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Liver X receptors regulate natural killer T cell population and antitumor activity in the liver of mice

The nuclear receptors liver X receptor α (LXRα) and LXRβ are lipid sensors that regulate lipid metabolism and immunity. Natural killer T (NKT) cells, a T cell subset expressing surface markers of both natural killer cells and T lymphocytes and involved in antitumor immunity, are another abundant imm...

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Autores principales: Endo-Umeda, Kaori, Nakashima, Hiroyuki, Uno, Shigeyuki, Toyoshima, Shota, Umeda, Naoki, Komine-Aizawa, Shihoko, Seki, Shuhji, Makishima, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604965/
https://www.ncbi.nlm.nih.gov/pubmed/34799646
http://dx.doi.org/10.1038/s41598-021-02062-z
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author Endo-Umeda, Kaori
Nakashima, Hiroyuki
Uno, Shigeyuki
Toyoshima, Shota
Umeda, Naoki
Komine-Aizawa, Shihoko
Seki, Shuhji
Makishima, Makoto
author_facet Endo-Umeda, Kaori
Nakashima, Hiroyuki
Uno, Shigeyuki
Toyoshima, Shota
Umeda, Naoki
Komine-Aizawa, Shihoko
Seki, Shuhji
Makishima, Makoto
author_sort Endo-Umeda, Kaori
collection PubMed
description The nuclear receptors liver X receptor α (LXRα) and LXRβ are lipid sensors that regulate lipid metabolism and immunity. Natural killer T (NKT) cells, a T cell subset expressing surface markers of both natural killer cells and T lymphocytes and involved in antitumor immunity, are another abundant immune cell type in the liver. The potential function of the metabolic regulators LXRα/β in hepatic NKT cells remains unknown. In this study, we examined the role of LXRα and LXRβ in NKT cells using mice deficient for LXRα and/or LXRβ, and found that hepatic invariant NKT (iNKT) cells are drastically decreased in LXRα/β-KO mice. Cytokine production stimulated by the iNKT cell activator α-galactosylceramide was impaired in LXRα/β-KO hepatic mononuclear cells and in LXRα/β-KO mice. iNKT cell-mediated antitumor effect was also disturbed in LXRα/β-KO mice. LXRα/β-KO mice transplanted with wild-type bone marrow showed decreased iNKT cells in the liver and spleen. The thymus of LXRα/β-KO mice showed a decreased population of iNKT cells. In conclusion, LXRα and LXRβ are essential for NKT cell-mediated immunity, such as cytokine production and hepatic antitumor activity, and are involved in NKT cell development in immune tissues, such as the thymus.
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spelling pubmed-86049652021-11-22 Liver X receptors regulate natural killer T cell population and antitumor activity in the liver of mice Endo-Umeda, Kaori Nakashima, Hiroyuki Uno, Shigeyuki Toyoshima, Shota Umeda, Naoki Komine-Aizawa, Shihoko Seki, Shuhji Makishima, Makoto Sci Rep Article The nuclear receptors liver X receptor α (LXRα) and LXRβ are lipid sensors that regulate lipid metabolism and immunity. Natural killer T (NKT) cells, a T cell subset expressing surface markers of both natural killer cells and T lymphocytes and involved in antitumor immunity, are another abundant immune cell type in the liver. The potential function of the metabolic regulators LXRα/β in hepatic NKT cells remains unknown. In this study, we examined the role of LXRα and LXRβ in NKT cells using mice deficient for LXRα and/or LXRβ, and found that hepatic invariant NKT (iNKT) cells are drastically decreased in LXRα/β-KO mice. Cytokine production stimulated by the iNKT cell activator α-galactosylceramide was impaired in LXRα/β-KO hepatic mononuclear cells and in LXRα/β-KO mice. iNKT cell-mediated antitumor effect was also disturbed in LXRα/β-KO mice. LXRα/β-KO mice transplanted with wild-type bone marrow showed decreased iNKT cells in the liver and spleen. The thymus of LXRα/β-KO mice showed a decreased population of iNKT cells. In conclusion, LXRα and LXRβ are essential for NKT cell-mediated immunity, such as cytokine production and hepatic antitumor activity, and are involved in NKT cell development in immune tissues, such as the thymus. Nature Publishing Group UK 2021-11-19 /pmc/articles/PMC8604965/ /pubmed/34799646 http://dx.doi.org/10.1038/s41598-021-02062-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Endo-Umeda, Kaori
Nakashima, Hiroyuki
Uno, Shigeyuki
Toyoshima, Shota
Umeda, Naoki
Komine-Aizawa, Shihoko
Seki, Shuhji
Makishima, Makoto
Liver X receptors regulate natural killer T cell population and antitumor activity in the liver of mice
title Liver X receptors regulate natural killer T cell population and antitumor activity in the liver of mice
title_full Liver X receptors regulate natural killer T cell population and antitumor activity in the liver of mice
title_fullStr Liver X receptors regulate natural killer T cell population and antitumor activity in the liver of mice
title_full_unstemmed Liver X receptors regulate natural killer T cell population and antitumor activity in the liver of mice
title_short Liver X receptors regulate natural killer T cell population and antitumor activity in the liver of mice
title_sort liver x receptors regulate natural killer t cell population and antitumor activity in the liver of mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604965/
https://www.ncbi.nlm.nih.gov/pubmed/34799646
http://dx.doi.org/10.1038/s41598-021-02062-z
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