Mapping Calcium Dynamics in the Heart of Zebrafish Embryos with Ratiometric Genetically Encoded Calcium Indicators

• Published in: International journal of molecular sciences Vol. 21; no. 18; p. 6610
• Main Authors: Salgado-Almario, Jussep, Vicente, Manuel, Vincent, Pierre, Domingo, Beatriz, Llopis, Juan
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 10.09.2020; MDPI
• Subjects: Animals; Animals, Genetically Modified; Atria; Atrium; Binding sites; Biosensing Techniques; biosensor; Biosensors; calcium; Calcium - analysis; Calcium - metabolism; Calcium buffering; Calcium ions; Calcium signalling; Calcium-binding protein; Cardiology and cardiovascular system; Cardiomyocytes; Cardiotoxicity; Danio rerio; Drug development; Drug screening; embryo; Embryo, Nonmammalian - metabolism; Embryos; Fluorescence; Fluorescent Dyes; Genetic code; genetically encoded calcium indicator (GECI); heart; Heart function; Heart rate; Human health and pathology; Indicators; Life Sciences; Mapping; Myocardium - metabolism; Nifedipine; Physiology; Propranolol; Troponin; Troponin C; Ventricle; Vertebrates; Zebrafish; Zebrafish - genetics; Zebrafish - metabolism; genetically encoded calcium indicator (GECI); biosensor; calcium; embryo; zebrafish; imaging; heart
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms21186610

Zebrafish embryos have been proposed as a cost-effective vertebrate model to study heart function. Many fluorescent genetically encoded Ca indicators (GECIs) have been developed, but those with ratiometric readout seem more appropriate to image a moving organ such as the heart. Four ratiometric GECIs based on troponin C, TN-XXL, Twitch-1, Twitch-2B, and Twitch-4 were expressed transiently in the heart of zebrafish embryos. Their emission ratio reported the Ca levels in both the atrium and the ventricle. We measured several kinetic parameters of the Ca transients: systolic and diastolic ratio, the amplitude of the systolic Ca rise, the heart rate, as well as the rise and decay times and slopes. The systolic ratio change decreased in cells expressing high biosensor concentration, possibly caused by Ca buffering. The GECIs were able to report the effect of nifedipine and propranolol on the heart, which resulted in changes in heart rate, diastolic and systolic Ca levels, and Ca kinetics. As a result, Twitch-1 and Twitch-4 ( d 0.25 and 2.8 µM, respectively) seem the most promising GECIs for generating transgenic zebrafish lines, which could be used for modeling heart disorders, for drug screening, and for cardiotoxicity assessment during drug development.