Skip to main content
. 2015 Mar;56(3):515–525. doi: 10.1194/jlr.M053678

TABLE 3.

Sterol metabolism in native and CETP+ cells

Relative mRNA level
Cell CE content CE synthesis CE hydrolysis HMGCR ABCG1
Control 2.81 ± 0.41 0.22 ± 0.07 23.0 ± 1.0 1.07 ± 0.08 1.06 ± 0.07
CETP+ 1.93 ± 0.31a 0.33 ± 0.03b 59.1 ± 10.3b 2.59 ± 0.35b 0.01 ± 0.01b

CE content was determined from the steady-state level of 3H-CE after 48 h incubation with 200 µM 3H-oleate/BSA. CE synthesis rates were determined from the slope of the 3H-CE accumulation curve over 4 h. To measure CE hydrolysis, after cells were incubated with 3H-oleate/BSA for 48 h, the decay in the 3H-CE pool was measured after oleate removal and the addition of HDL and BSA to the media. Gene expression for HMGCR (HMG-CoA reductase) and ABCG1 was measured by qPCR. Units are CE content, nmol/mg protein (n = 3); CE synthetic rate, nmol/mg protein/h (n = 6); CE hydrolysis, % decrease in CE pool over 8 h period (n = 2–3).

a

P < 0.05 versus control.

b

P < 0.01 versus control.