Inhibition of Foxo1 mediates protective effects of ghrelin against lipotoxicity in MIN6 pancreatic beta-cells

Peptides. 2010 Feb;31(2):307-14. doi: 10.1016/j.peptides.2009.11.011. Epub 2009 Nov 26.

Abstract

Ghrelin is a 28-amino-acid peptide secreted predominantly by X/A-like cells of the gastric fundus. Ghrelin increases pancreatic beta-cell proliferation and survival via sequential activation of phosphatidylinositol-3 kinase (PI3K) and Akt. The transcription regulator Foxo1 is a prominent effector of PI3K/Akt; when it is inhibited, pancreatic beta-cells are protected against fatty-acid-induced apoptosis. We investigated the role of Foxo1 in the protective effect of ghrelin under lipotoxic conditions in the MIN6 pancreatic beta-cell line. Results showed that ghrelin promoted cell proliferation and attenuated palmitate-induced apoptosis in cultured MIN6 cells. Nuclear exclusion of Foxo1 was necessary for the function of ghrelin. Treatment of MIN6 cells with palmitate and ghrelin-induced rapid nuclear exclusion and phosphorylation of Foxo1. Unlike the JNK inhibitor SP600125, Akt inhibitor IV blocked the anti-lipotoxic effect of ghrelin and stimulated Foxo1 nuclear translocation. In addition, treatment with ghrelin combined with SP600125 showed a synergistic antiapoptotic effect in palmitate-treated MIN6 cells. Ghrelin also inhibited the endoplasmic reticulum stress pathway of apoptosis in MIN6 cells, decreased expression of cytoplasmic triglyceride, and downregulated gene expression of Bcl-2-associated X (BAX), sterol-response element-binding protein 1c (SREBP1c), and C/EBP homologous protein (CHOP-10). These findings suggest that ghrelin protects pancreatic beta-cells from lipotoxicity by inhibiting the nuclear translocation of Foxo1.

MeSH terms

  • Animals
  • Anthracenes / pharmacology
  • Apoptosis / drug effects
  • Caspase 3 / metabolism
  • Cell Line
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Cell Proliferation / drug effects
  • Cytoplasm / drug effects
  • Cytoplasm / metabolism
  • Endoplasmic Reticulum / metabolism
  • Forkhead Box Protein O1
  • Forkhead Transcription Factors / metabolism*
  • Gene Expression / drug effects
  • Gene Expression / genetics
  • Ghrelin / pharmacology*
  • Insulin-Secreting Cells / drug effects
  • Insulin-Secreting Cells / metabolism*
  • JNK Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • Lipid Metabolism / drug effects
  • Lipid Metabolism / physiology*
  • Mice
  • Palmitic Acid / pharmacology
  • Phosphorylation / drug effects
  • Protein Kinase Inhibitors / pharmacology
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Serum Albumin, Bovine / pharmacology
  • Sterol Regulatory Element Binding Protein 1 / genetics
  • Stress, Physiological / drug effects
  • Stress, Physiological / physiology*
  • Transcription Factor CHOP / genetics
  • Triglycerides / metabolism
  • bcl-2-Associated X Protein / genetics

Substances

  • Anthracenes
  • Bax protein, mouse
  • Ddit3 protein, mouse
  • Forkhead Box Protein O1
  • Forkhead Transcription Factors
  • Foxo1 protein, mouse
  • Ghrelin
  • Protein Kinase Inhibitors
  • Srebf1 protein, mouse
  • Sterol Regulatory Element Binding Protein 1
  • Triglycerides
  • bcl-2-Associated X Protein
  • Transcription Factor CHOP
  • pyrazolanthrone
  • Serum Albumin, Bovine
  • Palmitic Acid
  • Proto-Oncogene Proteins c-akt
  • JNK Mitogen-Activated Protein Kinases
  • Caspase 3