Inhibition of insulin-like growth factor receptor-1 reduces necroptosis-related markers and attenuates LPS-induced lung injury in mice

Biochem Biophys Res Commun. 2018 Apr 15;498(4):877-883. doi: 10.1016/j.bbrc.2018.03.074. Epub 2018 Mar 14.

Abstract

Insulin-like growth factor-1 (IGF-1) levels are known to increase in the bronchoalveolar lavage fluid (BALF) of patients with acute respiratory distress syndrome. Herein, we investigated the role of IGF-1 in lipopolysaccharide (LPS)-induced lung injury. In LPS-treated cells, expressions of receptor-interacting protein 3 (RIP3) and phosphorylated mixed lineage kinase domain-like protein (MLKL) were decreased in IGF-1 receptor small interfering RNA (siRNA)-treated cells compared to control cells. The levels of pro-inflammatory cytokines including interleukin (IL)-1β, IL-6, IL-10, tumour necrosis factor-α, and macrophage inflammatory protein 2/C-X-C motif chemokine ligand 2 in the supernatant were significantly reduced in IGF-1 receptor siRNA-treated cells compared to control cells. In LPS-induced murine lung injury model, total cell counts, polymorphonuclear leukocytes counts, and pro-inflammatory cytokine levels in the BALF were significantly lower and histologically detected lung injury was less common in the group treated with IGF-1 receptor monoclonal antibody compared to the non-treated group. On western blotting, RIP3 and phosphorylated MLKL expressions were relatively decreased in the IGF-1 receptor monoclonal antibody group compared to the non-treated group. IGF-1 may be associated with RIP3-mediated necroptosis in vitro, while blocking of the IGF-1 pathway may reduce LPS-induced lung injuries in vivo.

Keywords: Adult; IGF-1 receptor; Lipopolysaccharide; Lung injury; Necroptosis; Respiratory distress syndrome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Apoptosis / drug effects
  • Bronchoalveolar Lavage Fluid / chemistry
  • Bronchoalveolar Lavage Fluid / cytology
  • Bronchoalveolar Lavage Fluid / immunology
  • Cadherins / metabolism
  • Lipopolysaccharides
  • Lung / metabolism
  • Lung Injury / chemically induced
  • Lung Injury / prevention & control*
  • Macrophages / metabolism
  • Mice
  • Necrosis / etiology*
  • Receptor, IGF Type 1 / antagonists & inhibitors
  • Receptor, IGF Type 1 / pharmacology*
  • Receptor, IGF Type 1 / physiology
  • Receptor-Interacting Protein Serine-Threonine Kinases / metabolism

Substances

  • Antigens, CD
  • Cadherins
  • Lipopolysaccharides
  • cadherin 5
  • Receptor, IGF Type 1
  • Receptor-Interacting Protein Serine-Threonine Kinases
  • Ripk3 protein, mouse