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Tytuł pozycji:

Contrasting functional responses of resident Kupffer cells and recruited liver macrophages to irradiation and liver X receptor stimulation.

Tytuł:
Contrasting functional responses of resident Kupffer cells and recruited liver macrophages to irradiation and liver X receptor stimulation.
Autorzy:
Ishikiriyama T; Department of Immunology and Microbiology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Nakashima H; Department of Immunology and Microbiology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Endo-Umeda K; Division of Biochemistry, Department of Biomedical Sciences, Nihon University School of Medicine, Itabashi, Tokyo, Japan.
Nakashima M; Department of Immunology and Microbiology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Ito S; Department of Nephrology and Endocrinology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Kinoshita M; Department of Immunology and Microbiology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Ikarashi M; Department of Immunology and Microbiology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Makishima M; Division of Biochemistry, Department of Biomedical Sciences, Nihon University School of Medicine, Itabashi, Tokyo, Japan.
Seki S; Department of Immunology and Microbiology, National Defense Medical College, Tokorozawa, Saitama, Japan.
Źródło:
PloS one [PLoS One] 2021 Jul 23; Vol. 16 (7), pp. e0254886. Date of Electronic Publication: 2021 Jul 23 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Original Publication: San Francisco, CA : Public Library of Science
MeSH Terms:
Phagocytosis*
Kupffer Cells/*immunology
Liver/*immunology
Liver X Receptors/*metabolism
Animals ; Cells, Cultured ; Lipid Metabolism ; Lipoproteins, LDL/metabolism ; Liver/cytology ; Liver/radiation effects ; Liver X Receptors/genetics ; Mice ; Mice, Inbred C57BL ; Tumor Necrosis Factor-alpha/metabolism
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Substance Nomenclature:
0 (Lipoproteins, LDL)
0 (Liver X Receptors)
0 (Tumor Necrosis Factor-alpha)
Entry Date(s):
Date Created: 20210723 Date Completed: 20211104 Latest Revision: 20211104
Update Code:
20240105
PubMed Central ID:
PMC8301620
DOI:
10.1371/journal.pone.0254886
PMID:
34297734
Czasopismo naukowe
In the murine liver, there are two major macrophage populations, namely resident Kupffer cells (resKCs) with phagocytic activity and recruited macrophages (recMφs) with cytokine-producing capacity. This study was performed to clarify the functional differences between these two populations, focusing on their susceptibility to radiation and response to stimulation via liver X receptors (LXRs), which are implicated in cholesterol metabolism and immune regulation. Liver mononuclear cells (MNCs) were obtained from C57BL/6 (WT) mice with or without 2 Gy irradiation, and the phagocytic activity against Escherichia coli (E. coli) as well as TNF-α production were compared between the two macrophage populations. To assess LXR functions, phagocytosis, TNF-α production, and endocytosis of acetylated low-density lipoprotein (LDL) were compared after synthetic LXR ligand stimulation. Furthermore, LXRα/β knockout (KO) mice and LXRα KO mice were compared with WT mice. Irradiation decreased intracellular TNF-α production by recMφs but did not affect the phagocytic activity of resKCs. In vitro LXR stimulation enhanced E. coli phagocytosis by resKCs but decreased E. coli-stimulated TNF-α production by recMφs. Phagocytic activity and acetylated LDL endocytosis were decreased in both LXRα/β KO mice and LXRα KO mice, with serum TNF-α levels after E. coli injection in the former being higher than those in WT mice. In conclusion, resKCs and recMφs exhibited different functional features in response to radiation and LXR stimulation, highlighting their distinct roles liver immunity and lipid metabolism.
Competing Interests: The authors have declared that no competing interests exist.
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