Abstract |
We have cloned a human macrophage receptor that binds to apolipoprotein (apo)B48 of dietary triglyceride (TG)-rich lipoproteins. TG-rich lipoprotein uptake by the apoB48R rapidly converts macrophages and apoB48R-transfected Chinese hamster ovary cells in vitro into lipid-filled foam cells, as seen in atherosclerotic lesions. The apoB48R cDNA (3,744 bp) encodes a protein with no known homologs. Its approximately 3.8-kb mRNA is expressed primarily by reticuloendothelial cells: monocytes, macrophages, and endothelial cells. Immunohistochemistry shows the apoB48R is in human atherosclerotic lesion foam cells. Normally, the apoB48R may provide essential lipids to reticuloendothelial cells. If overwhelmed, foam cell formation, endothelial dysfunction, and atherothrombogenesis may ensue, a mechanism for cardiovascular disease risk of elevated TG.
|
Authors | M L Brown, M P Ramprasad, P K Umeda, A Tanaka, Y Kobayashi, T Watanabe, H Shimoyamada, W L Kuo, R Li, R Song, W A Bradley, S H Gianturco |
Journal | Proceedings of the National Academy of Sciences of the United States of America
(Proc Natl Acad Sci U S A)
Vol. 97
Issue 13
Pg. 7488-93
(Jun 20 2000)
ISSN: 0027-8424 [Print] United States |
PMID | 10852956
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
|
Chemical References |
- Apolipoprotein B-48
- Apolipoproteins B
- DNA, Complementary
- Receptors, Lipoprotein
- Triglycerides
- apo B48 receptor
|
Topics |
- Amino Acid Sequence
- Animals
- Apolipoprotein B-48
- Apolipoproteins B
(physiology)
- Arteriosclerosis
- CHO Cells
- Cloning, Molecular
- Cricetinae
- DNA, Complementary
(genetics, isolation & purification)
- Humans
- Macrophages
(physiology)
- Molecular Sequence Data
- Receptors, Lipoprotein
(genetics, metabolism)
- Triglycerides
(metabolism)
|