Compartir
Título
Expression and functional analysis of the hydrogen peroxide biosensors HyPer and HyPer2 in C2C12 myoblasts/myotubes and single skeletal muscle fibres
Autor(es)
Palabras clave
Muscle
Skeletal muscle fibres
HyPer
Hydrogen peroxide
Clasificación UNESCO
2411.10 Fisiología del Músculo
Fecha de publicación
2020
Editor
Springer
Citación
Fernández Puente, E., Sánchez Martín, M.A., Andrés, J., Rodríguez Izquierdo, L., Méndez, L., Palomero Labajos, J. (2020). Expression and functional analysis of the hydrogen peroxide biosensors HyPer and HyPer2 in C2C12 myoblasts/myotubes and single skeletal muscle fibres. Scientific Reports, 10 (1) pp 1-15. https://doi.org/10.1038/s41598-020-57821-1
Resumen
[EN] Hydrogen peroxide (H2O2) is generated in cells and plays an important role as a signalling molecule. It
has been reported that H2O2 is involved in physiological and pathological processes in skeletal muscle.
However, H2O2 detection in cells with traditional techniques produces frequent artefacts. Currently,
the HyPer biosensor detects intracellular H2O2 specifcally in real time using fuorescence microscopy.
The aim of this study was to develop and optimize approaches used to express the HyPer biosensor
in diferent models of skeletal muscle cells, such as the C2C12 myoblast/myotube cell line and mature
skeletal muscle fbres isolated from C57BL/6J mice, and to measure intracellular H2O2 in real time
in these cells. The results show that the expression of the HyPer biosensor in skeletal muscle cells is
possible. In addition, we demonstrate that HyPer is functional and that this biosensor detects changes
and fuctuations in intracellular H2O2 in a reversible manner. The HyPer2 biosensor, which is a more
advanced version of HyPer, presents improved properties in terms of sensitivity in detecting lower
concentrations of H2O2 in skeletal muscle fbres. In conclusion, the expression of the HyPer biosensor
in the diferent experimental models combined with fuorescence microscopy techniques is a powerful
methodology to monitor and register intracellular H2O2 specifcally in skeletal muscle. The innovation of
the methodological approaches presented in this study may present new avenues for studying the role
of H2O2 in skeletal muscle pathophysiology. Furthermore, the methodology may potentially be adapted
to yield other specifc biosensors for diferent reactive oxygen and nitrogen species or metabolites
involved in cellular functions.
URI
DOI
10.1038/S41598-020-57821-1
Versión del editor
Aparece en las colecciones
Fichier(s) constituant ce document
Tamaño:
2.071Mo
Formato:
Adobe PDF













