Ca2+ channel nanodomains boost local Ca2+ amplitude

被引:62
作者
Tadross, Michael R. [1 ,2 ,3 ]
Tsien, Richard W. [2 ,4 ]
Yue, David T. [3 ,5 ]
机构
[1] Howard Hughes Med Inst, Ashburn, VA 20147 USA
[2] Stanford Univ, Beckman Ctr, Sch Med, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
[3] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Calcium Signals Lab, Baltimore, MD 21205 USA
[4] NYU, Langone Med Ctr, Neurosci Inst, New York, NY 10016 USA
[5] Johns Hopkins Univ, Sch Med, Dept Neurosci, Calcium Signals Lab, Baltimore, MD 21205 USA
关键词
signaling; uncaging; biosensor; electrodiffusion; SACCULAR HAIR-CELLS; CALCIUM-CHANNEL; CA2+-DEPENDENT INACTIVATION; NEUROTRANSMITTER RELEASE; DIFFUSION-COEFFICIENT; VENTRICULAR MYOCYTES; SYNAPTIC PLASTICITY; TRANSMITTER RELEASE; CA(V)1.3 CHANNELS; GLUTAMATE RELEASE;
D O I
10.1073/pnas.1313898110
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
Local Ca2+ signals through voltage-gated Ca2+ channels (Ca(V)s) drive synaptic transmission, neural plasticity, and cardiac contraction. Despite the importance of these events, the fundamental relationship between flux through a single Ca-V channel and the Ca2+ signaling concentration within nanometers of its pore has resisted empirical determination, owing to limitations in the spatial resolution and specificity of fluorescence-based Ca2+ measurements. Here, we exploited Ca2+-dependent inactivation of Ca-V channels as a nanometer-range Ca2+ indicator specific to active channels. We observed an unexpected and dramatic boost in nanodomain Ca2+ amplitude, ten-fold higher than predicted on theoretical grounds. Our results uncover a striking feature of Ca-V nanodomains, as diffusion-restricted environments that amplify small Ca2+ fluxes into enormous local Ca2+ concentrations. This Ca2+ tuning by the physical composition of the nanodomain may represent an energy-efficient means of local amplification that maximizes information signaling capacity, while minimizing global Ca2+ load.
引用
收藏
页码:15794 / 15799
页数:6
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