Molecular basis of early epithelial response to streptococcal exotoxin: role of STIM1 and Orai1 proteins

Cell Microbiol. 2012 Mar;14(3):299-315. doi: 10.1111/j.1462-5822.2011.01724.x. Epub 2011 Dec 13.

Abstract

Streptolysin O (SLO) is a cholesterol-dependent cytolysin (CDC) from Streptococcus pyogenes. SLO induces diverse types of Ca(2+) signalling in host cells which play a key role in membrane repair and cell fate determination. The mechanisms behind SLO-induced Ca(2+) signalling remain poorly understood. Here, we show that in NCI-H441 cells, wild-type SLO as well as non-pore-forming mutant induces long-lasting intracellular Ca(2+) oscillations via IP(3) -mediated depletion of intracellular stores and activation of store-operated Ca(2+) (SOC) entry. SLO-induced activation of SOC entry was confirmed by Ca(2+) add-back experiments, pharmacologically and by overexpression as well as silencing of STIM1 and Orai1 expression. SLO also activated SOC entry in primary cultivated alveolar type II (ATII) cells but Ca(2+) oscillations were comparatively short-lived in nature. Comparison of STIM1 and Orai1 revealed a differential expression pattern in H441 and ATII cells. Overexpression of STIM1 and Orai1 proteins in ATII cells changed the short-lived oscillatory response into a long-lived one. Thus, we conclude that SLO-mediated Ca(2+) signalling involves Ca(2+) release from intracellular stores and STIM1/Orai1-dependent SOC entry. The phenotype of Ca(2+) signalling depends on STIM1 and Orai1 expression levels. Our findings suggest a new role for SOC entry-associated proteins in S. pyogenes-induced lung infection and pneumonia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / pharmacology
  • Bacterial Proteins / physiology
  • Calcium / metabolism
  • Calcium Channels / genetics
  • Calcium Channels / metabolism
  • Calcium Channels / physiology*
  • Calcium Signaling*
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Diglycerides / metabolism
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism*
  • Host-Pathogen Interactions
  • Humans
  • Inositol 1,4,5-Trisphosphate / metabolism
  • Lung / pathology
  • Male
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Membrane Proteins / physiology*
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism
  • Neoplasm Proteins / physiology*
  • ORAI1 Protein
  • Primary Cell Culture
  • Protein Transport
  • Rats
  • Rats, Sprague-Dawley
  • Respiratory Tract Infections / microbiology
  • Streptococcal Infections / microbiology
  • Streptococcus pyogenes / physiology
  • Streptolysins / pharmacology
  • Streptolysins / physiology*
  • Stromal Interaction Molecule 1

Substances

  • Bacterial Proteins
  • Calcium Channels
  • Diglycerides
  • Membrane Proteins
  • Neoplasm Proteins
  • ORAI1 Protein
  • ORAI1 protein, human
  • STIM1 protein, human
  • Streptolysins
  • Stromal Interaction Molecule 1
  • streptolysin O
  • Inositol 1,4,5-Trisphosphate
  • Calcium