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Tissue-resident NK cells differ in their expression profile of the nutrient transporters Glut1, CD98 and CD71

Metabolism is a critical basis for immune cell functionality. It was recently shown that NK cell subsets from peripheral blood modulate their expression of nutrient receptors following cytokine stimulation, demonstrating that NK cells can adjust to changes in metabolic requirements. As nutrient avai...

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Autores principales: Salzberger, Wilhelm, Martrus, Gloria, Bachmann, Kai, Goebels, Hanna, Heß, Leonard, Koch, Martina, Langeneckert, Annika, Lunemann, Sebastian, Oldhafer, Karl J., Pfeifer, Caroline, Poch, Tobias, Richert, Laura, Schramm, Christoph, Wahib, Ramez, Bunders, Madeleine J., Altfeld, Marcus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054388/
https://www.ncbi.nlm.nih.gov/pubmed/30028872
http://dx.doi.org/10.1371/journal.pone.0201170
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author Salzberger, Wilhelm
Martrus, Gloria
Bachmann, Kai
Goebels, Hanna
Heß, Leonard
Koch, Martina
Langeneckert, Annika
Lunemann, Sebastian
Oldhafer, Karl J.
Pfeifer, Caroline
Poch, Tobias
Richert, Laura
Schramm, Christoph
Wahib, Ramez
Bunders, Madeleine J.
Altfeld, Marcus
author_facet Salzberger, Wilhelm
Martrus, Gloria
Bachmann, Kai
Goebels, Hanna
Heß, Leonard
Koch, Martina
Langeneckert, Annika
Lunemann, Sebastian
Oldhafer, Karl J.
Pfeifer, Caroline
Poch, Tobias
Richert, Laura
Schramm, Christoph
Wahib, Ramez
Bunders, Madeleine J.
Altfeld, Marcus
author_sort Salzberger, Wilhelm
collection PubMed
description Metabolism is a critical basis for immune cell functionality. It was recently shown that NK cell subsets from peripheral blood modulate their expression of nutrient receptors following cytokine stimulation, demonstrating that NK cells can adjust to changes in metabolic requirements. As nutrient availability in blood and tissues can significantly differ, we examined NK cells isolated from paired blood-liver and blood-spleen samples and compared expression of the nutrient transporters Glut1, CD98 and CD71. CD56(bright) tissue-resident (CXCR6(+)) NK cells derived from livers and spleens expressed lower levels of Glut1 but higher levels of the amino acid transporter CD98 following stimulation than CD56(bright) NK cells from peripheral blood. In line with that, CD56(dim) NK cells, which constitute the main NK cell population in the peripheral blood, expressed higher levels of Glut1 and lower levels of CD98 and CD71 compared to liver CD56(bright) NK cells. Our results show that NK cells from peripheral blood differ from liver- and spleen-resident NK cells in the expression profile of nutrient transporters, consistent with a cell-adaptation to the different nutritional environment in these compartments.
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spelling pubmed-60543882018-07-27 Tissue-resident NK cells differ in their expression profile of the nutrient transporters Glut1, CD98 and CD71 Salzberger, Wilhelm Martrus, Gloria Bachmann, Kai Goebels, Hanna Heß, Leonard Koch, Martina Langeneckert, Annika Lunemann, Sebastian Oldhafer, Karl J. Pfeifer, Caroline Poch, Tobias Richert, Laura Schramm, Christoph Wahib, Ramez Bunders, Madeleine J. Altfeld, Marcus PLoS One Research Article Metabolism is a critical basis for immune cell functionality. It was recently shown that NK cell subsets from peripheral blood modulate their expression of nutrient receptors following cytokine stimulation, demonstrating that NK cells can adjust to changes in metabolic requirements. As nutrient availability in blood and tissues can significantly differ, we examined NK cells isolated from paired blood-liver and blood-spleen samples and compared expression of the nutrient transporters Glut1, CD98 and CD71. CD56(bright) tissue-resident (CXCR6(+)) NK cells derived from livers and spleens expressed lower levels of Glut1 but higher levels of the amino acid transporter CD98 following stimulation than CD56(bright) NK cells from peripheral blood. In line with that, CD56(dim) NK cells, which constitute the main NK cell population in the peripheral blood, expressed higher levels of Glut1 and lower levels of CD98 and CD71 compared to liver CD56(bright) NK cells. Our results show that NK cells from peripheral blood differ from liver- and spleen-resident NK cells in the expression profile of nutrient transporters, consistent with a cell-adaptation to the different nutritional environment in these compartments. Public Library of Science 2018-07-20 /pmc/articles/PMC6054388/ /pubmed/30028872 http://dx.doi.org/10.1371/journal.pone.0201170 Text en © 2018 Salzberger et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Salzberger, Wilhelm
Martrus, Gloria
Bachmann, Kai
Goebels, Hanna
Heß, Leonard
Koch, Martina
Langeneckert, Annika
Lunemann, Sebastian
Oldhafer, Karl J.
Pfeifer, Caroline
Poch, Tobias
Richert, Laura
Schramm, Christoph
Wahib, Ramez
Bunders, Madeleine J.
Altfeld, Marcus
Tissue-resident NK cells differ in their expression profile of the nutrient transporters Glut1, CD98 and CD71
title Tissue-resident NK cells differ in their expression profile of the nutrient transporters Glut1, CD98 and CD71
title_full Tissue-resident NK cells differ in their expression profile of the nutrient transporters Glut1, CD98 and CD71
title_fullStr Tissue-resident NK cells differ in their expression profile of the nutrient transporters Glut1, CD98 and CD71
title_full_unstemmed Tissue-resident NK cells differ in their expression profile of the nutrient transporters Glut1, CD98 and CD71
title_short Tissue-resident NK cells differ in their expression profile of the nutrient transporters Glut1, CD98 and CD71
title_sort tissue-resident nk cells differ in their expression profile of the nutrient transporters glut1, cd98 and cd71
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054388/
https://www.ncbi.nlm.nih.gov/pubmed/30028872
http://dx.doi.org/10.1371/journal.pone.0201170
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