Direct observation of cargo transfer from HDL particles to the plasma membrane

Atherosclerosis. 2018 Oct:277:53-59. doi: 10.1016/j.atherosclerosis.2018.08.032. Epub 2018 Aug 27.

Abstract

Background and aims: Exchange of cholesterol between high-density lipoprotein (HDL) particles and cells is a key process for maintaining cellular cholesterol homeostasis. Recently, we have shown that amphiphilic cargo derived from HDL can be transferred directly to lipid bilayers. Here we pursued this work using a fluorescence-based method to directly follow cargo transfer from HDL particles to the cell membrane.

Methods: HDL was either immobilized on surfaces or added directly to cells, while transfer of fluorescent cargo was visualized via fluorescence imaging.

Results: In Chinese hamster ovary (CHO) cells expressing the scavenger receptor class B type 1 (SR-B1), transfer of amphiphilic cargo from HDL particles to the plasma membrane was observed immediately after contact, whereas hydrophobic cargo remained associated with the particles; about 60% of the amphiphilic cargo of surface-bound HDL was transferred to the plasma membrane. Essentially no cargo transfer was observed in cells with low endogenous SR-B1 expression. Interestingly, transfer of fluorescently-labeled cholesterol was also facilitated by using an artificial linker to bind HDL to the cell surface.

Conclusions: Our data hence indicate that the tethering function of SR-B1 is sufficient for efficient transfer of free cholesterol to the plasma membrane.

Keywords: Cholesterol; HDL; Single molecule microscopy; transfer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD36 Antigens / metabolism*
  • CHO Cells
  • Cell Membrane / metabolism*
  • Cholesterol, HDL / blood*
  • Cricetulus
  • Hep G2 Cells
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Hydrophobic and Hydrophilic Interactions
  • Microscopy, Fluorescence*
  • Protein Transport
  • Single Molecule Imaging / methods*
  • Surface Properties
  • Time Factors

Substances

  • CD36 Antigens
  • Cholesterol, HDL