Open AccessQuantitative and qualitative methods using fluorescence microscopy for the study of modified low density lipoproteins uptake
Author(s) -
Leyva Francisco J.,
Pershouse Mark A.
Publication year - 2009
Publication title -
scanning
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.359
H-Index - 47
eISSN - 1932-8745
pISSN - 0161-0457
DOI - 10.1002/sca.20155
Subject(s) - fluorescence microscope , scavenger receptor , fluorescence , lipoprotein , chemistry , microbiology and biotechnology , low density lipoprotein , biophysics , cell , biochemistry , biology , cholesterol , physics , quantum mechanics
Atherosclerosis and heart disease are the main cause of death in United States. The development of atherosclerosis includes lipid deposition and foam cell formation in the artery wall. Scavenger Receptors A‐I and II (SRA‐I/II) have an important role of in foam cell formation and atherogenesis. Most of the SRA‐I/II studies had been performed using Iodine‐125‐radiolabeled modified low‐density lipoprotein. This report attempts to validate the use of fluorescence microscopy techniques as an alternative to obtain qualitative and quantitative information of the uptake of fluorescence‐labeled acetylated low‐density lipoprotein (AcLDL) in adherent CHO cells expressing SRA‐I/II. After verifying the protein expression of SRA‐I and II, uptake was quantified using a Laser Scan Cytometer, and images of cells containing fluorescent AcLDL were obtained. A significant increase in fluorescence was found in the cells transfected with SRA‐I/II vs. those with empty vector. When SRA‐I/II competitive ligands were used, the uptake of AcLDL was significantly decreased. In conclusion, the use of fluorescence microscopy techniques in obtaining qualitative and quantitative information of the uptake of fluorescence‐labeled AcLDL by adherent cells, such as CHO cells, is an alternative to the traditional use of radiolabeled iodine. SCANNING 31: 167–173, 2009. © 2009 Wiley Periodicals, Inc.