Prothrombotic gene expression profile in vascular smooth muscle cells of human saphenous vein, but not internal mammary artery

被引:24
作者
Payeli, S. K. [1 ,2 ]
Latini, R. [1 ,2 ]
Gebhard, C. [1 ,2 ,4 ]
Patrignani, A. [3 ]
Wagner, U. [3 ]
Luescher, T. F. [1 ,2 ,4 ]
Tanner, F. C. [1 ,2 ,4 ]
机构
[1] Univ Zurich, Inst Physiol, CH-8057 Zurich, Switzerland
[2] Univ Zurich, Ctr Integrat Human Physiol, CH-8057 Zurich, Switzerland
[3] Univ Zurich, Funct Genom Ctr Zurich, CH-8057 Zurich, Switzerland
[4] Univ Zurich Hosp, Ctr Cardiovasc, Zurich, Switzerland
关键词
bypass graft disease; tissue factor; tissue plasminogen activator; coagulation; migration;
D O I
10.1161/ATVBAHA.107.155333
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - The resistance of internal mammary artery (IMA) toward thrombotic occlusion and accelerated atherosclerosis is not well understood. This study analyzed gene expression profiles of vascular smooth muscle cells (VSMCs) from IMA versus saphenous vein (SV). Methods and Results - 54' 675 probe sets were examined by Affymetrix microarrays. Thirty-one genes belonged to the coagulation system; 2 were differentially expressed, namely tissue factor (TF) and tissue-type plasminogen activator (tPA). TF was 3.1-fold lower in IMA than SV (P = 0.006), whereas tPA was 9.0-fold higher (P < 0.001). TF mRNA expression was lower in IMA than SV (P < 0.05); tPA was higher (P < 0.001). TF protein expression was 4.2 +/- 0.5-fold lower in IMA than SV (P < 0.001); tPA was 2.6 +/- 0.4-fold higher (P < 0.01). In IMA VSMC supernatant, TF protein and activity was lower (P < 0.05), TFPI and tPA protein higher (P < 0.05 and P < 0.005), and clotting time of human plasma prolonged (P < 0.05) as compared to SV. Migration to TF/FVIIa (10 (-9) mol/L) was 3-fold lower in IMA than SV (P = 0.01); PAR-2 protein expression was similar (P = NS), PAR-2 blockade without effect (P = NS). Conclusions - Among the genes of the coagulation system, TF and tPA are differentially expressed in VSMCs from IMA versus SV. This is consistent with protection of IMA from thrombus formation and vascular remodeling.
引用
收藏
页码:705 / 710
页数:6
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