FGF14 is a regulator of KCNQ2/3 channels

被引:39
|
作者
Pablo, Juan Lorenzo [1 ,2 ]
Pitt, Geoffrey S. [1 ,2 ,3 ,4 ]
机构
[1] Duke Univ, Med Ctr, Dept Neurobiol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Ion Channel Res Unit, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Med, Div Cardiol, Durham, NC 27710 USA
[4] Weill Cornell Med, Cardiovasc Res Inst, New York, NY 10021 USA
关键词
FGF14; KCNQ2; fibroblast growth factor homologous factors; axon initial segment; ankyrin-G; VOLTAGE-GATED SODIUM; AXON INITIAL SEGMENT; FACTOR HOMOLOGOUS FACTORS; NEURONAL EXCITABILITY; POTASSIUM CHANNELS; NA+ CHANNELS; ANKYRIN-G; FIBROBLAST-GROWTH-FACTOR-14; GENE; CRYSTAL-STRUCTURE; K+ CHANNELS;
D O I
10.1073/pnas.1610158114
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
KCNQ2/3 (Kv7.2/7.3) channels and voltage-gated sodium channels (VGSCs) are enriched in the axon initial segment (AIS) where they bind to ankyrin-G and coregulate membrane potential in central nervous system neurons. The molecular mechanisms supporting coordinated regulation of KCNQ and VGSCs and the cellular mechanisms governing KCNQ trafficking to the AIS are incompletely understood. Here, we show that fibroblast growth factor 14 (FGF14), previously described as a VGSC regulator, also affects KCNQ function and localization. FGF14 knockdown leads to a reduction of KCNQ2 in the AIS and a reduction in whole-cell KCNQ currents. FGF14 positively regulates KCNQ2/3 channels in a simplified expression system. FGF14 interacts with KCNQ2 at a site distinct from the FGF14-VGSC interaction surface, thus enabling the bridging of Na(V)1.6 and KCNQ2. These data implicate FGF14 as an organizer of channel localization in the AIS and provide insight into the coordination of KCNQ and VGSC conductances in the regulation of membrane potential.
引用
收藏
页码:154 / 159
页数:6
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