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dc.contributor.author Medel, Vicente
dc.contributor.author Crossley, Nicolás
dc.contributor.author Gajardo, Ivana
dc.contributor.author Muller, Eli
dc.contributor.author Barros, L. Felipe
dc.contributor.author Shine, James M.
dc.contributor.author Sierralta, Jimena
dc.date.accessioned 2024-09-26T00:34:12Z
dc.date.available 2024-09-26T00:34:12Z
dc.date.issued 2022-08-16
dc.identifier.issn 0027-8424
dc.identifier.uri https://repositorio.uss.cl/handle/uss/12645
dc.description Publisher Copyright: Copyright © 2022 the Author(s). Published by PNAS.
dc.description.abstract Brain activity is constrained by local availability of chemical energy, which is generated through compartmentalized metabolic processes. By analyzing data of whole human brain gene expression, we characterize the spatial distribution of seven glucose and monocarboxylate membrane transporters that mediate astrocyte–neuron lactate shuttle transfer of energy. We found that the gene coding for neuronal MCT2 is the only gene enriched in cerebral cortex where its abundance is inversely correlated with cortical thickness. Coexpression network analysis revealed that MCT2 was the only gene participating in an organized gene cluster enriched in K+ dynamics. Indeed, the expression of KATP subunits, which mediate lactate increases with spiking activity, is spatially coupled to MCT2 distribution. Notably, MCT2 expression correlated with fluorodeoxyglucose positron emission tomography task-dependent glucose utilization. Finally, the MCT2 messenger RNA gradient closely overlaps with functional MRI brain regions associated with attention, arousal, and stress. Our results highlight neuronal MCT2 lactate transporter as a key component of the cross-talk between astrocytes and neurons and a link between metabolism, cortical structure, and state-dependent brain function. en
dc.language.iso eng
dc.relation.ispartof vol. 119 Issue: no. 33 Pages:
dc.source Proceedings of the National Academy of Sciences of the United States of America
dc.title Whole-brain neuronal MCT2 lactate transporter expression links metabolism to human brain structure and function en
dc.type Artículo
dc.identifier.doi 10.1073/pnas.2204619119
dc.publisher.department Facultad de Medicina y Ciencia


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