Genetics
Suppressing CETP synthesis in fat cells causes cholesteryl ester to pile up threefold by blocking its normal mobilization (J Biol Chem 2001)
Original title: Cholesteryl ester transfer protein biosynthesis and cellular cholesterol homeostasis are tightly interconnected
This study used the SW872 adipocytic cell line, which secretes CETP at higher levels than Caco-2 or HepG2 cells, to investigate CETP synthesis regulation and its relationship to cellular lipid metabolism. Adding LDL, 25OH-cholesterol, oleic acid, or acetylated LDL increased CETP secretion up to 6-fold, while lipoprotein-deficient serum or beta-cyclodextrin decreased CETP production by almost 60%, paralleled by changes in CETP mRNA. Suppressing CETP synthesis with antisense oligonucleotides reduced CETP secretion by 60%; after 24 hours, triglyceride synthesis was unchanged but cholesterol biosynthesis fell 20% and acetate incorporation into cholesteryl ester (CE) rose 31%, growing to a 3-fold increase in CE incorporation and matching CE mass increase after 3 days. Free cholesterol efflux to HDL was unchanged, but HDL-induced CE hydrolysis was diminished 2-fold despite unchanged neutral CE hydrolase activity. The authors conclude CETP-compromised cells show inefficient CE mobilization leading to CE accumulation, demonstrating that CETP expression and cellular lipid homeostasis are tightly coupled.
Original abstract
Cholesteryl ester transfer protein (CETP) mediates triglyceride and cholesteryl ester (CE) transfer between lipoproteins, and its activity is strongly modulated by dietary cholesterol. To better understand the regulation of CETP synthesis and the relationship between CETP levels and cellular lipid metabolism, we selected the SW872 adipocytic cell line as a model. These cells secrete CETP in a time-dependent manner at levels exceeding those observed for Caco-2 or HepG2 cells. The addition of LDL, 25OH-cholesterol, oleic acid, or acetylated LDL to SW872 cells increased CETP secretion (activity and mass) up to 6-fold. In contrast, CETP production was decreased by almost 60% after treatment with lipoprotein-deficient serum or beta-cyclodextrin. These effects, which were paralleled by changes in CETP mRNA, show that CETP biosynthesis in SW872 cells directly correlates with cellular lipid status. To investigate a possible, reciprocal relationship between CETP expression and cellular lipid homeostasis, CETP biosynthesis in SW872 cells was suppressed with CETP antisense oligonucleotides. Antisense oligonucleotides reduced CETP secretion (activity and mass) by 60% compared with sense-treated cells. When CETP synthesis was suppressed for 24 h, triglyceride synthesis was unchanged, but cholesterol biosynthesis was reduced by 20%, and acetate incorporation into CE increased 31%. After 3 days of suppressed CETP synthesis, acetate incorporation into the CE pool increased 3-fold over control. This mirrored a similar increase in CE mass. The efflux of free cholesterol to HDL was the same in sense and antisense-treated cells; however, HDL-induced CE hydrolysis in antisense-treated cells was diminished 2-fold even though neutral CE hydrolase activity was unchanged. Thus, CETP-compromised SW872 cells display a phenotype characterized by inefficient mobilization of CE stores leading to CE accumulation. These results strongly suggest that CETP expression levels contribute to normal cholesterol homeostasis in adipocytic cells. Overall, these studies demonstrate that lipid homeostasis and CETP expression are tightly coupled.
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.