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Methods Mol Biol ; 2816: 69-75, 2024.
Article in English | MEDLINE | ID: mdl-38977589

ABSTRACT

Intracellular Ca2+ can be conveniently monitored by sensitive Ca2+ fluorescent dyes in live cells. The Gαq involved lipid signaling pathways and, thus, can be studied by intracellular Ca2+ imaging. Here we describe the protocols to measure intracellular Ca2+ for studying PEG2-EP1 activity in esophageal smooth muscle cells. The ratiometric Fura-2 imaging provides quantitative data, and the Fluo-4 confocal microscopic imaging has high-spatial resolution.


Subject(s)
Calcium , Receptors, G-Protein-Coupled , Calcium/metabolism , Receptors, G-Protein-Coupled/metabolism , Animals , Microscopy, Confocal/methods , Signal Transduction , Myocytes, Smooth Muscle/metabolism , Calcium Signaling , Humans , Xanthenes/metabolism , Fura-2/metabolism , Lipid Metabolism , Esophagus/metabolism , Fluorescent Dyes/chemistry , Fluorescent Dyes/metabolism , Aniline Compounds
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