Synaptic Structure Laboratory, Instituto de Investigación en Discapacidades Neurológicas (IDINE), Dept. Ciencias Médicas, Facultad de Medicina, Universidad Castilla-La Mancha, Campus Biosanitario, C/Almansa 14, 02008 Albacete, Spain.
Int J Mol Sci. 2020 Sep 3;21(17):6403. doi: 10.3390/ijms21176403.
The K channel interacting proteins (KChIPs) are a family of cytosolic proteins that interact with Kv4 channels, leading to higher current density, modulation of channel inactivation and faster recovery from inactivation. Using immunohistochemical techniques at the light and electron microscopic level combined with quantitative analysis, we investigated the cellular and subcellular localisation of KChIP3 and KChIP4 to compare their distribution patterns with those for Kv4.2 and Kv4.3 in the cerebellar cortex. Immunohistochemistry at the light microscopic level demonstrated that KChIP3, KChIP4, Kv4.2 and Kv4.3 proteins were widely expressed in the cerebellum, with mostly overlapping patterns. Immunoelectron microscopic techniques showed that KChIP3, KChIP4, Kv4.2 and Kv4.3 shared virtually the same somato-dendritic domains of Purkinje cells and granule cells. Application of quantitative approaches showed that KChIP3 and KChIP4 were mainly membrane-associated, but also present at cytoplasmic sites close to the plasma membrane, in dendritic spines and shafts of Purkinje cells (PCs) and dendrites of granule cells (GCs). Similarly, immunoparticles for Kv4.2 and Kv4.3 were observed along the plasma membrane and at intracellular sites in the same neuron populations. In addition to the preferential postsynaptic distribution, KChIPs and Kv4 were also distributed presynaptically in parallel fibres and mossy fibres. Immunoparticles for KChIP3, KChIP4 and Kv4.3 were detected in parallel fibres, and KChIP3, KChIP4, Kv4.2 and Kv4.3 were found in parallel fibres, indicating that composition of KChIP and Kv4 seems to be input-dependent. Together, our findings unravelled previously uncharacterised KChIP and Kv4 subcellular localisation patterns in neurons, revealed that KChIP have additional Kv4-unrelated functions in the cerebellum and support the formation of macromolecular complexes between KChIP3 and KChIP4 with heterotetrameric Kv4.2/Kv4.3 channels.
K 通道相互作用蛋白(KChIPs)是一组细胞溶质蛋白,与 Kv4 通道相互作用,导致更高的电流密度、通道失活的调节以及更快地从失活中恢复。使用光和电子显微镜水平的免疫组织化学技术结合定量分析,我们研究了 KChIP3 和 KChIP4 的细胞和亚细胞定位,以比较它们与小脑皮层中 Kv4.2 和 Kv4.3 的分布模式。光镜水平的免疫组织化学显示,KChIP3、KChIP4、Kv4.2 和 Kv4.3 蛋白在小脑广泛表达,具有大部分重叠的模式。免疫电镜技术显示,KChIP3、KChIP4、Kv4.2 和 Kv4.3 实际上共享浦肯野细胞和颗粒细胞的相同的体树突域。定量方法的应用表明,KChIP3 和 KChIP4 主要与膜相关,但也存在于靠近质膜的细胞质部位,在浦肯野细胞(PCs)的树突棘和轴突以及颗粒细胞(GCs)的树突中。同样,Kv4.2 和 Kv4.3 的免疫颗粒在同一神经元群体中沿质膜和细胞内部位观察到。除了优先的突触后分布外,KChIPs 和 Kv4 也在平行纤维和苔藓纤维中突触前分布。KChIP3、KChIP4 和 Kv4.3 的免疫颗粒在平行纤维中被检测到,KChIP3、KChIP4、Kv4.2 和 Kv4.3 被发现在平行纤维中,这表明 KChIP 和 Kv4 的组成似乎是输入依赖性的。总之,我们的发现揭示了神经元中以前未描述的 KChIP 和 Kv4 亚细胞定位模式,表明 KChIP 在小脑中有额外的与 Kv4 无关的功能,并支持 KChIP3 和 KChIP4 与异四聚体 Kv4.2/Kv4.3 通道形成大分子复合物。