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

PLoS One. 2021 Jul 23;16(7):e0254886. doi: 10.1371/journal.pone.0254886. eCollection 2021.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Kupffer Cells / immunology*
  • Lipid Metabolism
  • Lipoproteins, LDL / metabolism
  • Liver / cytology
  • Liver / immunology*
  • Liver / radiation effects
  • Liver X Receptors / genetics
  • Liver X Receptors / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Phagocytosis*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Lipoproteins, LDL
  • Liver X Receptors
  • Tumor Necrosis Factor-alpha

Grants and funding

JSPS KAKENHI Grant Number JP 16K08751 (H N) JSPS KAKENHI Grant Number JP 20K07438 (H N) JSPS KAKENHI Grant Number JP 25860248 (K.E.-U) JSPS KAKENHI Grant Number JP 16K19061 (K.E.-U) Nihon University School of Medicine Toki Fund Research Grant (K.E.-U) JSPS KAKENHI Grant Number JP 17K08611 (M N) JSPS KAKENHI Grant Number JP 18K02907 (M K).