3,4‐dihydroxybenzalacetone and caffeic acid phenethyl ester induce preconditioning ER stress and autophagy in SH‐SY5Y cells

• Published in: Journal of cellular physiology 2018-02, Vol.233 (2), p.1671-1684
• Main Authors: Tomiyama, Ryoichi, Takakura, Ken, Takatou, Shouhei, Le, Thuong M., Nishiuchi, Takumi, Nakamura, Yutaka, Konishi, Tetsuya, Matsugo, Seiichi, Hori, Osamu
• Format: Article
• Language: English
• Subjects: 6-Hydroxydopamine; Acetylcysteine; Antioxidants; Autophagy; Autophagy - drug effects; Caffeic acid; Caffeic Acids - pharmacology; Catechol; Cell Line, Tumor; Deoxyribonucleic acid; DNA; DNA microarrays; Dose-Response Relationship, Drug; Endoplasmic reticulum; Endoplasmic Reticulum Stress - drug effects; Gene expression; Gene Expression Regulation - drug effects; Genes; GRP78 protein; Human behavior; Humans; Microtubule-Associated Proteins - genetics; Microtubule-Associated Proteins - metabolism; Neuroblasts; Neurons - drug effects; Neurons - metabolism; Neurons - pathology; Neuroprotective Agents - pharmacology; Neurotoxins; Oxidative stress; Oxidative Stress - drug effects; Oxidopamine - toxicity; Phagocytosis; Phenylbutyric acid; Phenylethyl Alcohol - analogs & derivatives; Phenylethyl Alcohol - pharmacology; Preconditioning; Pretreatment; Protein folding; Proteins; Signal Transduction - drug effects; Time Factors; Unfolded Protein Response - drug effects; UPR
• ISSN: 0021-9541; 1097-4652
• DOI: 10.1002/jcp.26080

3,4‐dihydroxybenzalacetone (DBL) and Caffeic acid phenethyl ester (CAPE) are both catechol‐containing phenylpropanoid derivatives with diverse bioactivities. In the present study, we analyzed the ability of these compounds to activate the unfolded protein response (UPR) and the oxidative stress response. When human SH‐SY5Y neuroblastoma cells were treated with DBL or CAPE, the expression of endoplasmic reticulum (ER) stress‐related genes such as HSPA5, HYOU1, DDIT3, and SEC61b increased to a larger extent in response to CAPE treatment, while that of antioxidant genes such as HMOX1, GCLM, and NQO1 increased to a larger extent in response to DBL treatment. DNA microarray analysis confirmed the strong link of these compounds to ER stress. Regarding the mechanism, activation of the UPR by these compounds was associated with enhanced levels of oxidized proteins in the ER, and N‐acetyl cysteine (NAC), which provides anti‐oxidative effects, suppressed the induction of the UPR‐target genes. Furthermore, both compounds enhanced the expression of LC3‐II, a marker of autophagy, and 4‐Phenylbutyric acid (4‐PBA), a chemical chaperone that reduces ER stress, suppressed it. Finally, pretreatment of cells with DBL, CAPE or low doses of ER stressors protected cells against a neurotoxin 6‐hydroxydopamine (6‐OHDA) in an autophagy‐dependent manner. These results suggest that DBL and CAPE induce oxidized protein‐mediated ER stress and autophagy that may have a preconditioning effect in SH‐SY5Y cells. 3,4‐dihydroxybenzalacetone (DBL) and Caffeic acid phenethyl ester (CAPE) are both catechol‐containing phenylpropanoid derivatives with diverse bioactivities. We demonstrate here that both compounds induce oxidized protein‐mediated ER stress and autophagy that may have a preconditioning effect in SH‐SY5Y cells.