Down-regulation of aldose reductase renders J774A.1 cells more susceptible to acrolein- or hydrogen peroxide-induced cell death
- Authors
- Kang, Eun Sil; Kim, Gil Hyeong; Woo, Im Sun; Kim, Hyo Jung; Eun, So Young; Ham, Sun Ah; Jin, Hana; Kim, Min Young; Park, Myung Hyun; Kim, Hye Jung; Chang, Ki Churl; Lee, Jae Heun; Kim, Jin-Hoi; Yabe-Nishimura, Chihiro; Seo, Han Geuk
- Issue Date
- Nov-2008
- Publisher
- TAYLOR & FRANCIS LTD
- Keywords
- Aldose reductase (AR); acrolein; hydrogen peroxide; oxidative stress; reactive oxygen species (ROS)
- Citation
- FREE RADICAL RESEARCH, v.42, no.11-12, pp 930 - 938
- Pages
- 9
- Indexed
- SCIE
SCOPUS
- Journal Title
- FREE RADICAL RESEARCH
- Volume
- 42
- Number
- 11-12
- Start Page
- 930
- End Page
- 938
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/27222
- DOI
- 10.1080/10715760802555593
- ISSN
- 1071-5762
1029-2470
- Abstract
- Aldose reductase (AR) is abundantly expressed in a variety of cell lineages and has been implicated in the cellular response against oxidative stress. However, the exact functional role of AR against oxidative stress remains relatively unclear. This study investigated the role of AR in acrolein- or hydrogen peroxide-induced apoptosis using the J774.A.1 macrophage cell line. Ablation of AR with a small interference RNA or inhibition of AR activity significantly enhanced the acrolein- or hydrogen peroxide-induced generation of reactive oxygen species and aldehydes, leading to increased apoptotic cell death. Blockade of AR activity in J774A.1 cells markedly augmented the acrolein- or hydrogen peroxide-induced translocation of Bax to mitochondria. along with reduced Bcl-2 and increased release of cytochrome c from the mitochodria. Taken together, these findings indicate that AR plays an important role in the cellular response against oxidative stress, by sequestering the reactive molecules generated in cells exposed to toxic substances.
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