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HDL biology

CETP-mediated cholesteryl ester and triglyceride transfer in plasma is not an equimolar exchange (J Lipid Res 1995)

Original title: Neutral lipid mass transfer among lipoproteins in plasma from normolipidemic subjects is not an equimolar heteroexchange

J Lipid Res · · 7

Liu XQ, Bagdade JD

Net mass transfer of core lipids between lipoproteins was measured in intact plasma from ten healthy normolipidemic subjects to characterize CETP-mediated neutral lipid redistribution. Cholesteryl ester loss from HDL3 (19.5 nmol/ml/h) rose linearly over 6 hours (P < 0.01), with about 50% of transferred cholesteryl ester (118.7 nmol/ml total) going to VLDL, roughly 30% to LDL, and roughly 20% to HDL2. Triglyceride loss from VLDL (14.5 nmol/ml/h) also rose linearly (P < 0.01), with about 50% of transferred triglyceride (85.2 nmol/ml total) going to LDL, roughly 10% to HDL2, and roughly 40% to HDL3. Since the moles of cholesteryl ester lost from HDL3 were almost three times the moles of triglyceride it acquired, and HDL3 continued donating cholesteryl ester to LDL and HDL2 even without VLDL present (17.5 versus 20.2 nmol/ml/h in intact plasma) without accepting any triglyceride, the authors conclude that CETP-mediated cholesteryl ester and triglyceride transfer follow independent pathways rather than an obligatory equimolar heteroexchange.

PubMed

Original abstract

To further characterize the cholesteryl ester transfer protein (CETP)-mediated distribution of neutral lipids that occurs among lipoproteins in plasma, the net mass transfer of core lipids between donor and acceptor lipoproteins in intact plasma was measured in ten healthy normolipidemic subjects. The rate of loss of cholesteryl ester (CE) from high density lipoprotein-3 (HDL3) (19.5 +/- 8.8 nmol/ml per h) was linear and increased significantly (P < 0.01) during the 6-h incubation. Approximately 50% of the CE transferred from HDL3 (118.7 +/- 54.3 nmol/ml) went to very low density lipoprotein (VLDL); the remainder was distributed to low density lipoprotein (LDL) (approximately 30%) and HDL2 (approximately 20%). The rate of loss of triglyceride (TG) from VLDL (14.5 +/- 6.6 nmol/ml per h) to the HDL subfractions and LDL also was linear and increased significantly with time (P < 0.01). About 50% of the TG mass lost from VLDL (85.2 +/- 38.4 nmol/ml) was transferred to LDL and the remainder was recovered in HDL2 (approximately 10%) and HDL3 (approximately 40%). As the number of nmoles of CE lost from HDL3 was almost three times greater than the nmoles of TG it acquired, these findings indicate that the exchange of core lipids in plasma that result from the interaction between CETP-VLDL-HDL3 is not equimolar. Even in the absence of VLDL, HDL3 continued to donate CE to LDL and HDL2 to almost the same degree as in intact plasma (plasma minus VLDL: 17.5 +/- 5.9 nmol/ml per h vs. intact plasma: 20.2 +/- 7.5 nmol/ml per h) without accepting any TG. Our findings demonstrate that independent pathways exist for the transfer of CE and TG among the plasma lipoproteins and, contrary to what is generally believed, a heteroexchange of TG for CE during cholesteryl ester transfer is not obligatory.

HDL biologymechanisms

Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.