Grunnet Morten, Rasmussen Hannne B, Hay-Schmidt Anders, Rosenstierne Maiken, Klaerke Dan A, Olesen Søren-Peter, Jespersen Thomas
Department of Medical Physiology, The Panum Institute, University of Copenhagen, DK-2200 Copenhagen N, Denmark.
Biophys J. 2003 Sep;85(3):1525-37. doi: 10.1016/S0006-3495(03)74585-8.
Kv1 potassium channels are widely distributed in mammalian tissues and are involved in a variety of functions from controlling the firing rate of neurons to maturation of T-lymphocytes. Here we show that the newly described KCNE4 beta-subunit has a drastic inhibitory effect on currents generated by Kv1.1 and Kv1.3 potassium channels. The inhibition is found on channels expressed heterologously in both Xenopus oocytes and mammalian HEK293 cells. mKCNE4 does not inhibit Kv1.2, Kv1.4, Kv1.5, or Kv4.3 homomeric complexes, but it does significantly reduce current through Kv1.1/Kv1.2 and Kv1.2/Kv1.3 heteromeric complexes. Confocal microscopy and Western blotting reveal that Kv1.1 is present at the cell surface together with KCNE4. Real-time RT-PCR shows a relatively high presence of mKCNE4 mRNA in several organs, including uterus, kidney, lung, intestine, and in embryo, whereas a much lower mRNA level is detected in the heart and in five different parts of the brain. Having the broad distribution of Kv1 channels in mind, the demonstrated inhibitory property of KCNE4-subunits could locally and/or transiently have a dramatic influence on cellular excitability and on setting resting membrane potentials.
Kv1钾通道广泛分布于哺乳动物组织中,参与从控制神经元放电频率到T淋巴细胞成熟等多种功能。在此我们表明,新描述的KCNE4β亚基对Kv1.1和Kv1.3钾通道产生的电流具有显著抑制作用。在非洲爪蟾卵母细胞和哺乳动物HEK293细胞中异源表达的通道上均发现了这种抑制作用。mKCNE4不抑制Kv1.2、Kv1.4、Kv1.5或Kv4.3同聚体复合物,但它确实能显著降低通过Kv1.1/Kv1.2和Kv1.2/Kv1.3异聚体复合物的电流。共聚焦显微镜和蛋白质印迹显示,Kv1.1与KCNE4一起存在于细胞表面。实时逆转录聚合酶链反应显示,mKCNE4 mRNA在包括子宫、肾脏、肺、肠道和胚胎在内的多个器官中相对较高表达,而在心脏和大脑的五个不同部位检测到的mRNA水平要低得多。考虑到Kv1通道分布广泛KCNE4亚基所显示出的抑制特性可能会对细胞兴奋性和静息膜电位的设定产生局部和/或短暂的显著影响。