Korean J Physiol Pharmacol.
1997 Apr;1(2):209-219.
Reduction of TNF alpha-induced oxidative DNA damage product,
8-hydroxy-2'-deoxyguanosine, in L929 cells stably transfected with
small heat shock protein
- Affiliations
-
- 1
Department of Chemistry, Inchon University College of Natural Sciences, 402-749 South Korea.
Abstract
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Previous studies have demonstrated that oxidative stress involving
generation of reactive oxygen species (ROS) is responsible for the
cytotoxic action of TNF alpha. Protective effect of small heat shock
proteins (small HSP) against diverse oxidative stress conditions has
been suggested. Although overexpression of small hsp was shown to
provide an enhanced survival of TNF alpha-sensitive cells when
challenged with TNF alpha, neither the nature of TNF alpha-induced
cytotoxicity nor the protective mechanism of small HSP has not been
completely understood. In this study, we have attempted to determine
whether TNF alpha induces oxidative DNA damage in TNF alpha-sensitive
L929 cells. We chose to measure the level of
8-hydroxy-2'-deoxyguanosine (8 ohdG), which has been increasingly
recognized as one of the most sensitive markers of oxidative DNA
damage. Our results clearly demonstrated that the level of 8 ohdG
increased in L929 cells in a TNF alpha dose-dependent manner.
Subsequently, we asked whether small HSP has a protective effect on TNF
alpha-induced oxidative DNA damage. To accomplish this goal, we have
stably transfected L929 cells with mouse small hsp cDNA (hsp25) since
these cells are devoid of endogenous small hsps. We found that TNF
alpha-induced 8 ohdG was decreased in cells overexpressing exogenous
small hsp. We also found that the cell killing activity of TNF alpha
was decreased in these cells as measured by clonogenic survival. Taken
together, results from the current study show that cytotoxic mechanism
of TNF alpha involves oxidative damage of DNA and that overexpression
of the small hsp reduces this oxidative damage. We suggest that the
reduction of oxidative DNA damage is one of the most important
protective mechanisms of small HSP against TNF alpha.