SUMOylation attenuates sensitivity toward hypoxia- or desferroxamine-induced injury by modulating adaptive responses in salivary epithelial cells

Am J Pathol. 2006 May;168(5):1452-63. doi: 10.2353/ajpath.2006.050782.

Abstract

Hypoxic stress activates various signal transduction pathways including posttranslational modification with the ubiquitin-like SUMO protein (SUMOylation). However, the molecular mechanisms by which SUMOylation regulates hypoxic responses remain unclear. Here, we investigated the ability of rat salivary Pa-4 epithelial cells to resist cell injury elicited by 1% O(2)- or hypoxia-mimetic desferroxamine (DFO)-stimulated SUMOylation processes. By using Pa-4 cells stably transduced with lenti-SUMO-1 and a cell-permeant peptide harboring SUMO-binding motif to interfere with SUMO-dependent protein-protein interactions, we demonstrate that SUMOylation augments cell survival against DFO treatment. This appeared to be partly mediated through attenuation of Protein Kinase C (PKC)-delta activation and caspase-3 cleavage, hallmarks of pro-apoptotic signaling. Intriguingly, DFO-induced phosphorylation of DNA damage marker ataxia-telangiectasia-mutated protein S1981 preceded activation of PKCdelta and caspase-3. Constitutive SUMOylation facilitated 1% O(2)- or DFO-induced nuclear factor kappaB transactivation, possibly via activation of genotoxic signaling cascade. In addition, we observed transient preservation of transepithelial electrical resistance during the early stage of hypoxia (1% O(2)) as well as enhanced transepithelial electrical resistance recovery after prolonged hypoxia in SUMO-1-expressing cell monolayers. In conclusion, our results unveil a previously unrecognized mechanism by which SUMOylation and activation of ataxia-telangiectasia-mutated protein, PKCdelta, caspase-3, and nuclear factor kappaB signaling pathways modulate salivary adaptive responses to stress in cells exposed to either 1% O(2) or DFO.

Publication types

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

MeSH terms

  • Actins / metabolism
  • Animals
  • Ataxia Telangiectasia Mutated Proteins
  • Caspase 3
  • Caspases / metabolism
  • Cell Cycle Proteins / metabolism
  • Cell Hypoxia / physiology*
  • Cell Line
  • Cell Survival / drug effects
  • DNA-Binding Proteins / metabolism
  • Deferoxamine*
  • Epithelial Cells / metabolism*
  • Epithelial Cells / physiology
  • Humans
  • Membrane Proteins / metabolism
  • NF-kappa B / metabolism
  • Phosphoproteins / metabolism
  • Protein Kinase C-delta / metabolism
  • Protein Serine-Threonine Kinases / metabolism
  • Rats
  • SUMO-1 Protein / metabolism*
  • SUMO-1 Protein / physiology
  • Salivary Glands / cytology*
  • Signal Transduction
  • Transfection
  • Tumor Suppressor Proteins / metabolism
  • Zonula Occludens-1 Protein

Substances

  • Actins
  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • Membrane Proteins
  • NF-kappa B
  • Phosphoproteins
  • SUMO-1 Protein
  • TJP1 protein, human
  • Tjp1 protein, rat
  • Tumor Suppressor Proteins
  • Zonula Occludens-1 Protein
  • Prkcd protein, rat
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins
  • Protein Serine-Threonine Kinases
  • Protein Kinase C-delta
  • CASP3 protein, human
  • Casp3 protein, rat
  • Caspase 3
  • Caspases
  • Deferoxamine