4.6 Article

Analysis of lipid transfer activity between model nascent HDL particles and plasma lipoproteins: implications for current concepts of nascent HDL maturation and genesis

期刊

JOURNAL OF LIPID RESEARCH
卷 51, 期 4, 页码 785-797

出版社

ELSEVIER
DOI: 10.1194/jlr.M001875

关键词

nascent apoA-I-containing particle; remodeling of high density lipoprotein; origin of high density lipoprotein; ATP binding cassette transporter A1; lecithin:cholesterol acyltransferase; phospholipid transfer protein

资金

  1. Canadian Institutes of Health Research [MOP 15042]
  2. Heart and Stroke Foundation of Canada

向作者/读者索取更多资源

The specifics of nascent HDL remodeling within the plasma compartment remain poorly understood. We developed an in vitro assay to monitor the lipid transfer between model nascent HDL (LpA-I) and plasma lipoproteins. Incubation of alpha-I-125-LpA-I with plasma resulted in association of LpA-I with existing plasma HDL, whereas incubation with TD plasma or LDL resulted in conversion of alpha-I-125-LpA-I to pre beta-HDL. To further investigate the dynamics of lipid transfer, nascent LpA-I were labeled with cell-derived [H-3] cholesterol (UC) or [H-3] phosphatidylcholine (PC) and incubated with plasma at 37 degrees C. The majority of UC and PC were rapidly transferred to apolipoprotein B (apoB). Subsequently, UC was redistributed to HDL for esterification before being returned to apoB. The presence of a phospholipid transfer protein (PLTP) stimulator or purified PLTP promoted PC transfer to apoB. Conversely, PC transfer was abolished in plasma from PLTP-/- mice. Injection of I-125-LpA-I into rabbits resulted in a rapid size redistribution of I-125-LpA-I. The majority of [H-3] UC from labeled r(HDL) was esterified in vivo within HDL, whereas a minority was found in LDL. These data suggest that apoB plays a major role in nascent HDL remodeling by accepting their lipids and donating UC to the LCAT reaction. The finding that nascent particles were depleted of their lipids and remodeled in the presence of plasma lipoproteins raises questions about their stability and subsequent interaction with LCAT.-Bailey, D., I. Ruel, A. Hafiane, H. Cochrane, I. Iatan, M. Jauhiainen, C. Ehnholm, L. Krimbou, and J. Genest. Analysis of lipid transfer activity between model nascent HDL particles and plasma lipoproteins: implications for current concepts of nascent HDL maturation and genesis. J. Lipid Res. 2010. 51: 785-797.

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