Modulation of Mammary Stromal Cell Lactate Dynamics by Ambient Glucose and Epithelial Factors
Author
dc.contributor.author
Tobar Bachler, Nicolás
Author
dc.contributor.author
Porras Espinoza, Omar
Author
dc.contributor.author
Smith, Patricio C.
Author
dc.contributor.author
Barros, L. Felipe
Author
dc.contributor.author
Martínez, Jorge
Admission date
dc.date.accessioned
2019-05-29T13:59:12Z
Available date
dc.date.available
2019-05-29T13:59:12Z
Publication date
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2017
Cita de ítem
dc.identifier.citation
Journal of Cellular Physiology, 232: 136–144, 2017
Identifier
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10974652
Identifier
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00219541
Identifier
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10.1002/jcp.25398
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/169169
Abstract
dc.description.abstract
Hyperglycemia is a risk factor for a variety of human cancers. Increased access to glucose and that tumor metabolize glucose by a glycolyticprocess even in the presence of oxygen (Warburg effect), provide a framework to analyze a particular set of metabolic adaptationmechanisms that may explain this phenomenon. In the present work, using a mammary stromal cell line derived from healthy tissue that wassubjected to a long-term culture in low (5 mM) or high (25 mM) glucose, we analyzed kinetic parameters of lactate transport using a FRETbiosensor. Our results indicate that the glucose pre-culture and soluble epithelial factors constitute a stimulus for lactate stromalproduction, factors that also modify the kinetic parameters and the monocarboxylate transporters expression in stromal cells. We alsoobserved a vectorialflux of lactate from stroma to epithelial cells in a co-culture setting and found that the uptake of lactate by epithelialcells correlates with the degree of malignancy. Glucose preconditioning of the stromal cell stimulated epithelial motility. Ourfindingssuggest that lactate generated by stromal cells in the high glucose condition stimulate epithelial migration. Overall, our results support thenotion that glucose not only provides a substrate for tumor nutrition but also behaves as a signal promoting malignancy.