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. 2018 Oct 6;59(12):2383–2396. doi: 10.1194/jlr.M090050

Fig. 7.

Fig. 7.

The elongation of AA-d8 and EPA-d5 following ELOVL5 knockdown in Jurkat cells, proliferating primary T-cells, and HepG2 cells. Jurkat cells (A), proliferating T-cells (B), and HepG2 cells (C) were transfected with NS control siRNA and siRNA against ELOVL5. Cells were incubated for 48 h in regular culture media before a 24 h supplementation with 5 µM AA-d8 or EPA-d5. Cellular lipids were extracted and hydrolyzed, and pentafluorobenzyl esters of FAs were prepared and measured by negative ion chemical ionization GC/MS. The values represent the percentage of the cellular AA-d8 and EPA-d5 that was elongated to 22:4-d8 and 22:5-d5, respectively. The results are means ± SEMs of three independent experiments. *Different from cells transfected with the NS siRNA (P < 0.05) as determined by paired two-sided Student’s t-test.