The potassium channel subunit Kvβ3 interacts with pannexin 1 and attenuates its sensitivity to changes in redox potentials

被引:47
作者
Bunse, Stefanie [1 ]
Locovei, Silviu [2 ]
Schmidt, Matthias [1 ]
Qiu, Feng [2 ]
Zoidl, Georg [1 ,3 ]
Dahl, Gerhard [2 ]
Dermietzel, Rolf [1 ]
机构
[1] Ruhr Univ Bochum, Dept Neuroanat & Mol Brain Res, D-44780 Bochum, Germany
[2] Univ Miami, Sch Med, Dept Physiol & Biophys, Miami, FL USA
[3] Ruhr Univ Bochum, Dept Cytol, D-44780 Bochum, Germany
基金
美国国家卫生研究院;
关键词
channel; interacting proteins; potassium channel subunit; drug sensitivity; modulation; FUNCTIONAL-CHARACTERIZATION; SUBCELLULAR-LOCALIZATION; GAP; HEMICHANNELS; EXPRESSION; PROTEIN; FAMILY; COEXPRESSION; MODULATION; CURRENTS;
D O I
10.1111/j.1742-4658.2009.07334.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pannexin 1 (Panx1), a member of the second gap junction protein family identified in vertebrates, appears to preferentially form non-junctional membrane channels. A candidate regulatory protein of Panx1 is the potassium channel subunit Kv beta 3, previously identified by bacterial two-hybrid strategies. Here, we report on the physical association of Panx1 with Kv beta 3 by immunoprecipitation when co-expressed in a neuroblastoma cell line (Neuro2A). Furthermore, in vivo co-expression of Panx1 and Kv beta 3 was shown to occur in murine hippocampus and cerebellum. Kv beta 3 is known to accelerate inactivation of otherwise slowly inactivating potassium channels under reducing conditions. We subsequently found that Panx1 channel currents exhibit a significant reduction when exposed to reducing agents, and that this effect is attenuated in the presence of Kv beta 3. Apparently, Kv beta 3 is involved in regulating the susceptibility of Panx1 channels to redox potential. Furthermore, the Panx1 channel blockers carbenoxolone and Probenecid were less effective in inhibiting Panx1 currents when Kv beta 3 was co-expressed. The influence of Kv beta 3 on Panx1 is the first example of modulation of Panx1 channel function(s) by interacting proteins, and suggests the physiological importance of sensing changes in redox potentials.
引用
收藏
页码:6258 / 6270
页数:13
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