Impairment of Macrophage Cholesterol Efflux by Cholesterol Hydroperoxide Trafficking
Author(s) -
Witold Korytowski,
Katarzyna Wawak,
Paweł Pabisz,
Jared C. Schmitt,
Alexandra C. Chadwick,
Daisy Sahoo,
Albert W. Girotti
Publication year - 2015
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.115.306210
Subject(s) - abca1 , downregulation and upregulation , chemistry , gene knockdown , cholesterol , oxidative stress , abcg1 , reverse cholesterol transport , mitochondrion , stimulation , cyp27a1 , biochemistry , microbiology and biotechnology , transporter , endocrinology , biology , lipoprotein , apoptosis , gene
Oxidative stress associated with cardiovascular disease can produce various oxidized lipids, including cholesterol oxides, such as 7-hydroperoxide (7-OOH), 7-hydroxide (7-OH), and 7-ketone (7=O). Unlike 7=O and 7-OH, 7-OOH is redox active, giving rise to the others via potentially toxic-free radical reactions. We tested the novel hypothesis that under oxidative stress conditions, steroidogenic acute regulatory (StAR) family proteins not only deliver cholesterol to/into mitochondria of vascular macrophages, but also 7-OOH, which induces peroxidative damage that impairs early stage reverse cholesterol transport.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom