Relationship of Cx43 regulation of vascular permeability to osteopontin-tight junction protein pathway after sepsis in rats

Am J Physiol Regul Integr Comp Physiol. 2018 Jan 1;314(1):R1-R11. doi: 10.1152/ajpregu.00443.2016. Epub 2017 Oct 4.

Abstract

Our previous study demonstrated that connexin (Cx)43 participated in the regulation of vascular permeability in severe sepsis. Osteopontin (OPN) has been demonstrated to participate in the occurrence of atherosclerosis, inflammation, as well as the adhesion and migration of cells. It is not clear whether OPN is involved in Cx43 regulating vascular permeability after sepsis and if it is related to tight-junction proteins. with the use of cecal ligation and puncture (CLP)-induced septic rats and lipopolysaccharide (LPS)-treated pulmonary vein vascular endothelial cells (VECs), the role of zona occuldens 1 (ZO-1) and claudin-5 in Cx43 regulation of vascular permeability and its relationship to OPN were investigated in the present study. The results showed that the expression of ZO-1 and claudin-5 in pulmonary vein were decreased in CLP rats and LPS-treated pulmonary vein VECs. Cx43-overexpressed lentivirus induced the degradation of ZO-1 and claudin-5, while Cx43 RNAi lentivirus abrogated the degradation of ZO-1 and claudin-5 induced by LPS. The vascular permeability and expression of OPN in pulmonary veins were significantly increased in CLP rats and LPS-treated pulmonary vein VECs. Silencing OPN by OPN RNAi lentivirus inhibited the vascular hyperpermeability induced by LPS. Overexpressed Cx43 lentivirus increased the expression of OPN and vascular permeability and downregulated the expression of ZO-1 and claudin-5 in pulmonary vein VECs. Silencing OPN by OPN RNAi lentivirus inhibited the effects of Cx43-overexpressed lentivirus on downregulation of ZO-1 and claudin-5 and vascular hyperpermeability in pulmonary vein VECs. Transfection of specific double-stranded RNA targeting to β-catenin and T-cell factor-4 (Tcf-4) abolished the upregulation of OPN induced by Cx43 overexpression. These results suggest that OPN participates in the regulation of vascular permeability by Cx43 after sepsis. Cx43 upregulation of OPN is via the Tcf-4/β-catenin transcription pathway; OPN increases vascular permeability by downregulating the expression of the tight junction proteins ZO-1 and claudin-5.

Keywords: OPN; connexin; sepsis; vascular permeability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Capillary Permeability*
  • Cells, Cultured
  • Claudin-5 / genetics
  • Claudin-5 / metabolism
  • Connexin 43 / genetics
  • Connexin 43 / metabolism*
  • Disease Models, Animal
  • Endothelial Cells / metabolism*
  • Endothelial Cells / microbiology
  • Female
  • Lung / blood supply*
  • Male
  • Osteopontin / genetics
  • Osteopontin / metabolism*
  • Pulmonary Veins / metabolism*
  • Pulmonary Veins / microbiology
  • Pulmonary Veins / physiopathology
  • Rats, Sprague-Dawley
  • Sepsis / metabolism*
  • Sepsis / microbiology
  • Sepsis / physiopathology
  • Signal Transduction
  • Tight Junctions / metabolism*
  • Tight Junctions / microbiology
  • Time Factors
  • Transcription Factor 4 / genetics
  • Transcription Factor 4 / metabolism
  • Zonula Occludens-1 Protein / genetics
  • Zonula Occludens-1 Protein / metabolism
  • beta Catenin / genetics
  • beta Catenin / metabolism

Substances

  • Claudin-5
  • Cldn5 protein, rat
  • Connexin 43
  • Ctnnb1 protein, rat
  • Gja1 protein, rat
  • Spp1 protein, rat
  • Tcf4 protein, rat
  • Tjp1 protein, rat
  • Transcription Factor 4
  • Zonula Occludens-1 Protein
  • beta Catenin
  • Osteopontin