Department of Physiology II, Nara Medical University, Kashihara, Nara, Japan.
Life Sci. 2012 Sep 17;91(7-8):258-63. doi: 10.1016/j.lfs.2012.07.007. Epub 2012 Jul 20.
Dorsal root ganglia contain heterogeneous populations of primary afferent neurons that transmit various sensory stimuli. This functional diversity may be correlated with differential expression of voltage-gated K(+) (Kv) channels. Here, we examine cellular distributions of Kv4 pore-forming and ancillary subunits that are responsible for fast-inactivating A-type K(+) current.
Expression pattern of Kv α-subunit, β-subunit and auxiliary subunit was investigated using immunohistochemistry, in situ hybridization and RT-PCR technique.
The two pore-forming subunits Kv4.1 and Kv4.3 show distinct cellular distributions: Kv4.3 is predominantly in small-sized C-fiber neurons, whereas Kv4.1 is seen in DRG neurons in various sizes. Furthermore, the two classes of Kv4 channel auxiliary subunits are also distributed in different-sized cells. KChIP3 is the only significantly expressed Ca(2+)-binding cytosolic ancillary subunit in DRGs and present in medium to large-sized neurons. The membrane-spanning auxiliary subunit DPP6 is seen in a large number of DRG neurons in various sizes, whereas DPP10 is restricted in small-sized neurons.
Distinct combinations of Kv4 pore-forming and auxiliary subunits may constitute A-type channels in DRG neurons with different physiological roles. Kv4.1 subunit, in combination with KChIP3 and/or DPP6, form A-type K(+) channels in medium to large-sized A-fiber DRG neurons. In contrast, Kv4.3 and DPP10 may contribute to A-type K(+) current in non-peptidergic, C-fiber somatic afferent neurons.
背根神经节包含传递各种感觉刺激的初级传入神经元的异质群体。这种功能多样性可能与电压门控钾(Kv)通道的差异表达有关。在这里,我们研究了负责快速失活 A 型 K(+)电流的 Kv4 孔形成亚基和辅助亚基的细胞分布。
使用免疫组织化学、原位杂交和 RT-PCR 技术研究 Kv α-亚基、β-亚基和辅助亚基的表达模式。
两个孔形成亚基 Kv4.1 和 Kv4.3 表现出不同的细胞分布:Kv4.3 主要存在于小尺寸 C 纤维神经元中,而 Kv4.1 存在于各种大小的背根神经节神经元中。此外,两类 Kv4 通道辅助亚基也分布在不同大小的细胞中。KChIP3 是背根神经节中唯一显著表达的 Ca(2+)结合胞质辅助亚基,存在于中到大神经元中。膜跨膜辅助亚基 DPP6 存在于各种大小的大量背根神经节神经元中,而 DPP10 则局限于小尺寸神经元中。
不同的 Kv4 孔形成亚基和辅助亚基的组合可能在具有不同生理作用的背根神经节神经元中构成 A 型通道。Kv4.1 亚基与 KChIP3 和/或 DPP6 结合,形成中到大 A 纤维背根神经节神经元中的 A 型 K(+)通道。相比之下,Kv4.3 和 DPP10 可能有助于非肽能、C 纤维躯体传入神经元中的 A 型 K(+)电流。