Waugh J M, Li-Hawkins J, Yuksel E, Kuo M D, Cifra P N, Hilfiker P R, Geske R, Chawla M, Thomas J, Shenaq S M, Dake M D, Woo S L
Department of Cell Biology, Baylor College of Medicine, Houston, Tex.
Circulation. 2000 Jul 18;102(3):332-7. doi: 10.1161/01.cir.102.3.332.
BACKGROUND-These studies were initiated to confirm that high-level thrombomodulin overexpression is sufficient to limit neointima formation after mechanical overdilation injury. METHODS AND RESULTS-An adenoviral construct expressing thrombomodulin (Adv/RSV-THM) was created and functionally characterized in vitro and in vivo. The impact of local overexpression of thrombomodulin on neointima formation 28 days after mechanical overdilation injury was evaluated. New Zealand White rabbit common femoral arteries were treated with buffer, viral control, or Adv/RSV-THM and subjected to mechanical overdilation injury. The treated vessels (n=4 per treatment) were harvested after 28 days and evaluated to determine intima-to-media (I/M) ratios. Additional experiments were performed to determine early (7-day) changes in extracellular elastin and collagen content; local macrophage, T-cell, and neutrophil infiltration; and local thrombus formation as potential contributors to the observed impact on 28-day neointima formation. The construct significantly decreased neointima formation after mechanical dilation injury in this model. By histological analysis, buffer controls exhibited mean I/M ratios of 0.76+/-0.06%, whereas viral controls reached 0.77+/-0.08%; in contrast, Adv/RSV-THM reduced I/M ratios to 0.47+/-0.06%. Local inflammatory infiltrate decreased in the Adv/RSV-THM group relative to controls, whereas matrix remained relatively preserved. Rates of early thrombus formation also decreased in Adv/RSV-THM animals. CONCLUSIONS-This construct thus offers a viable technique for promoting a locally neointima-resistant small-caliber artery via decreased thrombus bulk, normal matrix preservation, and decreased local inflammation without the inflammatory damage that has limited many other adenoviral applications.
背景——开展这些研究是为了证实高水平血栓调节蛋白过表达足以限制机械性过度扩张损伤后新生内膜的形成。方法与结果——构建了一种表达血栓调节蛋白的腺病毒载体(Adv/RSV-THM),并在体外和体内对其功能特性进行了表征。评估了血栓调节蛋白局部过表达对机械性过度扩张损伤28天后新生内膜形成的影响。用缓冲液、病毒对照或Adv/RSV-THM处理新西兰白兔的股总动脉,并使其遭受机械性过度扩张损伤。28天后收集处理过的血管(每种处理n = 4),并评估其内膜与中膜(I/M)比值。进行了额外的实验以确定细胞外弹性蛋白和胶原蛋白含量的早期(7天)变化;局部巨噬细胞、T细胞和中性粒细胞浸润;以及局部血栓形成,这些可能是观察到的对28天新生内膜形成产生影响的潜在因素。在该模型中,该载体显著减少了机械扩张损伤后的新生内膜形成。通过组织学分析,缓冲液对照组的平均I/M比值为0.76±0.06%,而病毒对照组达到0.77±0.08%;相比之下,Adv/RSV-THM将I/M比值降低至0.47±0.06%。与对照组相比,Adv/RSV-THM组的局部炎症浸润减少,而基质相对保持完好。Adv/RSV-THM处理的动物中早期血栓形成率也降低。结论——因此,该载体提供了一种可行的技术,可通过减少血栓体积、保持正常基质以及减少局部炎症,在不产生限制许多其他腺病毒应用的炎症损伤的情况下,促进局部抗新生内膜的小口径动脉的形成。