ACSL3 and GSK-3β are essential for lipid upregulation induced by endoplasmic reticulum stress in liver cells

Yung Sheng Chang, Chien Ting Tsai, Chien An Huangfu, Wen Ya Huang, Huan Yao Lei, Chiou Feng Lin, Ih Jen Su, Wen Tsan Chang, Pei Huan Wu, Ya Ting Chen, Jui Hsiang Hung, Kung Chia Young, Ming Derg Lai

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

The endoplasmic reticulum (ER) is essential for lipid biosynthesis, and stress signals in this organelle are thought to alter lipid metabolism. Elucidating the mechanisms that underlie the dysregulation of lipid metabolism in hepatocytes may lead to novel therapeutic approaches for the treatment of lipid accumulation. We first tested the effects of several inhibitors on lipid dysregulation induced by tunicamycin, an ER stress inducer. Triacsin C, an inhibitor of long-chain acyl-CoA synthetase (ACSL) 1, 3, and 4, was the most potent among these inhibitors. We then analyzed the expression of the ACSL family during ER stress. The expression of ACSL3 was induced by ER stress in HuH-7 cells and in mice livers. ACSL3 shRNA, but not ACSL1 shRNA, inhibited the induction of lipid accumulation. GSK-3β inhibitors attenuated ACSL3 expression and the lipid accumulation induced by ER stress in HuH-7 cells. shRNA that target GSK-3β also inhibited the upregulation of ACSL3 and lipid accumulation in HuH-7 and HepG2 cells. The hepatitis B virus mutant large surface protein, which is known to induce ER stress, increased the lipid content of cells. Similarly, Triacsin C, and GSK-3β inhibitors abrogated the lipid dysregulation caused by the hepatitis B virus mutant large surface protein. Altogether, ACSL3 and GSK-3β represent novel therapeutic targets for lipid dysregulation by ER stress.

Original languageEnglish
Pages (from-to)881-893
Number of pages13
JournalJournal of Cellular Biochemistry
Volume112
Issue number3
DOIs
Publication statusPublished - Mar 2011
Externally publishedYes

Fingerprint

Glycogen Synthase Kinase 3
Endoplasmic Reticulum Stress
Liver
Up-Regulation
Lipids
Small Interfering RNA
Viruses
Lipid Metabolism
Membrane Proteins
Coenzyme A Ligases
Tunicamycin
Acyl Coenzyme A
Biosynthesis
Hep G2 Cells
Endoplasmic Reticulum
Organelles
Hepatocytes

Keywords

  • ACSL3
  • Endoplasmic reticulum stress
  • GSK-3beta
  • Lipid dysregulation

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Molecular Biology

Cite this

ACSL3 and GSK-3β are essential for lipid upregulation induced by endoplasmic reticulum stress in liver cells. / Chang, Yung Sheng; Tsai, Chien Ting; Huangfu, Chien An; Huang, Wen Ya; Lei, Huan Yao; Lin, Chiou Feng; Su, Ih Jen; Chang, Wen Tsan; Wu, Pei Huan; Chen, Ya Ting; Hung, Jui Hsiang; Young, Kung Chia; Lai, Ming Derg.

In: Journal of Cellular Biochemistry, Vol. 112, No. 3, 03.2011, p. 881-893.

Research output: Contribution to journalArticle

Chang, YS, Tsai, CT, Huangfu, CA, Huang, WY, Lei, HY, Lin, CF, Su, IJ, Chang, WT, Wu, PH, Chen, YT, Hung, JH, Young, KC & Lai, MD 2011, 'ACSL3 and GSK-3β are essential for lipid upregulation induced by endoplasmic reticulum stress in liver cells', Journal of Cellular Biochemistry, vol. 112, no. 3, pp. 881-893. https://doi.org/10.1002/jcb.22996
Chang, Yung Sheng ; Tsai, Chien Ting ; Huangfu, Chien An ; Huang, Wen Ya ; Lei, Huan Yao ; Lin, Chiou Feng ; Su, Ih Jen ; Chang, Wen Tsan ; Wu, Pei Huan ; Chen, Ya Ting ; Hung, Jui Hsiang ; Young, Kung Chia ; Lai, Ming Derg. / ACSL3 and GSK-3β are essential for lipid upregulation induced by endoplasmic reticulum stress in liver cells. In: Journal of Cellular Biochemistry. 2011 ; Vol. 112, No. 3. pp. 881-893.
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AU - Lei, Huan Yao

AU - Lin, Chiou Feng

AU - Su, Ih Jen

AU - Chang, Wen Tsan

AU - Wu, Pei Huan

AU - Chen, Ya Ting

AU - Hung, Jui Hsiang

AU - Young, Kung Chia

AU - Lai, Ming Derg

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