Palmitate-induced Endoplasmic Reticulum stress and subsequent C/EBPα Homologous Protein activation attenuates leptin and Insulin-like growth factor 1 expression in the brain

Gurdeep Marwarha, Kate Claycombe, Jared Schommer, David Collins, Othman Ghribi

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

The peptide hormones Insulin-like growth factor-1 (IGF1) and leptin mediate a myriad of biological effects - both in the peripheral and central nervous systems. The transcription of these two hormones is regulated by the transcription factor C/EBPα, which in turn is negatively regulated by the transcription factor C/EBP Homologous Protein (CHOP), a specific marker of endoplasmic reticulum (ER) stress. In the peripheral system, disturbances in leptin and IGF-1 levels are implicated in a variety of metabolic diseases including obesity, diabetes, atherosclerosis and cardiovascular diseases. Current research suggests a positive correlation between consumption of diets rich in saturated free fatty acids (sFFA) and metabolic diseases. Induction of ER stress and subsequent dysregulation in the expression levels of leptin and IGF-1 have been shown to mediate sFFA-induced metabolic diseases in the peripheral system. Palmitic acid (palmitate), the most commonly consumed sFFA, has been shown to be up-taken by the brain, where it may promote neurodegeneration. However, the extent to which palmitate induces ER stress in the brain and attenuates leptin and IGF1 expression has not been determined. We fed C57BL/6J mice a palmitate-enriched diet and determined effects on the expression levels of leptin and IGF1 in the hippocampus and cortex. We further determined the extent to which ER stress and subsequent CHOP activation mediate the palmitate effects on the transcription of leptin and IGF1. We demonstrate that palmitate induces ER stress and decreases leptin and IGF1 expression by inducing the expression of CHOP. The molecular chaperone 4-phenylbutyric acid (4-PBA), an inhibitor of ER stress, precludes the palmitate-evoked down-regulation of leptin and IGF1 expression. Furthermore, the activation of CHOP in response to ER stress is pivotal in the attenuation of leptin and IGF1 expression as knocking-down CHOP in mice or in SH-SY5Y and Neuro-2a (N2a) cells rescues the palmitate-induced mitigation in leptin and IGF1 expression. Our study implicates for the first time ER stress-induced CHOP activation in the brain as a mechanistic link in the palmitate-induced negative regulation of leptin and IGF1, two neurotrophic cytokines that play an indispensable role in the mammalian brain.

Original languageEnglish (US)
Pages (from-to)1789-1805
Number of pages17
JournalCellular Signalling
Volume28
Issue number11
DOIs
StatePublished - Nov 1 2016

Fingerprint

Transcription Factor CHOP
Endoplasmic Reticulum Stress
Palmitates
Somatomedins
Leptin
Brain
Metabolic Diseases
Nonesterified Fatty Acids
Fatty Acids
Insulin-Like Growth Factor I
Transcription Factors
Diet
Molecular Chaperones
Palmitic Acid
Peptide Hormones
Peripheral Nervous System
Inbred C57BL Mouse
Hippocampus

Keywords

  • C/EBP Homologous Protein
  • CCAAT Enhancer Binding Protein alpha
  • Endoplasmic Reticulum stress
  • Insulin-like growth factor 1
  • Leptin
  • Palmitic acid

ASJC Scopus subject areas

  • Cell Biology

Cite this

Palmitate-induced Endoplasmic Reticulum stress and subsequent C/EBPα Homologous Protein activation attenuates leptin and Insulin-like growth factor 1 expression in the brain. / Marwarha, Gurdeep; Claycombe, Kate; Schommer, Jared; Collins, David; Ghribi, Othman.

In: Cellular Signalling, Vol. 28, No. 11, 01.11.2016, p. 1789-1805.

Research output: Contribution to journalArticle

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