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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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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. |
format | Online Article Text |
id | pubmed-6054388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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