| Literature DB >> 26855420 |
Yantao Duan1, Yaohui Gao2, Jun Zhang1, Yinan Chen1, Yannan Jiang1, Jun Ji1, Jianian Zhang1, Xuehua Chen1, Qiumeng Yang1, Liping Su1, Jun Zhang1, Bingya Liu1, Zhenggang Zhu3, Lishun Wang4, Yingyan Yu5.
Abstract
Mitochondrial aldehyde dehydrogenase 2 (ALDH2) is a member of the aldehyde dehydrogenase superfamily and is involved with the metabolic processing of aldehydes. ALDH2 plays a cytoprotective role by removing aldehydes produced during normal metabolism. We examined the cytoprotective role of ALDH2 specifically in gastric mucosa cells. Overexpression of ALDH2 increased the viability of gastric mucosa cells treated with H2O2, while knockdown of ALDH2 had an opposite effect. Moreover, overexpression of ALDH2 protected gastric mucosa cells against oxidative stress-induced apoptosis as determined by flow cytometry, Hoechst 33342, and TUNEL assays. Consistently, ALDH2 knockdown had an opposite effect. Additionally, DNA damage was ameliorated in ALDH2-overexpressing gastric mucosa cells treated with H2O2. We further identified that this cytoprotective role of ALDH2 was mediated by metabolism of 4-hydroxynonenal (4-HNE). Consistently, 4-HNE mimicked the oxidative stress induced by H2O2 in gastric mucosa cells. Treatment with 4-HNE increased levels of DNA damage in ALDH2-knockdown GES-1 cells, while overexpression of ALDH2 decreased 4-HNE-induced DNA damage. These findings suggest that ALDH2 can protect gastric mucosa cells against DNA damage caused by oxidative stress by reducing levels of 4-HNE.Entities:
Keywords: 4-Hydroxynonenal; ALDH2; Apoptosis; DNA damage; Oxidative stress
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Year: 2016 PMID: 26855420 DOI: 10.1016/j.freeradbiomed.2016.02.001
Source DB: PubMed Journal: Free Radic Biol Med ISSN: 0891-5849 Impact factor: 7.376