Abstract
Liver fatty acid-binding protein (L-FABP, FABP1) is a highly conserved key factor in lipid metabolism. This study was undertaken to verify whether the T94A mutation in the L-FABP gene affects fatty acid uptake and intracellular esterification into specific lipid pools. Candidate SNPs were recreated using site-directed mutagenesis and tested for physical function in stably transfected Chang liver cell lines. We found that the T94A mutant of L-FABP lowered FFA uptake but had no effect on FFA efflux. L-FABP T94A-expressing cells showed decreased triglyceride content and increased cholesterol accumulation compared to the wild-type control for cells incubated with an FFA mixture (oleate: palmitate, 2:1 ratio). In conclusion, our study provided additional indications of the functional relevance of the L-FABP T94A SNP in hepatic fatty acid and lipid metabolism in humans.
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Acknowledgments
This study was supported by the National Undergraduate Student Innovation Experimental Design Project (YA07048) and the Hunan Province Science and Technology Plan (2007FG3035).
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The authors report no conflicts of interest regarding this study.
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Gao, N., Qu, X., Yan, J. et al. L-FABP T94A decreased fatty acid uptake and altered hepatic triglyceride and cholesterol accumulation in Chang liver cells stably transfected with L-FABP. Mol Cell Biochem 345, 207–214 (2010). https://doi.org/10.1007/s11010-010-0574-7
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DOI: https://doi.org/10.1007/s11010-010-0574-7