4.6 Article

Micellar lipid composition affects micelle interaction with class B scavenger receptor extracellular loops

Journal

JOURNAL OF LIPID RESEARCH
Volume 56, Issue 6, Pages 1123-1133

Publisher

ELSEVIER
DOI: 10.1194/jlr.M057612

Keywords

scavenger receptor class B type I; cluster determinant 36; cholesterol; phospholipids; fatty acid; cholecalciferol; intestine; surface plasmon resonance

Funding

  1. CIFRE (Conventions Industrielles de Formation par la REcherche) from the ANRT (French national association for research and technology)
  2. Lesieur Inc.

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Scavenger receptors (SRs) like cluster determinant 36 (CD36) and SR class B type I (SR-BI) play a debated role in lipid transport across the intestinal brush border membrane. We used surface plasmon resonance to analyze real-time interactions between the extracellular protein loops and various ligands ranging from single lipid molecules to mixed micelles. Micelles mimicking physiological structures were necessary for optimal binding to both the extracellular loop of CD36 (lCD36) and the extracellular loop of SR-BI (lSR-BI). Cholesterol, phospholipid, and fatty acid micellar content significantly modulated micelle binding to and dissociation from the transporters. In particular, high phospholipid micellar concentrations inhibited micelle binding to both receptors (-53.8 and -74.4% binding at 0.32 mM compared with 0.04 mM for lCD36 and lSR-BI, respectively, P < 0.05). The presence of fatty acids was crucial for micelle interactions with both proteins (94.4 and 81.3% binding with oleic acid for lCD36 and lSR-BI, respectively, P < 0.05) and fatty acid type substitution within the micelles was the component that most impacted micelle binding to the transporters. These effects were partly due to subsequent modifications in micellar size and surface electric charge, and could be correlated to micellar vitamin D uptake by Caco-2 cells. Our findings show for the first time that micellar lipid composition and micellar properties are key factors governing micelle interactions with SRs.

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