Adenoviral CCN Gene Transfers Induce in Vitro and in Vivo Endoplasmic Reticulum Stress and Unfolded Protein Response

Biochim Biophys Acta. 2016 Nov;1863(11):2604-2612. doi: 10.1016/j.bbamcr.2016.07.006. Epub 2016 Jul 22.

Abstract

The endoplasmic reticulum (ER) is primarily recognized as the site of synthesis and folding of secreted membrane-bound and certain organelle-targeted proteins. Optimum protein folding requires several factors, including ATP, Ca2+ and an oxidizing environment to allow disulphide-bond formation. ER is highly sensitive to stress that perturb cellular energy levels, the redox state or the Ca2+ concentration. Such stresses reduce the protein folding capacity of the ER, resulting in the accumulation and aggregation of unfolded proteins, a condition referred to as unfolded protein response (UPR). Matricellular proteins of the CCN (CYR61, CTGF, NOV) family play essential roles in extracellular matrix signaling and turnover. They exhibit a similar type of organization and share a closely related primary structure, including 38 conserved cysteine residues. Since CCN1/CYR61 overexpression in hepatic stellate cells (HSC) induces ER stress-related apoptosis, we endeavored to investigate whether the adenovirus mediated gene transfer of other members of CCN proteins incurs ER stress in primary HSC and hepatocytes. We found Ad5-CMV-CCN2, Ad5-CMV-CCN3 and Ad5-CMV-CCN4 to induce ER stress and UPR comparable to Ad5-CMV-CCN1. UPR is a pro-survival response to reduce accumulation of unfolded proteins and restore normal ER functioning. If, however protein aggregation is persistent and the stress cannot be resolved, signaling switches from pro-survival to pro-apoptosis. The observed CCN-induced UPR is relevant in wound healing responses and essential for hepatic tissue repair following liver injury. Adenoviral gene transfer induced massive amounts of matricellular proteins proving to effectively mitigate liver fibrosis if targeted cell specific in HSC and myofibroblasts.

Keywords: CCN proteins; ER stress; hepatic stellate cells; hepatocytes; matricellular proteins; unfolded protein response.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics*
  • Animals
  • Apoptosis
  • CCN Intercellular Signaling Proteins / genetics
  • CCN Intercellular Signaling Proteins / metabolism*
  • Cells, Cultured
  • Cellular Senescence
  • Endoplasmic Reticulum / metabolism*
  • Endoplasmic Reticulum / pathology
  • Endoplasmic Reticulum Stress*
  • Genetic Vectors*
  • Hepatic Stellate Cells / metabolism
  • Hepatic Stellate Cells / pathology
  • Hepatocytes / metabolism
  • Hepatocytes / pathology
  • Liver / metabolism*
  • Liver / pathology
  • Liver Cirrhosis, Experimental / etiology
  • Liver Cirrhosis, Experimental / genetics
  • Liver Cirrhosis, Experimental / metabolism*
  • Liver Cirrhosis, Experimental / pathology
  • Male
  • Mice, Inbred C57BL
  • Myofibroblasts / metabolism
  • Myofibroblasts / pathology
  • Protein Aggregates
  • Rats, Sprague-Dawley
  • Signal Transduction
  • Transduction, Genetic*
  • Transfection / methods*
  • Unfolded Protein Response*

Substances

  • CCN Intercellular Signaling Proteins
  • Protein Aggregates