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首页> 外文期刊>Diabetologia >Inhibition of membrane depolarisation-induced transcriptional activity of cyclic AMP response element binding protein (CREB) by the dual-leucine-zipper-bearing kinase in a pancreatic islet beta cell line
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Inhibition of membrane depolarisation-induced transcriptional activity of cyclic AMP response element binding protein (CREB) by the dual-leucine-zipper-bearing kinase in a pancreatic islet beta cell line

机译:胰岛β细胞系中带有双亮氨酸拉链的激酶对膜去极化诱导的环AMP反应元件结合蛋白(CREB)转录活性的抑制

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摘要

The activation of the transcription factor cyclic AMP response element binding protein (CREB) by protein kinase A is inhibited by the human orthologue of the mitogen-activated protein kinase, dual-leucine-zipper-bearing kinase (DLK) in teratocarcinoma cells. However, pancreatic beta cells are electrically excitable and a major pathway regulating CREB in these cells is membrane depolarisation, leading to calcium influx and activation of the calcium/calmodulin-dependent protein phosphatase calcineurin. Therefore, the effect of DLK on CREB activity induced by membrane depolarisation was investigated in the beta cell line HIT.
机译:蛋白激酶A对转录因子环状AMP应答元件结合蛋白(CREB)的激活受到畸胎瘤癌细胞中人类有丝分裂原激活的蛋白激酶,双亮氨酸拉链激酶(DLK)的直系同源基因的抑制。但是,胰腺β细胞具有电刺激性,而在这些细胞中调节CREB的主要途径是膜去极化,从而导致钙大量涌入并激活钙/钙调蛋白依赖性蛋白磷酸酶钙调神经磷酸酶。因此,在β细胞系HIT中研究了DLK对膜去极化诱导的CREB活性的影响。

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