound phosphofructokinase (EC 2.7.1.11), the rate-limiting enzyme in glycolysis, with a corresponding decrease in soluble (cytosolic) activity. Insulin also induced a slower increase in the levels of glucose 1,6-bisphosphate, the potent activator of cytosolic glycolysis. Both the rapid and the slower stimulatory actions of insulin were prevented by treatment with structurally different calmodulin antagonists, which strongly suggest that calmodulin is involved in these effects of insulin. The present and our previous experiments in muscle suggest that rapid, Ca2+-calmodulin-mediated increase in the binding of glycolytic enzymes to cytoskeleton, as well as the slower increase in glucose 1,6-bisphosphate, may be a general mechanism, in different cells, in signal transduction of insulin.
我们在此报告NIH-3T3成纤维细胞培养物中胰岛素作用的一种新机制。我们的实验表明,在这些细胞中,胰岛素可诱导糖酵解限速酶——细胞骨架结合型磷酸果糖激酶(EC 2.7.1.11)迅速且短暂地增加,同时可溶性(胞质)活性相应降低。胰岛素还可使糖酵解的强效激活剂1,6-二磷酸葡萄糖的水平缓慢升高。用结构不同的钙调蛋白拮抗剂处理可阻止胰岛素的快速和缓慢刺激作用,这强烈表明钙调蛋白参与了胰岛素的这些作用。我们目前以及之前在肌肉中的实验表明,糖酵解酶与细胞骨架结合的快速、Ca²⁺-钙调蛋白介导的增加以及1,6-二磷酸葡萄糖的缓慢增加,可能是不同细胞中胰岛素信号转导的一种普遍机制。