GFP-Aequorin Protein Sensor for Ex Vivo and In Vivo Imaging of Ca2+ Dynamics in High-Ca2+ Organelles

被引:29
|
作者
Navas-Navarro, Paloma [1 ,2 ]
Rojo-Ruiz, Jonathan [1 ,2 ]
Rodriguez-Prados, Macarena [1 ,2 ]
Dolores Ganfornina, Maria [1 ,2 ]
Looger, Loren L. [3 ]
Teresa Alonso, Maria [1 ,2 ]
Garcia-Sancho, Javier [1 ,2 ]
机构
[1] Univ Valladolid, IBGM, C Sanz & Fores 3, Valladolid 47003, Spain
[2] CSIC, C Sanz & Fores 3, Valladolid 47003, Spain
[3] Howard Hughes Med Inst, Janelia Res Campus, Ashburn, VA 20147 USA
来源
CELL CHEMICAL BIOLOGY | 2016年 / 23卷 / 06期
关键词
CALCIUM; RED; ER; ACTIVATION; EXPRESSION; RELEASE; SYSTEM; CELLS;
D O I
10.1016/j.chembiol.2016.05.010
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
Proper functioning of organelles such as the ER or the Golgi apparatus requires luminal accumulation of Ca2+ at high concentrations. Here we describe a ratiometric low-affinity Ca2+ sensor of the GFPaequorin protein (GAP) family optimized for measurements in high-Ca2+ concentration environments. Transgenic animals expressing the ER-targeted sensor allowed monitoring of Ca2+ signals inside the organelle. The use of the sensor was demonstrated under three experimental paradigms: (1) ER Ca2+ oscillations in cultured astrocytes, (2) ex vivo functional mapping of cholinergic receptors triggering ER Ca2+ release in acute hippocampal slices from transgenic mice, and (3) in vivo sarcoplasmic reticulum Ca2+ dynamics in the muscle of transgenic flies. Our results provide proof of the suitability of the new biosensors to monitor Ca2+ dynamics inside intracellular organelles under physiological conditions and open an avenue to explore complex Ca2+ signaling in animal models of health and disease.
引用
收藏
页码:738 / 745
页数:8
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