| Literature DB >> 23990662 |
Panagiotis Fotakis1, Andreas K Kateifides, Christina Gkolfinopoulou, Dimitra Georgiadou, Melissa Beck, Katharina Gründler, Angeliki Chroni, Efstratios Stratikos, Dimitris Kardassis, Vassilis I Zannis.
Abstract
We investigated the significance of hydrophobic and charged residues 218-226 on the structure and functions of apoA-I and their contribution to the biogenesis of HDL. Adenovirus-mediated gene transfer of apoA-I[L218A/L219A/V221A/L222A] in apoA-I⁻/⁻ mice decreased plasma cholesterol and apoA-I levels to 15% of wild-type (WT) control mice and generated pre-β- and α4-HDL particles. In apoA-I⁻/⁻ × apoE⁻/⁻ mice, the same mutant formed few discoidal and pre-β-HDL particles that could not be converted to mature α-HDL particles by excess LCAT. Expression of the apoA-I[E223A/K226A] mutant in apoA-I⁻/⁻ mice caused lesser but discrete alterations in the HDL phenotype. The apoA-I[218-222] and apoA-I[E223A/K226A] mutants had 20% and normal capacity, respectively, to promote ABCA1-mediated cholesterol efflux. Both mutants had ∼65% of normal capacity to activate LCAT in vitro. Biophysical analyses suggested that both mutants affected in a distinct manner the structural integrity and plasticity of apoA-I that is necessary for normal functions. We conclude that the alteration of the hydrophobic 218-222 residues of apoA-I disrupts apoA-I/ABCA1 interactions and promotes the generation of defective pre-β particles that fail to mature into α-HDL subpopulations, thus resulting in low plasma apoA-I and HDL. Alterations of the charged 223, 226 residues caused milder but discrete changes in HDL phenotype.Entities:
Keywords: LCAT; apolipoprotein A-I mutations; dyslipidemia; pre-β and α-HDL particles
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Year: 2013 PMID: 23990662 PMCID: PMC3826676 DOI: 10.1194/jlr.M038356
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922