Real-Time Intracellular Mg2+ Signaling and Wave Propagation by Subdiffraction-Limit Super-Resolution Microscopy

被引:1
作者
Chakkarapani, Suresh Kumar [1 ]
Lee, Seungah [2 ,3 ]
Lee, Gwang [4 ,5 ]
Kang, Seong Ho [1 ,2 ,3 ]
机构
[1] Kyung Hee Univ, Grad Sch, Dept Chem, Yongin 446701, South Korea
[2] Kyung Hee Univ, Dept Appl Chem, Yongin 446701, South Korea
[3] Kyung Hee Univ, Inst Nat Sci, Yongin 446701, South Korea
[4] Ajou Univ, Sch Med, Dept Physiol, Suwon 443749, South Korea
[5] Ajou Univ, Sch Med, Dept Biomed Sci, Suwon 443749, South Korea
来源
BULLETIN OF THE KOREAN CHEMICAL SOCIETY | 2015年 / 36卷 / 11期
基金
新加坡国家研究基金会;
关键词
dSTORM; High temporal resolution; Intracellular Mg2+; Single-cell analysis; Super-resolution imaging; FLUORESCENT INDICATOR; VENTRICULAR MYOCYTES; MODULATION; MAGNESIUM; HOMEOSTASIS; CHELATORS; CHANNELS; CA-2+;
D O I
10.1002/bkcs.10521
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Magnesium ion (Mg2+) is an important intracellular component that plays a fundamental role in many cellular processes. The super-localization of intracellular Mg2+ signaling and wave propagation in a single cell with subdiffraction-limit image resolution is demonstrated for the first time by direct stochastic optical reconstruction microscopy (dSTORM). Mag-fluo-4-AM, an intracellular Mg2+ fluorescent indicator dye, is used for the fluorescence imaging of intracellular Mg2+ in human embryonic kidney 293 (HEK-293) cells as a model. Mag-fluo-4-AM is photoswitched between its fluorescent and dark states and the resulting super-resolution cell image reveals uniform and specific labeling of Mg2+ with thousands of fluorophores per cell and localization precision of 21 +/- 1nm. Furthermore, the real-time dynamics of Mg2+ wave propagation are studied by dSTORM. The sparks and waves show random temporal propagation patterns in nonhomogeneous substructures with 0.2s time intervals. Thus, dSTORM allows characterization of intracellular processes at sub-nanometre spatial resolution with high temporal resolution.
引用
收藏
页码:2589 / 2595
页数:7
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