Tashima K, Yamamoto H, Setoyama C, Ono T, Miyamoto E
Department of Pharmacology, Kumamoto University School of Medicine, Japan.
J Neurochem. 1996 Jan;66(1):57-64. doi: 10.1046/j.1471-4159.1996.66010057.x.
To investigate the physiological role of Ca2+/calmodulin-dependent protein kinase II (CaM kinase II) in neuronal differentiation, we transfected the cDNA of the alpha subunit of mouse CaM kinase II (CaM kinase II alpha) into PC12 cells and established clonal cell lines that constitutively express the transfected CaM kinase II alpha gene. The expression of CaM kinase II alpha was confirmed by northern blot and immunoblot analyses. Northern blot analysis showed that the gamma and delta subunits of CaM kinase II are mainly expressed in PC12 cells. Treatment of the cells with ionomycin activated CaM kinase II alpha through autophosphorylation and generation of the Ca2+/calmodulin-dependent form. It is interesting that the neurite outgrowth induced by dibutyryl cyclic AMP was inhibited in these cell lines in accordance with the activities of overexpressed CaM kinase II alpha. The activity of cyclic AMP-dependent protein kinase showed similar levels among these cell lines. These results suggest that CaM kinase II is involved in the modulation of the neurite outgrowth induced by activation of the cyclic AMP system.
为了研究Ca2+/钙调蛋白依赖性蛋白激酶II(CaM激酶II)在神经元分化中的生理作用,我们将小鼠CaM激酶IIα亚基(CaM激酶IIα)的cDNA转染到PC12细胞中,并建立了组成性表达转染的CaM激酶IIα基因的克隆细胞系。通过Northern印迹和免疫印迹分析证实了CaM激酶IIα的表达。Northern印迹分析表明,CaM激酶II的γ和δ亚基主要在PC12细胞中表达。用离子霉素处理细胞通过自身磷酸化和产生Ca2+/钙调蛋白依赖性形式激活了CaM激酶IIα。有趣的是,在这些细胞系中,二丁酰环磷酸腺苷诱导的神经突生长根据过表达的CaM激酶IIα的活性受到抑制。环磷酸腺苷依赖性蛋白激酶的活性在这些细胞系中显示出相似的水平。这些结果表明,CaM激酶II参与了由环磷酸腺苷系统激活诱导的神经突生长的调节。