<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-17T03:08:43Z</responseDate><request verb="GetRecord" identifier="oai:gredos.usal.es:10366/154090" metadataPrefix="edm">https://gredos.usal.es/oai/request</request><GetRecord><record><header><identifier>oai:gredos.usal.es:10366/154090</identifier><datestamp>2025-11-03T09:23:39Z</datestamp><setSpec>com_10366_4613</setSpec><setSpec>com_10366_4576</setSpec><setSpec>com_10366_3823</setSpec><setSpec>com_10366_133043</setSpec><setSpec>com_10366_3992</setSpec><setSpec>com_10366_3947</setSpec><setSpec>com_10366_3946</setSpec><setSpec>col_10366_4615</setSpec><setSpec>col_10366_135272</setSpec><setSpec>col_10366_3993</setSpec></header><metadata><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ore="http://www.openarchives.org/ore/terms/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:ds="http://dspace.org/ds/elements/1.1/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:edm="http://www.europeana.eu/schemas/edm/" xsi:schemaLocation="http://www.w3.org/1999/02/22-rdf-syntax-ns# http://www.europeana.eu/schemas/edm/EDM.xsd">
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<dc:creator>Fernández-Puente, Escarlata</dc:creator>
<dc:creator>Palomero Labajos, Jesús</dc:creator>
<dc:date>2021</dc:date>
<dc:description>[EN] Reactive oxygen and nitrogen species (RONS) play an important role in the pathophysiology of skeletal muscle and are involved in the regulation of intracellular signaling pathways,&#xd;
which drive metabolism, regeneration, and adaptation in skeletal muscle. However, the molecular&#xd;
mechanisms underlying these processes are unknown or partially uncovered. We implemented a&#xd;
combination of methodological approaches that are funded for the use of genetically encoded biosensors associated with quantitative fluorescence microscopy imaging to study redox biology in skeletal&#xd;
muscle. Therefore, it was possible to detect and monitor RONS and glutathione redox potential with&#xd;
high specificity and spatio-temporal resolution in two models, isolated skeletal muscle fibers and&#xd;
C2C12 myoblasts/myotubes. Biosensors HyPer3 and roGFP2-Orp1 were examined for the detection&#xd;
of cytosolic hydrogen peroxide; HyPer-mito and HyPer-nuc for the detection of mitochondrial and&#xd;
nuclear hydrogen peroxide; Mito-Grx1-roGFP2 and cyto-Grx1-roGFP2 were used for registration&#xd;
of the glutathione redox potential in mitochondria and cytosol. G-geNOp was proven to detect&#xd;
cytosolic nitric oxide. The fluorescence emitted by the biosensors is affected by pH, and this might&#xd;
have masked the results; therefore, environmental CO2 must be controlled to avoid pH fluctuations.&#xd;
In conclusion, genetically encoded biosensors and quantitative fluorescence microscopy provide&#xd;
a robust methodology to investigate the pathophysiological processes associated with the redox&#xd;
biology of skeletal muscle.</dc:description>
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<dc:identifier>http://hdl.handle.net/10366/154090</dc:identifier>
<dc:language>eng</dc:language>
<dc:publisher>Board</dc:publisher>
<dc:subject>2411.10 Fisiología del Músculo</dc:subject>
<dc:title>Genetically Encoded Biosensors to Monitor Intracellular Reactive Oxygen and Nitrogen Species and Glutathione Redox Potential in Skeletal Muscle Cells</dc:title>
<dc:type>info:eu-repo/semantics/article</dc:type>
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