Gene expression differences during the heterogeneous progression of peripheral atherosclerosis in familial hypercholesterolemic swine

被引:9
作者
Bahls, Martin [1 ,2 ]
Bidwell, Christopher A. [3 ]
Hu, Juan [4 ]
Tellez, Armando [5 ]
Kaluza, Greg L. [5 ]
Granada, Juan F. [5 ]
Krueger, Christian G. [6 ]
Reed, Jess D. [6 ]
Laughlin, M. Harold [7 ]
Van Alstine, William G. [8 ]
Newcomer, Sean C. [1 ,9 ]
机构
[1] Purdue Univ, Dept Hlth & Kinesiol, W Lafayette, IN 47907 USA
[2] Univ Med Greifswald, Klin & Poliklin Innere Med B, Greifswald, Germany
[3] Purdue Univ, Dept Anim Sci, W Lafayette, IN 47907 USA
[4] Purdue Univ, Dept Stat, W Lafayette, IN 47907 USA
[5] Cardiovasc Res Fdn, Skirball Ctr Cardiovasc Res, New York, NY USA
[6] Univ Wisconsin, Dept Anim Sci, Madison, WI USA
[7] Univ Missouri, Dept Biomed Sci, Columbia, MO USA
[8] Purdue Univ, Dept Vet Pathobiol, W Lafayette, IN 47907 USA
[9] Calif State Univ San Marcos, San Marcos, CA USA
关键词
Peripheral arterial disease; Atherosclerosis; Vascular biology; Peripheral vasculature; Gene expression; ENDOTHELIAL TRANSCRIPTIONAL PROFILES; FEMORAL ARTERIES; ILIAC ARTERIES; LESIONS; CORONARY; DISEASE; SUSCEPTIBILITY; MICROARRAY; PIGS;
D O I
10.1186/1471-2164-14-443
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The heterogeneous progression of atherosclerotic disease in the peripheral arteries is currently not well understood. In humans, artery specific disease progression is partly attributed to the local hemodynamic environments. However, despite similar hemodynamic environments, porcine brachial arteries are protected while femoral arteries are highly susceptible to advanced lesion formation. The aim of this investigation was to determine whether artery specific gene expression patterns contribute to the uneven distribution of peripheral arterial disease (PAD) in Rapacz Familial-Hypercholesterolemic (FHC) swine. Results: Histological results confirmed rapid atherosclerotic disease progression in femoral but not brachial arteries. A total of 18,922 probe sets had sufficient signal abundance. A main effect for age and artery was observed for 1784 and 1256 probe sets, respectively. A significant age x artery interaction was found for 184 probe sets. Furthermore, comparison between arteries found a decrease from 714 to 370 differentially expressed transcripts from nine months to two years of age. Gene ontology analysis of the 56 genes with a main effect for artery and an age x artery interaction identified vascular smooth muscle contraction as enhanced biological signaling pathway. Conclusion: This is the first investigation to report that the total number of differential genes decreases with diverging atherosclerotic disease pattern between porcine brachial and femoral arteries.
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页数:16
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