Death Protein 5 and p53-Upregulated Modulator of Apoptosis Mediate the Endoplasmic Reticulum Stress-Mitochondrial Dialog Triggering Lipotoxic Rodent and Human β-Cell Apoptosis

Autor: Lorella Marselli, Daniel Andrade Da Cunha, Chantal Mathieu, Conny Gysemans, Decio L. Eizirik, Najib Naamane, Piero Marchetti, David Ron, Carla Maria Ramos C.M. Germano, Jean-Marie Vanderwinden, Mariana Igoillo-Esteve, Esteban Nicolas Gurzov, Ihsane Marhfour, Makiko Fukaya, Heather P. Harding, Miriam Cnop
Jazyk: angličtina
Rok vydání: 2012
Předmět:
Male
Endocrinology
Diabetes and Metabolism

Palmitic Acid
Proto-Oncogene Proteins -- antagonists & inhibitors -- genetics -- metabolism
Apoptosis
Mitochondrion
ACTIVATION
Mice
Mitochondria -- metabolism
Puma
Insulin-Secreting Cells
Insulin-Secreting Cells -- cytology -- metabolism
RNA
Small Interfering

Cells
Cultured

Mice
Knockout

biology
FREE FATTY-ACIDS
Sciences bio-médicales et agricoles
Middle Aged
ER STRESS
Endoplasmic Reticulum Stress
Cell biology
Mitochondria
RNA Interference
Life Sciences & Biomedicine
Signal Transduction
medicine.medical_specialty
Programmed cell death
KAPPA-B
Cell Line
CONTRIBUTES
Endocrinology & Metabolism
Internal medicine
Proto-Oncogene Proteins
SELECTIVE-INHIBITION
PUMA
Internal Medicine
medicine
Animals
Humans
p53 upregulated modulator of apoptosis
RNA
Messenger

Protein kinase B
INDUCIBLE GENE
Aged
Science & Technology
Endoplasmic reticulum
Palmitic Acid -- adverse effects
Gene Expression Profiling
JNK PHOSPHORYLATION
biology.organism_classification
RNA
Messenger -- metabolism

Rats
Mice
Inbred C57BL

Endocrinology
DEPENDENT APOPTOSIS
biology.protein
Unfolded protein response
Apoptosis Regulatory Proteins
Apoptosis Regulatory Proteins -- antagonists & inhibitors -- genetics -- metabolism
Zdroj: Diabetes
Diabetes (New York, N.Y.), 61 (11
Popis: Environmental factors such as diets rich in saturated fats contribute to dysfunction and death of pancreatic β-cells in diabetes. Endoplasmic reticulum (ER) stress is elicited in β-cells by saturated fatty acids. Here we show that palmitate-induced β-cell apoptosis is mediated by the intrinsic mitochondrial pathway. By microarray analysis, we identified a palmitate-triggered ER stress gene expression signature and the induction of the BH3-only proteins death protein 5 (DP5) and p53-upregulated modulator of apoptosis (PUMA). Knockdown of either protein reduced cytochrome c release, caspase-3 activation, and apoptosis in rat and human β-cells. DP5 induction depends on inositol-requiring enzyme 1 (IRE1)-dependent c-Jun NH₂-terminal kinase and PKR-like ER kinase (PERK)-induced activating transcription factor (ATF3) binding to its promoter. PUMA expression is also PERK/ATF3-dependent, through tribbles 3 (TRB3)-regulated AKT inhibition and FoxO3a activation. DP5(-/-) mice are protected from high fat diet-induced loss of glucose tolerance and have twofold greater pancreatic β-cell mass. This study elucidates the crosstalk between lipotoxic ER stress and the mitochondrial pathway of apoptosis that causes β-cell death in diabetes.
info:eu-repo/semantics/published
Databáze: OpenAIRE