DNA repair capacity varies greatly between individuals(Reference Wilson, Kim and Berquist1), and evidence has begun to link this variation to cancer risk, obesity and related chronic diseases(Reference Sampath, Vartanian and Rollins2). There is also emerging evidence that dietary components can affect DNA repair(Reference Collins, Azqueta and Langie3), but research to date has been restricted by methods for measuring DNA repair(Reference Nagel, Chaim and Samson4). This study made use of newly developed microplate-based assays for the direct determination of DNA repair enzyme activities. Lipid loading of the HepG2 human hepatocellular carcinoma cell line was employed as a model to test the hypothesis that hepatic steatosis affects DNA repair activity via induction of oxidative stress.
HepG2 cells were treated with palmitic acid (PA), oleic acid (OA) or vehicle for 24 hours before determining cell viability, intracellular lipid levels, and DNA repair enzyme activity (uracil DNA glycosylase (hUNG1) and 8-oxoguanine DNA glycosylase (hOGG1)). For the repair assays, oligonucleotides designed to form a hairpin loop with a 5′ fluorescein and a damaged base (uracil for hUNG1 assay or 8-oxoguanine for hOGG1 assay) within the double stranded region were bound to the surface of Nunc Immobiliser™ plates via a 3′ amino group. HepG2 nuclear extract or recombinant enzyme was incubated with each substrate, creating alkali-labile abasic sites (hUNG1) or single strand breaks (hOGG1). Following alkaline denaturation, enzyme activity was determined by quantifying the retained fluorescein.
Treatment with 400μM PA decreased cell viability to 61 % (P < 0·01 compared to vehicle) (Fig. 1A.). Intracellular lipid was significantly increased following treatment with 300μM and 400μM OA (P < 0·05 and P < 0·001, respectively), and 300μM and 400μM PA (P < 0·001 and P < 0·0001, respectively) compared to vehicle (Fig. 1B.). No differences in hUNG1 or hOGG1 activity were detected between treatment groups (Fig. 1C.).
In conclusion, fatty acid treatment reduced cell viability and increased intracellular lipid levels in a dose-dependent manner. The use of novel assays enabled quantitative determination of DNA repair enzyme activities in cell extracts. The absence of detectable effects of lipid loading on DNA repair could be due to the use of cancer cells as a model, which may be lacking certain DNA repair regulatory mechanisms normally present in healthy cells. Future work will focus on optimisation of the assays for use with primary cells samples from human volunteers.
This work was funded by a studentship awarded by the Biotechnology and Biological Sciences Research Council Doctoral Training Programme.