Mannose prevents acute lung injury through mannose receptor pathway and contributes to regulate PPARγ and TGF-β1 level

Int J Clin Exp Pathol. 2015 Jun 1;8(6):6214-24. eCollection 2015.

Abstract

Mannose has been reported to prevent acute lung injury (ALI), and mannose receptor (MR) has been demonstrated to have a role. The rationale for this study is to characterize the mechanism by which mannose and MR prevent lipopolysaccharide (LPS)-induced ALI. Male ICR mice were pretreated mannose by intravenous injection 5 min before and 3 h after intratracheal instillation of LPS. Pathological changes, proinflammatory mediator, peroxisome proliferator activated receptor gamma (PPARγ), MR, and transforming growth factor β1 (TGF-β1) levels were determined. The RAW264.7 cells were pretreated with mannose and stimulated with LPS for 3 h. Proinflammatory mediator and TGF-β1 in the culture media, PPARγ, MR, and TGF-β1 expression in RAW 264.7 cells were measured. Mannose markedly attenuated the LPS-induced histological alterations and inhibited the production of proinflammatory mediator in mice and in RAW 264.7 cells. Mannose increased PPARγ and MR expression, and inhibited TGF-β1 stimulated by LPS. Interestingly, competitive inhibition of MR with mannan was associated with elimination of the anti-inflammatory effects of mannose, and reversed effects of mannose of regulation to PPARγ and TGF-β1. MR is important in increasing PPARγ and decreasing TGF-β1 expression and plays a critical role in mannose's protection against ALI.

Keywords: Acute lung injury; PPARγ; TGF-β1; anti-inflammation; mannose; mannose receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Lung Injury / metabolism*
  • Acute Lung Injury / prevention & control
  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Blotting, Western
  • Cells, Cultured
  • Disease Models, Animal
  • Enzyme-Linked Immunosorbent Assay
  • Lectins, C-Type / metabolism*
  • Male
  • Mannose / pharmacology*
  • Mannose Receptor
  • Mannose-Binding Lectins / metabolism*
  • Mice
  • Mice, Inbred ICR
  • PPAR gamma / metabolism*
  • Real-Time Polymerase Chain Reaction
  • Receptors, Cell Surface / metabolism*
  • Signal Transduction / drug effects
  • Transforming Growth Factor beta1 / metabolism*

Substances

  • Anti-Inflammatory Agents
  • Lectins, C-Type
  • Mannose Receptor
  • Mannose-Binding Lectins
  • PPAR gamma
  • Receptors, Cell Surface
  • Transforming Growth Factor beta1
  • Mannose