Transduced PEP-1-AMPK inhibits the LPS-induced expression of COX-2 and iNOS in Raw264.7 cells

BMB Rep. 2010 Jan;43(1):40-5. doi: 10.5483/bmbrep.2010.43.1.040.

Abstract

AMP-activated protein kinase (AMPK) is a heterotrimeric enzyme that plays a central role in cellular metabolic stress. Modulation of nitric oxide (NO) and cyclooxygenase-2 (COX-2) is considered a promising approach for the treatment of inflammation and neuronal diseases. In this study, the AMPK gene was fused in-frame with PEP-1 peptide in a bacterial expression vector to produce a PEP-1-AMPK fusion protein. Expressed and purified PEP-1-AMPK fusion proteins were transduced efficiently into macrophage Raw 264.7 cells in a time- and dose-dependent manner. Furthermore, transduced PEP-1-AMPK fusion protein markedly inhibited LPS-induced iNOS and COX-2 expression. These results suggest that the PEP-1-AMPK fusion protein can be used for the protein therapy of COX-2 and NO-related disorders such as inflammation and neuronal diseases. [BMB reports 2010; 43(1): 40-45].

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / genetics*
  • AMP-Activated Protein Kinases / metabolism
  • Animals
  • Cell Line, Tumor
  • Cyclooxygenase 2 / metabolism*
  • Cysteamine / analogs & derivatives*
  • Cysteamine / metabolism
  • Lipopolysaccharides / pharmacology*
  • Mice
  • Nitric Oxide Synthase Type II / metabolism*
  • Peptides / genetics*
  • Peptides / metabolism
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / isolation & purification
  • Time Factors
  • Transduction, Genetic

Substances

  • Lipopolysaccharides
  • Pep-1 peptide
  • Peptides
  • Recombinant Fusion Proteins
  • Cysteamine
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
  • Cyclooxygenase 2
  • AMP-Activated Protein Kinases