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dc.contributor.authorBurgos, Paulina
dc.contributor.authorZúñiga, Rafael
dc.contributor.authorDomínguez, Pedro
dc.contributor.authorDelgado-López, Fernando
dc.contributor.authorPlant, Leigh D.
dc.contributor.authorZúñiga, Leandro
dc.date.accessioned2017-11-13T12:20:19Z
dc.date.available2017-11-13T12:20:19Z
dc.date.issued2014
dc.identifier.urihttp://repositorio.ucm.cl/handle/ucm/1185
dc.description.abstractTwo pore domain potassium (K2P) channels are mostly present in the central nervous system (CNS) where they play important roles in modulating neuronal excitability. K2P channels give rise to background K+ currents (IKSO) a key component in setting and maintaining the resting membrane potential in excitable cells. Here, we studied the expression and relative abundances of K2P channels in cerebellar granule neurons (CGNs), combining molecular biology, electrophysiology and immunologic techniques. The CGN IKSO was very sensitive to external pH, as previously reported. Quantitative determination of mRNA expression level demonstrated the existence of an accumulation pattern of transcripts in CGN that encode K2P9 > K2P1 > K2P3 > K2P18 > K2P2 = K2P10 > K2P4 > K2P5 subunits. The presence of the major K2P subunits expressed was then confirmed by Western blot and immunofluorescence analysis, demonstrating robust expression of K2P1 (TWIK-1), K2P3 (TASK-1), K2P9 (TASK-3) and K2P18 (TRESK) channel protein. Based, on these results, it is concluded that K2P1, -3, -9 and -18 subunits represent the majority component of IKSO current in CGN.es_CL
dc.language.isoenes_CL
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
dc.sourceBiochemical and Biophysical Research Communications, 453(4), 754-760es_CL
dc.subjectK2P channelses_CL
dc.subjectTwo-pore domain potassium channelses_CL
dc.subjectCerebellar granule neurons (CGNs)es_CL
dc.titleDifferential expression of two-pore domain potassium channels in rat cerebellar granule neuronses_CL
dc.typeArticlees_CL
dc.ucm.facultadFacultad de Medicinaes_CL
dc.ucm.indexacionScopuses_CL
dc.ucm.indexacionIsies_CL
dc.ucm.urisibib2.ucm.cl:2048/login?url=https://www.sciencedirect.com/science/article/pii/S0006291X14017999?via%3Dihubes_CL
dc.ucm.doidoi.org/10.1016/j.bbrc.2014.10.012es_CL


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Atribución-NoComercial-SinDerivadas 3.0 Chile
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