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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Veröffentlicht in:Scientific reports 2021-11, Vol.11 (1), p.22595-22595, Article 22595
Hauptverfasser: Endo-Umeda, Kaori, Nakashima, Hiroyuki, Uno, Shigeyuki, Toyoshima, Shota, Umeda, Naoki, Komine-Aizawa, Shihoko, Seki, Shuhji, Makishima, Makoto
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container_title Scientific reports
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creator Endo-Umeda, Kaori
Nakashima, Hiroyuki
Uno, Shigeyuki
Toyoshima, Shota
Umeda, Naoki
Komine-Aizawa, Shihoko
Seki, Shuhji
Makishima, Makoto
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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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. 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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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>34799646</pmid><doi>10.1038/s41598-021-02062-z</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record>
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subjects 631/250/580
631/337
Animals
Antineoplastic Agents - pharmacology
Antitumor activity
Bone marrow
Bone Marrow - metabolism
Bone Marrow Transplantation
Cell-mediated immunity
Cytokines
Cytokines - metabolism
Galactosylceramide
Galactosylceramides - metabolism
Hepatocytes
Humanities and Social Sciences
Killer Cells, Natural - metabolism
Leukocytes (mononuclear)
Leukocytes, Mononuclear - metabolism
Lipid metabolism
Liver
Liver - drug effects
Liver - metabolism
Liver Neoplasms - pathology
Liver X receptors
Liver X Receptors - metabolism
Lymphocytes
Lymphocytes T
Male
Mice
Mice, Inbred C57BL
Mice, Knockout
multidisciplinary
Multidisciplinary Sciences
Natural killer cells
Neoplasm Metastasis
Nuclear receptors
Rodents
Science
Science & Technology
Science & Technology - Other Topics
Science (multidisciplinary)
Spleen
Spleen - cytology
Spleen - metabolism
Surface markers
Thymocytes - cytology
Thymus
Thymus gland
title Liver X receptors regulate natural killer T cell population and antitumor activity in the liver of mice
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