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Cited 9 time in webofscience Cited 9 time in scopus
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Down-regulation of aldose reductase renders J774A.1 cells more susceptible to acrolein- or hydrogen peroxide-induced cell death

Authors
Kang, Eun SilKim, Gil HyeongWoo, Im SunKim, Hyo JungEun, So YoungHam, Sun AhJin, HanaKim, Min YoungPark, Myung HyunKim, Hye JungChang, Ki ChurlLee, Jae HeunKim, Jin-HoiYabe-Nishimura, ChihiroSeo, 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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