Transcriptional profiles of valvular and vascular endothelial cells reveal phenotypic differences - Influence of shear stress

被引:143
作者
Butcher, JT
Tressel, S
Johnson, T
Turner, D
Sorescu, G
Jo, H
Nerem, RM
机构
[1] Petit Inst Bioengn & Biosci IBB, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
[3] Georgia Tech, Coulter Dept Biomed Engn, Atlanta, GA USA
[4] Georgia Tech, Div Cardiol, Atlanta, GA USA
[5] Emory Univ, Atlanta, GA 30322 USA
[6] Med Univ S Carolina, Childrens Res Inst, Cardiovasc Dev Biol Ctr, Charleston, SC 29425 USA
关键词
aortic valve; shear stress; inflammation; calcification; endothelial cell;
D O I
10.1161/01.ATV.0000196624.70507.0d
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective - The similarities between valvular and vascular lesions suggest pathological initiation mediated through endothelium, but the role of hemodynamics in valvular endothelial biology is poorly understood. Methods and Results - Monolayers of porcine aortic endothelial cells (PAECs) or porcine aortic valve endothelial cells (PAVECs) were exposed to 20 dyne/cm(2) steady laminar shear stress for 48 hours, with static cultures serving as controls. Multiple microarray comparisons were made using RNA from sheared and control batches of both cell types. More than 400 genes were significantly differentially expressed in each comparison group. The resulting profiles were validated at the transcription and protein level and expression patterns confirmed in vivo by immunohistochemistry. PAVECs were found to be less intrinsically inflammatory than PAECs, but both cell types expressed similar antioxidant and antiinflammatory genes in response to shear stress. PAVECs expressed more genes associated with chondrogenesis, whereas PAECs expressed osteogenic genes, and shear stress had a protective effect against calcification. Conclusions - Transcriptional differences between PAVECs and PAECs highlight the valvular endothelial cell as a distinct organ system and suggest more attention needs to be given to valvular cells to further our understanding of similarities and differences between valvular and vascular pathology.
引用
收藏
页码:69 / 77
页数:9
相关论文
共 36 条
[1]  
*AG TECHN, 2001, AG G2566AA FEAT EXTR
[2]   FORMATION OF CARTILAGE IN BIOPROSTHETIC CARDIAC VALVES IMPLANTED IN SHEEP - A MORPHOLOGIC STUDY [J].
ARBUSTINI, E ;
JONES, M ;
FERRANS, VJ .
AMERICAN JOURNAL OF CARDIOLOGY, 1983, 52 (05) :632-636
[3]   AORTIC-VALVE DISEASE [J].
BAXLEY, WA .
CURRENT OPINION IN CARDIOLOGY, 1994, 9 (02) :152-157
[4]   Unique morphology and focal adhesion development of valvular endothelial cells in static and fluid flow environments [J].
Butcher, JT ;
Penrod, AM ;
García, AJ ;
Nerem, RM .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (08) :1429-1434
[5]   Oscillatory shear stress stimulates adhesion molecule expression in cultured human endothelium [J].
Chappell, DC ;
Varner, SE ;
Nerem, RM ;
Medford, RM ;
Alexander, RW .
CIRCULATION RESEARCH, 1998, 82 (05) :532-539
[6]   DNA microarray analysis of gene expression in endothelial cells in response to 24-h shear stress [J].
Chen, BPC ;
Li, YS ;
Zhao, YH ;
Chen, KD ;
Li, S ;
Lao, JM ;
Yuan, SL ;
Shyy, JYJ ;
Chien, S .
PHYSIOLOGICAL GENOMICS, 2001, 7 (01) :55-63
[7]   Transcriptional profiling and growth kinetics of endothelium reveals differences between cells derived from porcine aorta versus aortic valve [J].
Farivar, RS ;
Cohn, LH ;
Soltesz, EG ;
Mihaljevic, T ;
Rawn, JD ;
Byrne, JG .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2003, 24 (04) :527-534
[8]   Adhesion molecules in nonrheumatic aortic valve disease: Endothelial expression, serum levels and effects of valve replacement [J].
Ghaisas, NK ;
Foley, JB ;
O'Briain, DS ;
Crean, P ;
Kelleher, D ;
Walsh, M .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 36 (07) :2257-2262
[9]   CARTILAGINOUS METAPLASIA IN CALCIFIC AORTIC-VALVE DISEASE [J].
GROOM, DA ;
STARKE, WR .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1990, 93 (06) :809-812
[10]  
HARASAKI H, 1978, J CARDIOVASC SURG, V19, P281