Thams P, Capito K, Hedeskov C J
Diabetologia. 1986 Dec;29(12):888-92. doi: 10.1007/BF00870145.
The occurrence of polyamine-stimulated protein kinase (casein kinase II) in cytosol of mouse pancreatic islets was investigated. Islet protein phosphorylation was enhanced by spermidine, spermine, lysine-rich histone and polylysine; the major endogenous substrates in the cytosol were three proteins of Mr 50,000, 55,000 and 100,000. Cadaverine and putrescine were without effects. A Mr 100,000 protein is a major substrate for Ca2+-calmodulin-dependent protein kinase, and Mr 50,000 and 55,000 proteins are substrates for cyclic adenosine 3',5'-cyclic monophosphate (AMP) dependent protein kinase in mouse islets. However, neither cyclic-AMP-dependent protein kinase inhibitor nor trifluoperazine inhibited polyamine-enhanced protein phosphorylation. Both basal and polyamine-enhanced protein phosphorylation patterns were identical when either [gamma-32P] adenosine 5'-triphosphate (ATP) or [gamma-32P] guanosine 5'-triphosphate (GTP) was used as phosphate donors, indicative of the presence of a polyamine-stimulated casein kinase II in pancreatic islets. It is suggested that polyamines and polyamine-enhanced casein kinase II activity may have an important role in regulation of protein phosphorylation in pancreatic islets.
研究了小鼠胰岛细胞质中多胺刺激的蛋白激酶(酪蛋白激酶II)的存在情况。亚精胺、精胺、富含赖氨酸的组蛋白和聚赖氨酸可增强胰岛蛋白磷酸化;细胞质中的主要内源性底物是三种分子量分别为50,000、55,000和100,000的蛋白质。尸胺和腐胺无此作用。分子量为100,000的蛋白质是Ca2+ - 钙调蛋白依赖性蛋白激酶的主要底物,分子量为50,000和55,000的蛋白质是小鼠胰岛中环磷酸腺苷(cAMP)依赖性蛋白激酶的底物。然而,cAMP依赖性蛋白激酶抑制剂和三氟拉嗪均未抑制多胺增强的蛋白磷酸化。当使用[γ-32P]腺苷5'-三磷酸(ATP)或[γ-32P]鸟苷5'-三磷酸(GTP)作为磷酸盐供体时,基础和多胺增强的蛋白磷酸化模式相同,这表明胰岛中存在多胺刺激的酪蛋白激酶II。提示多胺和多胺增强的酪蛋白激酶II活性可能在胰岛蛋白磷酸化的调节中起重要作用。