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Feasibility of simultaneous measurement of cytosolic calcium and hydrogen peroxide in vascular smooth muscle cells

Interplay between calcium ions (Ca(2+)) and reactive oxygen species (ROS) delicately controls diverse pathophysiological functions of vascular smooth muscle cells (VSMCs). However, details of the Ca(2+) and ROS signaling network have been hindered by the absence of a method for dual measurement of C...

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Detalles Bibliográficos
Autores principales: Chang, Kyung-Hwa, Park, Jung-Min, Lee, Moo-Yeol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4133858/
https://www.ncbi.nlm.nih.gov/pubmed/24195793
http://dx.doi.org/10.5483/BMBRep.2013.46.12.103
Descripción
Sumario:Interplay between calcium ions (Ca(2+)) and reactive oxygen species (ROS) delicately controls diverse pathophysiological functions of vascular smooth muscle cells (VSMCs). However, details of the Ca(2+) and ROS signaling network have been hindered by the absence of a method for dual measurement of Ca(2+) and ROS. Here, a real-time monitoring system for Ca(2+) and ROS was established using a genetically encoded hydrogen peroxide indicator, HyPer, and a ratiometric Ca(2+) indicator, fura-2. For the simultaneous detection of fura-2 and HyPer signals, 540 nm emission filter and 500 nm∼ dichroic beamsplitter were combined with conventional exciters. The wide excitation spectrum of HyPer resulted in marginal cross-contamination with fura-2 signal. However, physiological Ca(2+) transient and hydrogen peroxide were practically measurable in HyPer-expressing, fura-2-loaded VSMCs. Indeed, distinct Ca(2+) and ROS signals could be successfully detected in serotonin-stimulated VSMCs. The system established in this study is applicable to studies of crosstalk between Ca(2+) and ROS. [BMB Reports 2013; 46(12): 600-605]