High glucose, unsaturated and saturated fatty acids differentially regulate expression of ATP-binding cassette transporters ABCA1 and ABCG1 in human macrophages.

Abstract

The ATP-binding cassette transporters ABCA1 and ABCG1 are highly expressed in macrophage-derived foam cells and promote reverse cholesterol efflux via biogenesis of high-density lipoproteins. The aim of this study was to analyze the direct effects of bioactive factors related to the metabolic syndrome on macrophage transcript levels of all 47 human ABC transporters. Using in vitro M-CSF predifferentiated macrophages and TaqMan low density arrays we could show that linoleic acid, palmitic acid, and high glucose levels have a major impact on ABCA1 and ABCG1 expression but do not strongly affect most other human ABC transporters. In Western blot experiments we demonstrate that ABCA1 and ABCG1 protein levels are synchronously suppressed by high glucose levels and the w6-unsaturated fatty acid linoleic acid. We conclude that metabolites associated with the metabolic syndrome enhance the formation of atherosclerotic lesions by diminishing the reverse cholesterol transport function of ABCA1 and ABCG1.

• Authors: Richard Mauerer, Stefanie Ebert, Thomas Langmann
• Journal: Experimental & molecular medicine (Exp Mol Med) Vol. 41 Issue 2 Pg. 126-32 (Feb 28 2009) ISSN: 1226-3613 [Print] United States
• PMID: 19287193 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• ABCA1 protein, human
• ABCG1 protein, human
• ATP Binding Cassette Transporter 1
• ATP Binding Cassette Transporter, Subfamily G, Member 1
• ATP-Binding Cassette Transporters
• Fatty Acids
• Fatty Acids, Unsaturated
• RNA, Messenger
• Glucose

Topics

• ATP Binding Cassette Transporter 1
• ATP Binding Cassette Transporter, Subfamily G, Member 1
• ATP-Binding Cassette Transporters (genetics)
• Cells, Cultured
• Fatty Acids (genetics, metabolism)
• Fatty Acids, Unsaturated (genetics, metabolism)
• Gene Expression Profiling
• Gene Expression Regulation
• Glucose (genetics, metabolism)
• Humans
• Macrophages (metabolism)
• RNA, Messenger (metabolism)
• Time Factors