Back to Search Start Over

Gene expression differences in healthy brachial and femoral arteries of Rapacz familial hypercholesterolemic swine.

Authors :
Bahls M
Bidwell CA
Hu J
Krueger CG
Reed JD
Tellez A
Kaluza GL
Granada JF
Van Alstine WG
Newcomer SC
Source :
Physiological genomics [Physiol Genomics] 2011 Jun 28; Vol. 43 (12), pp. 781-8. Date of Electronic Publication: 2011 Apr 19.
Publication Year :
2011

Abstract

The mechanisms underlying the unequal distribution of atherosclerotic disease in the peripheral arteries are currently unclear. Gene expression differences in healthy arteries may influence the heterogeneous distribution of atherosclerosis. Therefore, this investigation compares gene expression in healthy atheroprotected brachial and atherosusceptible femoral arteries of young and disease free Rapacz familial hypercholesterolemic (FHC) swine. We hypothesized that transcripts related to atherosusceptibility would be differentially expressed between these arteries prior to the onset of disease. Femoral and brachial arteries were harvested from four 13-day-old Rapacz FHC swine. No atherosclerotic disease was detected using Sudan IV, Verhoeff-van Gieson, and hematoxylin-eosin staining. Gene expression was quantified using Affymetrix GeneChip Porcine Genome Arrays. An average of 15,552 probe sets had detectable transcripts, while 430 probe sets showed a significant differential expression between arteries (false discovery rate < 0.05). The human orthologs of 63 probe sets with differential expression and a 1.5-fold or greater transcript abundance between arteries are associated with Wnt/β-catenin, lysophospholipid, and Ca-signaling, as well as apoptosis. This is the first investigation reporting that differences in relative abundance of gene expression exist between brachial and femoral arteries in young Rapacz FHC swine prior to the development of atherosclerotic lesions.

Details

Language :
English
ISSN :
1531-2267
Volume :
43
Issue :
12
Database :
MEDLINE
Journal :
Physiological genomics
Publication Type :
Academic Journal
Accession number :
21505098
Full Text :
https://doi.org/10.1152/physiolgenomics.00151.2010