Alcohol disrupts endoplasmic reticulum function and protein secretion in hepatocytes

Deanna L. Howarth, Ana M. Vacaru, Orkhontuya Tsedensodnom, Elisabetta Mormone, Natalia Nieto, Lindsey M. Costantini, Erik L. Snapp, Kirsten Sadler Edepli

Research output: Contribution to journalArticle

Abstract

Background: Many alcoholic patients have serum protein deficiency that contributes to their systemic problems. The unfolded protein response (UPR) is induced in response to disequilibrium in the protein folding capability of the endoplasmic reticulum (ER) and is implicated in hepatocyte lipid accumulation and apoptosis, which are associated with alcoholic liver disease (ALD). We investigated whether alcohol affects ER structure, function, and UPR activation in hepatocytes in vitro and in vivo. Methods: HepG2 cells expressing human cytochrome P450 2E1 and mouse alcohol dehydrogenase (VL-17A) were treated for up to 48hours with 50 and 100mM ethanol. Zebrafish larvae at 4days postfertilization were exposed to 350mM ethanol for 32hours. ER morphology was visualized by fluorescence in cells and transmission electron microscopy in zebrafish. UPR target gene activation was assessed using quantitative PCR, in situ hybridization, and Western blotting. Mobility of the major ER chaperone, BIP, was monitored in cells by fluorescence recovery after photobleaching (FRAP). Results: VL-17A cells metabolized alcohol yet only had slight activation of some UPR target genes following ethanol treatment. However, ER fragmentation, crowding, and accumulation of unfolded proteins as detected by immunofluorescence and FRAP demonstrate that alcohol induced some ER dysfunction despite the lack of UPR activation. Zebrafish treated with alcohol, however, showed modest ER dilation, and several UPR targets were significantly induced. Conclusions: Ethanol metabolism directly impairs ER structure and function in hepatocytes. Zebrafish are a novel in vivo system for studying ALD.

Original languageEnglish (US)
Pages (from-to)14-23
Number of pages10
JournalAlcoholism: Clinical and Experimental Research
Volume36
Issue number1
DOIs
StatePublished - Jan 1 2012

Fingerprint

Unfolded Protein Response
Endoplasmic Reticulum
Hepatocytes
Alcohols
Zebrafish
Ethanol
Chemical activation
Proteins
Photobleaching
Fluorescence Recovery After Photobleaching
Fluorescence
Alcoholic Liver Diseases
Liver
Genes
Protein folding
Recovery
Cytochrome P-450 CYP2E1
Alcohol Dehydrogenase
Protein Deficiency
Protein Unfolding

Keywords

  • Alcoholic Liver Disease
  • Ethanol
  • Fluorescence Recovery After Photobleaching
  • Liver
  • Unfolded Protein Response
  • Zebrafish

ASJC Scopus subject areas

  • Medicine (miscellaneous)
  • Toxicology
  • Psychiatry and Mental health

Cite this

Alcohol disrupts endoplasmic reticulum function and protein secretion in hepatocytes. / Howarth, Deanna L.; Vacaru, Ana M.; Tsedensodnom, Orkhontuya; Mormone, Elisabetta; Nieto, Natalia; Costantini, Lindsey M.; Snapp, Erik L.; Sadler Edepli, Kirsten.

In: Alcoholism: Clinical and Experimental Research, Vol. 36, No. 1, 01.01.2012, p. 14-23.

Research output: Contribution to journalArticle

Howarth, Deanna L. ; Vacaru, Ana M. ; Tsedensodnom, Orkhontuya ; Mormone, Elisabetta ; Nieto, Natalia ; Costantini, Lindsey M. ; Snapp, Erik L. ; Sadler Edepli, Kirsten. / Alcohol disrupts endoplasmic reticulum function and protein secretion in hepatocytes. In: Alcoholism: Clinical and Experimental Research. 2012 ; Vol. 36, No. 1. pp. 14-23.
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