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HDL biology

CETP and hepatic lipase together shed apoA-I from HDL, which reassembles into new discoidal particles (Biochim Biophys Acta 1992)

Original title: Cholesteryl ester transfer protein and hepatic lipase activity promote shedding of apo A-I from HDL and subsequent formation of discoidal HDL

Biochim Biophys Acta · · 7

Clay MA, Newnham HH, Forte TM, Barter PI

Human plasma supplemented with additional VLDL, CETP, and hepatic lipase was incubated at 37 degrees C for up to 8 hours to study the effects of lipid transfers and hepatic lipase on HDL concentration, composition, particle size, and morphology. HDL became depleted of cholesteryl esters and reduced in particle size, and within 2 hours had lost about 30% of its apoA-I. With extended incubation beyond 2 hours, apoA-I returned progressively to the HDL fraction until, by 8 hours, its concentration matched that of non-incubated samples, accompanied by the progressive appearance of discoidal HDL particles on electron microscopy. The authors conclude that CETP- and hepatic lipase-driven depletion of HDL core lipid and particle size is accompanied by shedding of apoA-I, which then nucleates new discoidal HDL particles, a process of considerable potential physiological importance.

Read the paper (DOI)PubMed

Original abstract

The effects of lipid transfers and hepatic lipase (HL) on the concentration, composition, particle size distribution and morphology of high density lipoproteins (HDL) have been investigated. Human plasma supplemented with additional very low density lipoproteins (VLDL), cholesteryl ester transfer protein (CETP) and HL has been incubated at 37 degrees C for up to 8 h. The HDL became depleted of cholesteryl esters and reduced in particle size. Within 2 h of such incubation they had also lost about 30% of their apo A-I. However, with extension of the incubations beyond 2 h, the apo A-I returned progressively to the HDL fraction until, after 8 h, the concentration of apo A-I in HDL was identical to that in non-incubated samples. This return of apo A-I to the HDL density range was accompanied by a progressive appearance in electron micrographs of discoidal HDL particles. Thus, the depletion of the core lipid content and the reduction in particle size of HDL promoted by lipid transfers and HL activity in vitro is accompanied by a shedding of apo A-I which forms the nucleus of new discoidal HDL particles. The potential physiological importance of such a process is considerable.

HDL biologymechanisms

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