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HDL biology

HDL triglyceride and free cholesterol content noncompetitively inhibit CETP, while HDL apoprotein composition uncompetitively modulates it (J Lipid Res 1989)

Original title: Transfer of cholesteryl ester into high density lipoprotein by cholesteryl ester transfer protein: effect of HDL lipid and apoprotein content

J Lipid Res · · 7

Sparks DL, Pritchard PH

Recombinant HDL (rHDL) particles of defined lipid and apoprotein composition were incubated with partially purified CETP and radiolabeled LDL to study how HDL composition affects CETP-mediated cholesteryl ester transfer. Increasing rHDL triglyceride content relative to cholesteryl ester significantly reduced the particles' ability to accept CETP-transferred cholesteryl esters, with kinetic analysis showing a significant reduction in maximum transfer velocity (Tmax) but little change in the HDL concentration for half-maximal velocity (KH); increasing free cholesterol relative to phospholipid produced a similar reduction. In contrast, rHDL made from purified apoA-I, apoA-II, or both had significantly elevated Tmax and KH values. The authors conclude that rHDL triglyceride or free cholesterol content noncompetitively inhibits CETP catalytic activity, while an as-yet-unidentified HDL apoprotein component beyond apoA-I or apoA-II uncompetitively inhibits CETP by altering both Tmax and KH.

PubMed

Original abstract

Recombinant high density lipoprotein (rHDL) particles were prepared by cosonication of purified lipids and human apoproteins and incubated with partly purified cholesteryl ester transfer protein (CETP) and low density lipoprotein (LDL) containing [3H]cholesteryl ester. Increasing the triglyceride content relative to cholesteryl ester in rHDL significantly decreased the ability of the particles to accept cholesteryl esters transferred by CETP. Kinetic analysis of the data was performed to numerically define the maximum velocity of lipid transfer, Tmax, and the HDL concentration required for half maximal velocity, KH. Increases in rHDL-triglyceride content were shown to result in a significant reduction in the Tmax without a major change in KH. When the free cholesterol content was increased relative to phospholipid, the ability of the particles to accept cholesteryl esters was also decreased in a similar manner. Conversely, rHDL prepared from purified apoprotein A-I, A-II, or mixtures of both, had significantly elevated Tmax and KH values for their interaction with CETP. The results suggest that increases in triglyceride or free cholesterol content of an rHDL particle decrease the catalytic ability of CETP by noncompetitive inhibition. In addition, some component(s) of HDL apoproteins, other than A-I or A-II, were shown to uncompetitively inhibit the activity of CETP, by modifying both Tmax and the KH for the reaction. This study has shown that altered HDL composition may have marked effects on the transfer and equilibration of cholesteryl esters within the HDL pool.

HDL biologymechanisms

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