Proteasome dysfunction mediates high glucose-induced apoptosis in rodent beta cells and human islets

PLoS One. 2014 Mar 18;9(3):e92066. doi: 10.1371/journal.pone.0092066. eCollection 2014.

Abstract

The ubiquitin/proteasome system (UPS), a major cellular protein degradation machinery, plays key roles in the regulation of many cell functions. Glucotoxicity mediated by chronic hyperglycaemia is detrimental to the function and survival of pancreatic beta cells. The aim of our study was to determine whether proteasome dysfunction could be involved in beta cell apoptosis in glucotoxic conditions, and to evaluate whether such a dysfunction might be pharmacologically corrected. Therefore, UPS activity was measured in GK rats islets, INS-1E beta cells or human islets after high glucose and/or UPS inhibitor exposure. Immunoblotting was used to quantify polyubiquitinated proteins, endoplasmic reticulum (ER) stress through CHOP expression, and apoptosis through the cleavage of PARP and caspase-3, whereas total cell death was detected through histone-associated DNA fragments measurement. In vitro, we found that chronic exposure of INS-1E cells to high glucose concentrations significantly decreases the three proteasome activities by 20% and leads to caspase-3-dependent apoptosis. We showed that pharmacological blockade of UPS activity by 20% leads to apoptosis in a same way. Indeed, ER stress was involved in both conditions. These results were confirmed in human islets, and proteasome activities were also decreased in hyperglycemic GK rats islets. Moreover, we observed that a high glucose treatment hypersensitized beta cells to the apoptotic effect of proteasome inhibitors. Noteworthily, the decreased proteasome activity can be corrected with Exendin-4, which also protected against glucotoxicity-induced apoptosis. Taken together, our findings reveal an important role of proteasome activity in high glucose-induced beta cell apoptosis, potentially linking ER stress and glucotoxicity. These proteasome dysfunctions can be reversed by a GLP-1 analog. Thus, UPS may be a potent target to treat deleterious metabolic conditions leading to type 2 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Apoptosis / genetics*
  • Caspase 3 / genetics
  • Caspase 3 / metabolism
  • Cells, Cultured
  • Endoplasmic Reticulum Stress / drug effects
  • Endoplasmic Reticulum Stress / genetics
  • Exenatide
  • Gene Expression
  • Glucose / metabolism
  • Glucose / pharmacology*
  • Humans
  • Hyperglycemia / genetics
  • Hyperglycemia / metabolism*
  • Hyperglycemia / pathology
  • Hypoglycemic Agents / pharmacology
  • Insulin-Secreting Cells / drug effects
  • Insulin-Secreting Cells / metabolism*
  • Insulin-Secreting Cells / pathology
  • Male
  • Peptides / pharmacology
  • Poly(ADP-ribose) Polymerases / genetics
  • Poly(ADP-ribose) Polymerases / metabolism
  • Proteasome Endopeptidase Complex / drug effects
  • Proteasome Endopeptidase Complex / metabolism*
  • Proteasome Inhibitors / pharmacology
  • Proteolysis / drug effects
  • Rats
  • Signal Transduction
  • Transcription Factor CHOP / genetics
  • Transcription Factor CHOP / metabolism
  • Ubiquitin / genetics
  • Ubiquitin / metabolism
  • Venoms / pharmacology

Substances

  • DDIT3 protein, human
  • Ddit3 protein, rat
  • Hypoglycemic Agents
  • Peptides
  • Proteasome Inhibitors
  • Ubiquitin
  • Venoms
  • Transcription Factor CHOP
  • Exenatide
  • Poly(ADP-ribose) Polymerases
  • Caspase 3
  • Proteasome Endopeptidase Complex
  • Glucose

Grants and funding

This work was supported by grants obtained from the following: the Société Francophone du Diabète (SFD) bourse ALFEDIAM-Industrie; the Agence de Biomedecine bourse AOR Recherche et Greffe; the Institut National de la Santé et de la Recherche Médicale (INSERM, Paris, France); and the Région Languedoc-Roussillon, France. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.