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dc.contributorUniversitat Ramon Llull. IQS
dc.contributor.authorMartínez-Monge, Iván
dc.contributor.authorAlbiol, Joan
dc.contributor.authorLecina i Veciana, Martí
dc.contributor.authorListe Calleja, Leticia
dc.contributor.authorMiret, Joan
dc.contributor.authorSolà, Carles
dc.contributor.authorCairó, Jordi Joan
dc.date.accessioned2024-02-08T13:28:16Z
dc.date.available2024-02-08T13:28:16Z
dc.date.issued2018-10-26
dc.identifier.issn1097-0290ca
dc.identifier.urihttp://hdl.handle.net/20.500.14342/3904
dc.description.abstractAt early stages of the exponential growth phase in HEK293 cell cultures, the tricarboxylic acid cycle is unable to process all the amount of NADH generated in the glycolysis pathway, being lactate the main by-product. However, HEK293 cells are also able to metabolize lactate depending on the environmental conditions. It has been recently observed that one of the most important modes of lactate metabolization is the cometabolism of lactate and glucose, observed even during the exponential growth phase. Extracellular lactate concentration and pH appear to be the key factors triggering the metabolic shift from glucose consumption and lactate production to lactate and glucose concomitant consumption. The hypothesis proposed for triggering this metabolic shift to lactate and glucose concomitant consumption is that HEK293 cells metabolize extracellular lactate as a response to both extracellular protons and lactate accumulation, by means of cotransporting them (extracellular protons and lactate) into the cytosol. At this point, there exists a considerable controversy about how lactate reaches the mitochondrial matrix: the first hypothesis proposes that lactate is converted into pyruvate in the cytosol, and afterward, pyruvate enters into the mitochondria; the second alternative considers that lactate enters first into the mitochondria, and then, is converted into pyruvate. In this study, lactate transport and metabolization into mitochondria is shown to be feasible, as evidenced by means of respirometry tests with isolated active mitochondria, including the depletion of lactate concentration of the respirometry assay. Although the capability of lactate metabolization by isolated mitochondria is demonstrated, the possibility of lactate being converted into pyruvate in the cytosol cannot be excluded from the discussion. For this reason, the calculation of the metabolic fluxes for an HEK293 cell line was performed for the different metabolic phases observed in batch cultures under pH controlled and noncontrolled conditions, considering both hypotheses. The main objective of this study is to evaluate the redistribution of cellular metabolism and compare the differences or similarities between the phases before and after the metabolic shift of HEK293 cells (shift observed when pH is not controlled). That is from a glucose consumption/lactate production phase to a glucose-lactate coconsumption phase. Interestingly, switching to a glucose and lactate cometabolization results in a better-balanced cell metabolism, with decreased glucose and amino acids uptake rates, affecting minimally cell growth. This behavior could be applied to further develop new approaches in terms of cell engineering and to develop improved cell culture strategies in the field of animal cell technology.ca
dc.format.extent17 p.ca
dc.language.isoengca
dc.publisherWileyca
dc.relation.ispartofBiotechnology and Bioengineeringca
dc.rights© Wileyca
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.otherCometabolism of glucose and lactateca
dc.subject.otherHEK293ca
dc.subject.otherMetabolic flux analysisca
dc.subject.otherMetabolic shiftca
dc.subject.otherMetabolismeca
dc.titleMetabolic flux balance analysis during lactate and glucose concomitant consumption in HEK293 cell culturesca
dc.typeinfo:eu-repo/semantics/articleca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.terms12 mesosca
dc.subject.udc612ca
dc.identifier.doihttps://doi.org/10.1002/bit.26858ca
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/PN I+D/BIO2012–32151ca
dc.relation.projectIDinfo:eu-repo/grantAgreement/SUR del DEC/FI-DGRca
dc.description.versioninfo:eu-repo/semantics/acceptedVersionca


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