Control of cholesteryl ester transfer protein activity by sequestration of lipid transfer inhibitor protein in an inactive complex

• Published in: Journal of lipid research Vol. 49; no. 7; pp. 1529 - 1537
• Main Authors: He, Yubin, Greene, Diane J., Kinter, Michael, Morton, Richard E.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.07.2008; American Society for Biochemistry and Molecular Biology; Elsevier
• Subjects: apolipoprotein A-I; apolipoprotein F; Apolipoproteins - metabolism; Cholesterol Ester Transfer Proteins - metabolism; Cholesterol, LDL - blood; fast-protein liquid chromatography; gel filtration; Humans; hypercholesterolemia; mass spectrometry; Molecular Weight; Protein Binding; fast-protein liquid chromatography; gel filtration; apolipoprotein F; mass spectrometry; apolipoprotein A-I; hypercholesterolemia
• ISSN: 0022-2275; 1539-7262; 1539-7262
• DOI: 10.1194/jlr.M800087-JLR200

Lipid transfer inhibitor protein (LTIP) is a physiologic regulator of cholesteryl ester transfer protein (CETP) function. We previously reported that LTIP activity is localized to LDL, consistent with its greater inhibitory activity on this lipoprotein. With a recently described immunoassay for LTIP, we investigated whether LTIP mass is similarly distributed. Plasma fractionated by gel filtration chromatography revealed two LTIP protein peaks, one coeluting with LDL, and another of ∼470 kDa. The 470 kDa LTIP complex had a density of 1.134 g/ml, indicating ∼50% lipid content, and contained apolipoprotein A-I. By mass spectrometry, partially purified 470 kDa LTIP also contains apolipoproteins C-II, D, E, J, and paraoxonase 1. Unlike LDL-associated LTIP, the 470 kDa LTIP complex does not inhibit CETP activity. In normolipidemic subjects, ∼25% of LTIP is in the LDL-associated, active form. In hypercholesterolemia,this increases to 50%, suggesting that lipoprotein composition may influence the status of LTIP activity. Incubation (37°C) of normolipidemic plasma increased active, LDL-associated LTIP up to 3-fold at the expense of the inactive pool. Paraoxon inhibited this shift by 50%. Overall, these studies show that LTIP activity is controlled by its reversible incorporation into an inactive complex. This may provide for short-term fine-tuning of lipoprotein remodeling mediated by CETP.