Horie Yuki, Arame Toshiaki, Hirashima Naohide, Tanaka Masahiko
Department of Cellular Biophysics, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603, Japan.
Department of Cellular Biophysics, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603, Japan.
Neuroscience. 2021 Mar 15;458:87-98. doi: 10.1016/j.neuroscience.2021.01.024. Epub 2021 Jan 23.
Cerebellar Purkinje cells develop the most elaborate dendritic trees among neurons in the brain. To examine the role of Ca/calmodulin-dependent protein kinase (CaMK) IIα, IIβ and IV in the dendritic differentiation of Purkinje cells, we introduced siRNA against these CaMKs into Purkinje cells in cerebellar cell cultures using a single-cell electroporation technique. Single-cell electroporation enables us to transfer siRNA into specific cells within a heterogeneous cell population. In addition, we can easily and reliably transfer multiple types of siRNA into a cell simply by loading them together in one micropipette. Any one of the siRNA against CaMKIIα, IIβ and IV (single knockdown) or any combinations of two of the siRNA against these CaMKs (double knockdown) had no significant effects on the dendritic differentiation of Purkinje cells. However, the combination of all three siRNA against these CaMKs (triple knockdown) inhibited the branching of Purkinje cell dendrites. Furthermore, the triple knockdown reduced the phosphorylation of CREB in Purkinje cells. These findings suggest the promotion of dendritic differentiation of Purkinje cells by CaMKIIα, IIβ and IV and the possible involvement of phosphorylation of CREB as a common substrate of these CaMKs.
小脑浦肯野细胞在大脑神经元中发育出最为复杂的树突分支。为了研究钙/钙调蛋白依赖性蛋白激酶(CaMK)IIα、IIβ和IV在浦肯野细胞树突分化中的作用,我们使用单细胞电穿孔技术将针对这些CaMK的小干扰RNA(siRNA)导入小脑细胞培养物中的浦肯野细胞。单细胞电穿孔使我们能够将siRNA导入异质细胞群体中的特定细胞。此外,我们只需将多种类型的siRNA一起加载到一个微量移液器中,就能轻松且可靠地将它们导入一个细胞。针对CaMKIIα、IIβ和IV的任何一种siRNA(单基因敲低)或针对这些CaMK的两种siRNA的任何组合(双基因敲低)对浦肯野细胞的树突分化均无显著影响。然而,针对这些CaMK的所有三种siRNA的组合(三基因敲低)抑制了浦肯野细胞树突的分支。此外,三基因敲低降低了浦肯野细胞中CREB的磷酸化水平。这些发现表明CaMKIIα、IIβ和IV促进了浦肯野细胞的树突分化,并且CREB磷酸化作为这些CaMK的共同底物可能参与其中。