Thapsigargin blocks Pseudomonas aeruginosa homoserine lactone-induced apoptosis in airway epithelia

Am J Physiol Cell Physiol. 2014 May 1;306(9):C844-55. doi: 10.1152/ajpcell.00002.2014. Epub 2014 Mar 5.

Abstract

Pseudomonas aeruginosa secretes N-(3-oxododecanoyl)-homoserine lactone (C12) as a quorum-sensing molecule to regulate gene expression. Micromolar concentrations are found in the airway surface liquid of infected lungs. Exposure of the airway surface to C12 caused a loss of transepithelial resistance within 1 h that was accompanied by disassembly of tight junctions, as indicated by relocation of the tight junction protein zonula occludens 1 from the apical to the basolateral pole and into the cytosol of polarized human airway epithelial cell cultures (Calu-3 and primary tracheal epithelial cells). These effects were blocked by carbobenzoxy-valyl-alanyl-aspartyl-[O-methyl]-fluoromethylketone, a pan-caspase blocker, indicating that tight junction disassembly was an early event in C12-triggered apoptosis. Short-duration (10 min) pretreatment of airway epithelial (Calu-3 and JME) cells with 1 μM thapsigargin (Tg), an inhibitor of Ca(2+) uptake into the endoplasmic reticulum (ER), was found to be protective against the C12-induced airway epithelial barrier breakdown and also against other apoptosis-related effects, including shrinkage and fragmentation of nuclei, activation of caspase 3/7 (the executioner caspase in apoptosis), release of ER-targeted redox-sensitive green fluorescent protein into the cytosol, and depolarization of mitochondrial membrane potential. Pretreatment of Calu-3 airway cell monolayers with BAPTA-AM [to buffer cytosolic Ca(2+) concentration (Cacyto)] or Ca(2+)-free solution + BAPTA-AM reduced C12 activation of apoptotic events, suggesting that C12-triggered apoptosis may involve Ca(2+). Because C12 and Tg reduced Ca(2+) concentration in the ER and increased Cacyto, while Tg increased mitochondrial Ca(2+) concentration (Camito) and C12 reduced Camito, it is proposed that Tg may reduce C12-induced apoptosis in host cells not by raising Cacyto, but by preventing C12-induced decreases in Camito.

Keywords: calcium; caspase; endoplasmic reticulum; innate immunity; mitochondria; tight junctions; zonula occludens 1.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Butyrolactone / analogs & derivatives*
  • 4-Butyrolactone / metabolism
  • Apoptosis / drug effects*
  • Calcium / metabolism*
  • Caspase 3 / metabolism
  • Caspase 7 / metabolism
  • Cell Line
  • Chelating Agents / pharmacology
  • Cytoprotection
  • Electric Impedance
  • Endoplasmic Reticulum / drug effects
  • Endoplasmic Reticulum / metabolism
  • Endoplasmic Reticulum / pathology
  • Enzyme Activation
  • Humans
  • Lung / drug effects*
  • Lung / metabolism
  • Lung / microbiology
  • Lung / pathology
  • Membrane Potential, Mitochondrial / drug effects
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondria / pathology
  • Primary Cell Culture
  • Protein Transport
  • Pseudomonas aeruginosa / metabolism*
  • Thapsigargin / pharmacology*
  • Tight Junctions / drug effects
  • Tight Junctions / metabolism
  • Tight Junctions / pathology
  • Time Factors
  • Trachea / drug effects*
  • Trachea / metabolism
  • Trachea / microbiology
  • Trachea / pathology
  • Zonula Occludens-1 Protein / metabolism

Substances

  • Chelating Agents
  • TJP1 protein, human
  • Zonula Occludens-1 Protein
  • homoserine lactone
  • Thapsigargin
  • CASP3 protein, human
  • CASP7 protein, human
  • Caspase 3
  • Caspase 7
  • 4-Butyrolactone
  • Calcium