A CYP26B1 polymorphism enhances retinoic acid catabolism and may aggravate atherosclerosisShow others and affiliations
2012 (English)In: Molecular Medicine, ISSN 1076-1551, E-ISSN 1528-3658, Vol. 18, no 1, p. 712-718
Article in journal (Refereed) Published
Abstract [en]
All-trans retinoic acid, controlled by CYP26 enzymes, potentially has beneficial effects in atherosclerosis treatment. This study investigates CYP26B1 in atherosclerosis and effects of a genetic polymorphism in CYP26B1 on retinoid catabolism. We found that CYP26B1 mRNA was induced by retinoic acid in human atherosclerotic arteries and CYP26B1 and the macrophage marker CD68 co-localized in human atherosclerotic lesions. In mice, Cyp26B1 mRNA was higher in atherosclerotic than normal arteries. Databases were queried for non-synonymous CYP26B1 SNPs and rs2241057 selected for further studies. Constructs of the CYP26B1 variants were created and used for production of purified proteins and transfection of macrophage-like cells. The minor variant catabolized retinoic acid with significantly higher efficiency, indicating that rs2241057 is functional and suggesting reduced retinoid availability in tissues with the minor variant. rs2241057 was investigated in a Stockholm Coronary Atherosclerosis Risk Factor (SCARF) subgroup. The minor allele was associated with slightly larger lesions as determined by angiography. In summary, this study identifies the first CYP26B1 polymorphism that alters CYP26B1 capacity to metabolize retinoic acid. CYP26B1 was expressed in macrophage-rich areas of human atherosclerotic lesions, induced by retinoic acid and increased in murine atherosclerosis. Taken together, the results indicate that CYP26B1 capacity is genetically regulated and suggest that local CYP26B1 activity may influence atherosclerosis.
Place, publisher, year, edition, pages
New York, USA: The Feinstein Institute for Medical Research , 2012. Vol. 18, no 1, p. 712-718
National Category
Medical and Health Sciences Biochemistry Molecular Biology
Research subject
Medicine
Identifiers
URN: urn:nbn:se:oru:diva-23259DOI: 10.2119/molmed.2012.00094ISI: 000306034400018PubMedID: 22415012Scopus ID: 2-s2.0-84887594213OAI: oai:DiVA.org:oru-23259DiVA, id: diva2:530992
Funder
Swedish Heart Lung FoundationSwedish Society for Medical Research (SSMF)Wenner-Gren Foundations
Note
Funding Agencies:
Swedish Health Care Sciences Postgraduate School (NFVO) at Karolinska Institutet
Bergwall's Foundation
2012-06-052012-06-052025-02-20Bibliographically approved
In thesis