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
Original language | English |
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Pages (from-to) | 53-59 |
Number of pages | 7 |
Journal | Atherosclerosis |
Volume | 277 |
DOIs | |
Publication status | Published - Oct 2018 |
Keywords
- Cholesterol
- HDL
- Single molecule microscopy
- transfer
- Human Umbilical Vein Endothelial Cells
- Cricetulus
- Humans
- Hep G2 Cells
- Protein Transport
- Animals
- Cholesterol, HDL/blood
- Time Factors
- Cell Membrane/metabolism
- Surface Properties
- Hydrophobic and Hydrophilic Interactions
- Single Molecule Imaging/methods
- CD36 Antigens/metabolism
- Microscopy, Fluorescence
- CHO Cells