High-mobility group box 1 enhances the inflammatory process in diabetic lung

Arch Biochem Biophys. 2015 Oct 1:583:55-64. doi: 10.1016/j.abb.2015.07.020. Epub 2015 Aug 6.

Abstract

Diabetes mellitus generates metabolic changes associated with inflammatory events that may eventually affect all body tissues. Both high-mobility group box 1 (HMGB1) and β-catenin are active players in inflammation. The study aimed to determine whether HMGB1 modulates the β-catenin activity in supporting inflammation, using an experimental type 1 diabetes mouse model. The protein and gene expression of HMGB1 were significantly increased (2-fold) in the diabetic lung compared to control and were positively correlated with the HMGB1 levels detected in serum. Co-immunoprecipitation of HMGB1 with RAGE co-exists with activation of PI3K/AKT1 and NF-kB signaling pathways. At the same time β-catenin was increased in nuclear fraction (3.5 fold) while it was down-regulated in diabetic plasma membrane (2-fold). There was no difference of β-catenin gene expression between the control and diabetic mice. β-Catenin phosphorylation at Ser552 was higher in diabetic nuclear fraction, suggesting that AKT1 activation promotes β-catenin nuclear translocation. In addition, c-Jun directly binds β-catenin indicating the transcriptional activity of β-catenin in diabetes, sustained by significantly COX2 increase by 6-fold in the cytosolic extract of diabetic lung compared to control. Taken together, the data support the new concept that HMGB1 maintains the inflammation through RAGE/AKT1/β-catenin pathway in the diabetic lung.

Keywords: AKT1; Diabetes mellitus; HMGB1; Lung; RAGE; β-Catenin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Nucleus / metabolism
  • Diabetes Mellitus, Experimental / complications*
  • HMGB1 Protein / physiology*
  • Mass Spectrometry
  • Mice
  • Mice, Transgenic
  • Phosphorylation
  • Pneumonia / complications
  • Pneumonia / metabolism
  • Pneumonia / physiopathology*
  • Proteome
  • Proto-Oncogene Proteins c-akt / metabolism
  • Receptor for Advanced Glycation End Products / metabolism
  • beta Catenin / metabolism

Substances

  • Ager protein, mouse
  • HMGB1 Protein
  • HMGB1 protein, mouse
  • Proteome
  • Receptor for Advanced Glycation End Products
  • beta Catenin
  • Akt1 protein, mouse
  • Proto-Oncogene Proteins c-akt