Wang Xin, Zhao Rong, Liu Changjian, Qiao Tong
Department of Vascular Surgery, Affiliated Drum Tower Hospital, Medical College of Nanjing University.
Phlebology. 2013 Mar;28(2):93-100. doi: 10.1258/phleb.2012.012018. Epub 2013 May 6.
To investigate the abnormal expressions of Tie1 on the valves of great saphenous varicose vein, and to discuss the relationship between the phenomenon and pathogenesis of varicose vein of lower extremity.
Varicose veins group 18 samples, normal control group 14 samples. Immunohistochemistry staining has investigated the expression of CD31 and Tie1 in the first valves of great saphenous veins. Semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) has checked mRNA expression of Tie1. Western blot has checked the expression of Tie1 protein in venous valves.
In normal control group valves, there was no difference between proximal and distal sides endothelium, which expressing CD31 in both valvar basement and valve cusp (positive endothelial cells [ECs] percentage: P > 0.05, P > 0.05). However, the endothelium of the proximal side demonstrates Tie1 stronger than distal side in valvar basement (positive ECs percentage: P < 0.05), which was not found at valve cusp (positive ECs percentage: P > 0.05). In varicose veins group, the endothelium of proximal side cells expresses CD31 weaker than distal side at both valvar basement and valve cusp (positive ECs percentage: P < 0.05, P < 0.05) besides the morphological alteration of valves. Moreover, it expresses Tie1 much weaker than diatal side (positive ECs percentage: P < 0.01). Semi-quantitative RT-PCR showed that valves of varicose veins group expressed Tie1 much weaker than the normal control group (P < 0.01). Western blot could not detect the expression of Tie1 in venous valves.
The decreasing expression of Tie1 may play an important role in the pathogenesis of primary lower extremity varicose veins.
研究Tie1在大隐静脉曲张瓣膜中的异常表达情况,并探讨该现象与下肢静脉曲张发病机制之间的关系。
静脉曲张组18例样本,正常对照组14例样本。采用免疫组织化学染色法检测大隐静脉第一瓣膜中CD31和Tie1的表达。运用半定量逆转录-聚合酶链反应(RT-PCR)检测Tie1的mRNA表达。通过蛋白质免疫印迹法检测静脉瓣膜中Tie1蛋白的表达。
在正常对照组瓣膜中,瓣膜基底和瓣尖处近端和远端内皮细胞CD31表达无差异(阳性内皮细胞[ECs]百分比:P>0.05,P>0.05)。然而,在瓣膜基底处近端内皮细胞Tie1表达强于远端(阳性ECs百分比:P<0.05),在瓣尖处未发现此差异(阳性ECs百分比:P>0.05)。在静脉曲张组中,除瓣膜形态改变外,瓣膜基底和瓣尖处近端细胞CD31表达均弱于远端(阳性ECs百分比:P<0.05,P<0.05)。此外,近端细胞Tie1表达远弱于远端(阳性ECs百分比:P<0.01)。半定量RT-PCR显示,静脉曲张组瓣膜Tie1表达明显弱于正常对照组(P<0.01)。蛋白质免疫印迹法未检测到静脉瓣膜中有Tie1表达。
Tie1表达降低可能在原发性下肢静脉曲张发病机制中起重要作用。