Visualizing sodium dynamics in isolated cardiomyocytes using fluorescent nanosensors

被引:56
作者
Dubach, J. Matthew [1 ]
Das, Saumya [2 ,3 ]
Rosenzweig, Anthony [2 ]
Clark, Heather A. [1 ]
机构
[1] Charles Stark Draper Lab, Biomed Engn Grp, Cambridge, MA 02139 USA
[2] Beth Israel Deaconess Med Ctr, Cardiovasc Inst, Boston, MA 02215 USA
[3] Massachusetts Gen Hosp, Div Cardiovasc, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
cellular imaging; ion channels; sodium sparks; CARDIAC MYOCYTES; VENTRICULAR MYOCYTES; CHANNELS; CELLS; RECEPTOR; SCN9A; RAT; NA+; STIMULATION; INHIBITION;
D O I
10.1073/pnas.0905909106
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
Regulation of sodium flux across the cell membrane plays a vital role in the generation of action potentials and regulation of membrane excitability in cells such as cardiomyocytes and neurons. Alteration of sodium channel function has been implicated in diseases such as epilepsy, long QT syndrome, and heart failure. However, single cell imaging of sodium dynamics has been limited due to the narrow selection of fluorescent sodium indicators available to researchers. Here we report, the detection of spatially defined sodium activity during action potentials. Fluorescent nanosensors that measure sodium in real-time, are reversible and are completely selective over other cations such as potassium that were used to image sodium. The use of the nanosensors in vitro was validated by determining drug-induced activation in heterologous cells transfected with the voltage-gated sodium channel Na(V)1.7. Spatial information of sodium concentrations during action potentials will provide insight at the cellular level on the role of sodium and how slight changes in sodium channel function can affect the entirety of an action potential.
引用
收藏
页码:16145 / 16150
页数:6
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