Pharmakologisches Institut, BPC-Marburg, Fachbereich Medizin, Philipps-Universität Marburg, Karl-von-Frisch-Straße 2, 35043 Marburg, Germany.
Walther-Straub-Institut für Pharmakologie und Toxikologie, Ludwig-Maximilians-Universität München, 80336 München, Germany.
Cells. 2020 Feb 18;9(2):459. doi: 10.3390/cells9020459.
The cation channel subunit TRPC1 is strongly expressed in central neurons including neurons in the CA1 region of the hippocampus where it forms complexes with TRPC4 and TRPC5. To investigate the functional role of TRPC1 in these neurons and in channel function, we compared current responses to group I metabotropic glutamate receptor (mGluR I) activation and looked for major differences in dendritic morphology in neurons from and mice. mGluR I stimulation resulted in the activation of a voltage-dependent nonselective cation current in both genotypes. Deletion of TRPC1 resulted in a modification of the shape of the current-voltage relationship, leading to an inward current increase. In current clamp recordings, the percentage of neurons that responded to depolarization in the presence of an mGluR I agonist with a plateau potential was increased in mice. There was also a small increase in the minor population of CA1 neurons that have more than one apical dendrite in mice. We conclude that TRPC1 has an inhibitory effect on receptor-operated nonselective cation channels in hippocampal CA1 neurons probably as a result of heterotetramer formation with other TRPC isoforms, and that TRPC1 deletion has only minor effects on dendritic morphology.
阳离子通道亚基 TRPC1 在中枢神经元中表达强烈,包括海马 CA1 区的神经元,在那里它与 TRPC4 和 TRPC5 形成复合物。为了研究 TRPC1 在这些神经元中的功能作用和通道功能,我们比较了对 I 组代谢型谷氨酸受体(mGluR I)激活的电流反应,并寻找 和 小鼠神经元树突形态的主要差异。mGluR I 刺激导致两种基因型中都激活了电压依赖性非选择性阳离子电流。TRPC1 的缺失导致电流-电压关系的形状发生改变,导致内向电流增加。在电流钳记录中,在存在 mGluR I 激动剂的情况下,用平台电位对去极化作出反应的神经元百分比在 小鼠中增加。在 小鼠中,具有一个以上顶树突的 CA1 神经元的次要群体也略有增加。我们得出结论,TRPC1 对海马 CA1 神经元中的受体操纵非选择性阳离子通道具有抑制作用,可能是由于与其他 TRPC 亚型形成异四聚体的结果,并且 TRPC1 的缺失对树突形态只有微小的影响。