Alteration of lysosome fusion and low-grade inflammation mediated by super-low-dose endotoxin

J Biol Chem. 2015 Mar 6;290(10):6670-8. doi: 10.1074/jbc.M114.611442. Epub 2015 Jan 13.

Abstract

Subclinical super-low-dose endotoxin LPS is a risk factor for the establishment of low-grade inflammation during the pathogenesis and progression of chronic diseases. However, the underlying mechanisms are not well understood. At the cellular level, a disruption of lysosome fusion with endosomes or autophagosomes may contribute to the potentiation of low-grade inflammation. In this study, we identified that subclinical super-low-dose endotoxin LPS can potently inhibit the process of endosome acidification and lysosome fusion with endosomes or autophagosomes in primary macrophages. Super-low-dose LPS induced the inhibitory phosphorylation of VPS34, thus leading to the disruption of endosome-lysosome fusion. This effect may depend upon the clearance and relocation of Tollip in macrophages by super-low-dose LPS. Consistent with this notion, Tollip-deficient macrophages had constitutively elevated levels of VPS34 inhibitory phosphorylation and constitutive disruption of endosome-lysosome fusion. By employing a skin excision wound-healing model, we observed that Tollip-deficient mice had significantly elevated levels of cell stress and reduced wound repair. This study reveals a novel mechanism responsible for the modulation of endosome-lysosome fusion and low-grade inflammation in innate macrophages.

Keywords: Cell Signaling; Endosome-Lysosome Fusion; Innate Immunity; Lipopolysaccharide (LPS); Low-grade Inflammation; Lysosome; Macrophage; Macrophages; Super-low-dose Endotoxin.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Autophagy / immunology*
  • Endosomes / drug effects
  • Endosomes / immunology
  • Humans
  • Immunity, Innate*
  • Inflammation / chemically induced
  • Inflammation / immunology*
  • Inflammation / pathology
  • Intracellular Signaling Peptides and Proteins / genetics
  • Lipopolysaccharides / toxicity*
  • Lysosomes / drug effects
  • Lysosomes / immunology*
  • Lysosomes / pathology
  • Macrophages / drug effects
  • Macrophages / immunology
  • Mice
  • Mice, Knockout

Substances

  • Intracellular Signaling Peptides and Proteins
  • Lipopolysaccharides
  • TOLLIP protein, human