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dc.contributor.author Contreras-Baeza, Yasna
dc.contributor.author Sandoval, Pamela Y.
dc.contributor.author Alarcón, Romina
dc.contributor.author Galaz, Alex
dc.contributor.author Cortés-Molina, Francisca
dc.contributor.author Alegriá, Karin
dc.contributor.author Baeza-Lehnert, Felipe
dc.contributor.author Arce-Molina, Robinson
dc.contributor.author Guequén, Anita
dc.contributor.author Flores, Carlos A.
dc.contributor.author Martín, Alejandro San
dc.contributor.author Barros, L. Felipe
dc.date.accessioned 2024-09-26T00:34:23Z
dc.date.available 2024-09-26T00:34:23Z
dc.date.issued 2019-12-27
dc.identifier.issn 0021-9258
dc.identifier.uri https://repositorio.uss.cl/handle/uss/12658
dc.description Funding Information: Acknowledgments—We thank Karen Everett for critical reading of the manuscript and José Sarmiento (Universidad Austral de Chile) for help with confocal microscopy of MCT4 in human macrophages. We thank Drs. Brandon Faubert and Ralph J. DeBerardinis (Children’s Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, TX) for a generous gift of the MCT4-Lenti-CRISPR_V2 construct. The Centro de Estudios Científicos (CECs) is funded by the Chilean Government through the Centers of Excellence Basal Financing Program of CONICYT. Funding Information: This work was supported by Fondecyt Grants 11150930 (to A. S. M.), 1160317 (to L. F. B.), and 11190584 (to P. Y. S.). The authors declare that they have no conflicts of interest with the contents of this article. Publisher Copyright: © 2019 Contreras-Baeza et al. Published by The American Society for Biochemistry and Molecular Biology, Inc.
dc.description.abstract Monocarboxylate transporter 4 (MCT4) is an H-coupled symporter highly expressed in metastatic tumors and at inflammatory sites undergoing hypoxia or the Warburg effect. At these sites, extracellular lactate contributes to malignancy and immune response evasion. Intriguingly, at 30-40 mM, the reported Km of MCT4 for lactate is more than 1 order of magnitude higher than physiological or even pathological lactate levels. MCT4 is not thought to transport pyruvate. Here we have characterized cell lactate and pyruvate dynamics using the FRET sensors Laconic and Pyronic. Dominant MCT4 permeability was demonstrated in various cell types by pharmacological means and by CRISPR/Cas9-mediated deletion. Respective Km values for lactate uptake were 1.7, 1.2, and 0.7mM in MDA-MB-231 cells, macrophages, and HEK293 cells expressing recombinant MCT4. In MDA-MB-231 cells MCT4 exhibited a Km for pyruvate of 4.2mM, as opposed to>150mMreported previously. Parallel assays with the pH-sensitive dye 2-,7-bis-(carboxyethyl)-5-(and-6)-carboxyfluorescein (BCECF) indicated that previous Km estimates based on substrate-induced acidification were severely biased by confounding pH-regulatory mechanisms. Numerical simulation using revised kinetic parameters revealed that MCT4, but not the related transportersMCT1and MCT2, endows cells with the ability to export lactate in highlactate microenvironments. In conclusion, MCT4 is a high-affinity lactate transporter with physiologically relevant affinity for pyruvate. en
dc.language.iso eng
dc.relation.ispartof vol. 294 Issue: no. 52 Pages: 20135-20147
dc.source Journal of Biological Chemistry
dc.title Monocarboxylate transporter 4 (MCT4) is a high affinity transporter capable of exporting lactate in high-lactate microenvironments en
dc.type Artículo
dc.identifier.doi 10.1074/jbc.RA119.009093


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