Resveratrol, an activator of SIRT1, improves ER stress by increasing clusterin expression in HepG2 cells

• Published in: Cell stress & chaperones 2019-07, Vol.24 (4), p.825-833
• Main Authors: Lee, Jinmi, Hong, Seok-Woo, Kwon, Hyemi, Park, Se Eun, Rhee, Eun-Jung, Park, Cheol-Young, Oh, Ki-Won, Park, Sung-Woo, Lee, Won-Young
• Format: Article
• Language: English
• Subjects: Apoptosis; Autophagy; Autophagy - drug effects; Biochemistry; Biomarkers - metabolism; Biomedical and Life Sciences; Biomedicine; Cancer Research; Cell Biology; Cell death; Clusterin; Clusterin - metabolism; Conditioning; Endoplasmic reticulum; Endoplasmic Reticulum - metabolism; Endoplasmic Reticulum Stress - drug effects; Fatty liver; Gene expression; Hep G2 Cells; Humans; Immunology; Lipid metabolism; Lipids; mRNA; Neurosciences; Original Paper; Phagocytosis; Proteins; Proteins - metabolism; Resveratrol; Resveratrol - pharmacology; siRNA; SIRT1 protein; Sirtuin 1 - metabolism; Steatosis; Stress; Tunicamycin; Tunicamycin - pharmacology; Ubiquitin-Protein Ligases - metabolism
• ISSN: 1355-8145; 1466-1268
• DOI: 10.1007/s12192-019-01012-z

Endoplasmic reticulum stress (ER stress) is involved in lipid metabolism and lipotoxicity and can lead to apoptosis. Resveratrol, a sirtuin 1 (SIRT1) agonist, prevents ER stress and improves ER stress-induced hepatic steatosis and cell death. Clusterin is a secreted chaperone and has roles in various physiological processes. However, changes in the expression of clusterin upon ER stress and the connection between SIRT1 and clusterin in protection against ER stress are not well known. In cells treated with tunicamycin, resveratrol increased the expression of clusterin mRNA and protein and the secreted clusterin protein level in conditioned medium. Resveratrol decreased protein expression of the ER stress markers, p-PERK, p-IRElα, and CHOP, and increased the expression of the ER-associated degradation (ERAD) factors, SEL1L and HRD1, in tunicamycin-treated cells. However, no changes in the expression of these genes were observed in clusterin siRNA-transfected cells. Moreover, increased LAMP2 and LC3 expression and decreased Rubicon expression were observed in cells treated with resveratrol or secreted clusterin. These data suggest that SIRT1 activation by resveratrol attenuates ER stress by promoting protective processes such as ERAD and autophagy pathways and that these protective effects are mediated by clusterin.