Vascular gene expression in atherosclerotic plaque-prone regions analyzed by representational difference analysis

被引:5
作者
Boräng, S
Andersson, T
Thelin, A
Odeberg, J
Lundeberg, J [1 ]
机构
[1] AlbaNova Univ Ctr, KTH, Royal Inst Technol, SCFAB Dept Biotechnol,Div Mol Biotechnol, SE-10691 Stockholm, Sweden
[2] AstraZeneca R&D, Molndal, Sweden
关键词
aorta; atherosclerosis; differential gene expression; endothelium; fluid shear stress; mechanotransduction;
D O I
10.1159/000074426
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objectives: Atherosclerotic plaques are known to develop and progress where the endothelium is subjected to turbulent blood flow. We have applied cDNA representational difference analysis (RDA) to study vascular gene expression in mouse aorta in a model for atherosclerosis. Methods: Gene expression profiles were investigated in plaque-prone and plaque-resistant localizations in the ascending aorta and arch in 8-week-oldApoE-/- and LDLR-/- mice. Total RNA was extracted and two rounds of subtraction were performed; the difference products were characterized in detail by shotgun cloning and analysis of more than 2,700 gene sequences. Results: The identified differentially expressed gene sequences include both genes with known involvement in vascular gene expression and genes previously not implicated in vascular processes. For example, CD36 and caveolin, previously reported for their participation in the progression of atherosclerosis, were found to have an increased expression in vessel localizations thought to be especially susceptible to plaque formation. Conclusions: This report provides new in vivo information of expressed genes that can be useful for further investigations of the molecular mechanisms in focal localization of atherosclerosis. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:107 / 114
页数:8
相关论文
共 27 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]   Monitoring of representational difference analysis subtraction procedures by global microarrays [J].
Andersson, T ;
Unneberg, P ;
Nilsson, P ;
Odeberg, J ;
Quackenbush, J ;
Lundeberg, J .
BIOTECHNIQUES, 2002, 32 (06) :1348-+
[3]   SUBCELLULAR-DISTRIBUTION OF SHEAR-STRESS AT THE SURFACE OF FLOW-ALIGNED AND NONALIGNED ENDOTHELIAL MONOLAYERS [J].
BARBEE, KA ;
MUNDEL, T ;
LAL, R ;
DAVIES, PF .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 268 (04) :H1765-H1772
[4]   Cooperative oligonucleotides in purification of cycle sequencing products [J].
Blomstergren, A ;
O'Meara, D ;
Lukacs, M ;
Uhlén, M ;
Lundeberg, J .
BIOTECHNIQUES, 2000, 29 (02) :352-+
[5]   Monitoring of the subtraction process in solid-phase representational difference analysis:: characterization of a candidate drug [J].
Boräng, S ;
Andersson, T ;
Thelin, A ;
Larsson, M ;
Odeberg, J ;
Lundeberg, J .
GENE, 2001, 271 (02) :183-192
[6]   Exploring the new world of the genome with DNA microarrays [J].
Brown, PO ;
Botstein, D .
NATURE GENETICS, 1999, 21 (Suppl 1) :33-37
[7]   A spatial approach to transcriptional profiling: mechanotransduction and the focal origin of atherosclerosis [J].
Davies, PF ;
Polacek, DC ;
Handen, JS ;
Helmke, BP ;
DePaola, N .
TRENDS IN BIOTECHNOLOGY, 1999, 17 (09) :347-351
[8]   Mechanisms involved in endothelial responses to hemodynamic forces [J].
Davies, PF .
ATHEROSCLEROSIS, 1997, 131 :S15-S17
[9]  
Febbraio M, 2001, J CLIN INVEST, V108, P785, DOI 10.1172/JCI200114006
[10]   IDENTIFYING DIFFERENCES IN MESSENGER-RNA EXPRESSION BY REPRESENTATIONAL DIFFERENCE ANALYSIS OF CDNA [J].
HUBANK, M ;
SCHATZ, DG .
NUCLEIC ACIDS RESEARCH, 1994, 22 (25) :5640-5648