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dc.contributor.authorPittolo, Silviaes_ES
dc.contributor.authorLee, Hyojunges_ES
dc.contributor.authorLladó, Annaes_ES
dc.contributor.authorTosi, Sébastienes_ES
dc.contributor.authorBosch, Miqueles_ES
dc.contributor.authorBardia, Lídiaes_ES
dc.contributor.authorGómez-Santacana, Xavieres_ES
dc.contributor.authorLlebaria, Amadeues_ES
dc.contributor.authorSoriano, Eduardoes_ES
dc.contributor.authorColombelli, Julienes_ES
dc.contributor.authorPoskanzer, Kira E.es_ES
dc.contributor.authorPerea, Gertrudises_ES
dc.contributor.authorGorostiza, Paues_ES
dc.date.accessioned2020-02-14T11:05:06Z-
dc.date.available2020-02-14T11:05:06Z-
dc.date.issued2019-07-02-
dc.identifier.citationProceedings of the National Academy of Sciences of the United States of America 116 (27): 13680-13689 (2019)es_ES
dc.identifier.urihttp://hdl.handle.net/10261/200686-
dc.description.abstractThe physiological activity of proteins is often studied with loss-of-function genetic approaches, but the corresponding phenotypes develop slowly and can be confounding. Photopharmacology allows direct, fast, and reversible control of endogenous protein activity, with spatiotemporal resolution set by the illumination method. Here, we combine a photoswitchable allosteric modulator (alloswitch) and 2-photon excitation using pulsed near-infrared lasers to reversibly silence metabotropic glutamate 5 (mGlu5) receptor activity in intact brain tissue. Endogenous receptors can be photoactivated in neurons and astrocytes with pharmacological selectivity and with an axial resolution between 5 and 10 μm. Thus, 2-photon pharmacology using alloswitch allows investigating mGlu5-dependent processes in wild-type animals, including synaptic formation and plasticity, and signaling pathways from intracellular organelles. © 2019 National Academy of Sciences. All rights reserved.es_ES
dc.description.sponsorshipACKNOWLEDGMENTS. We thank Jordi Hernando (Autonomous University of Barcelona) for useful discussions on 2-photon excitation; Pere Català (Utrecht University) for help with GCaMP; Francisco Ciruela (University of Barcelona) for mGlu5-eYFP plasmid; Erin Schuman and Stephan Junek (Max Planck Institute for Brain Research, Frankfurt) for preliminary 2-photon excitation experiments; and Ashraf Muhaisen (University of Barcelona) for help with slicing. This research received funding from European Union Research and Innovation Programme Horizon 2020 [Human Brain Project SGA2 Grant Agreement 785907 (WaveScalES)], European Research ERA-Net SynBio programme (Modulightor project), and financial support from Agency for Management of University and Research Grants/Generalitat de Catalunya (CERCA Programme; 2017-SGR-1442 project), Fonds Européen de Développement Économique et Régional (FEDER) funds, Ministry of Economy and Competitiveness (MINECO)/FEDER (Grant CTQ2016-80066-R), and the Fundaluce foundation. S.P. was supported by an FI fellowship from the Agency for Management of University and Research Grants/Generalitat de Catalunya (2014FI_B2 00160). H.L. was supported by an Institute for Bioengineering of Catalonia Severo Ochoa International PhD Programme fellowship from MINECO. M.B. was supported by a H2020-MSCA-IF Reintegration Grant. K.E.P. receives support from NIH/National Institute of Neurological Disorders and Stroke Grant R01NS099254 and NSF Biophotonics Grant 1604544. E.S. receives support from MINECO (Grant SAF2016-7426).es_ES
dc.language.isoenges_ES
dc.publisherNational Academy of Sciences (U.S.)es_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/785907es_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2016-80066-Res_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/SAF2016-7426-Res_ES
dc.relation.isversionofPublisher's versiones_ES
dc.rightsopenAccesses_ES
dc.subject2-photon pharmacologyes_ES
dc.subjectFunctional silencinges_ES
dc.subjectPharmacological selectivityes_ES
dc.subjectPhotoactivationes_ES
dc.subjectPhotopharmacologyes_ES
dc.titleReversible silencing of endogenous receptors in intact brain tissue using 2-photon pharmacologyes_ES
dc.typeartículoes_ES
dc.identifier.doi10.1073/pnas.1900430116-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1073/pnas.1900430116es_ES
dc.contributor.funderEuropean Commissiones_ES
dc.contributor.funderMinisterio de Economía y Competitividad (España)es_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.contributor.orcidLlebaría, Amadeu [0000-0002-8200-4827]es_ES
dc.identifier.pmid31196955-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.openairetypeartículo-
item.fulltextWith Fulltext-
item.languageiso639-1en-
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