Rix Anne, Fokong Stanley, Heringer Sarah, Pjontek Rastislav, Kabelitz Lisa, Theek Benjamin, Brockmann Marc-Alexander, Wiesmann Martin, Kiessling Fabian
From the *Institute for Experimental Molecular Imaging, University Clinic and Helmholtz Center for Biomedical Engineering, and †Department of Diagnostic and Interventional Neuroradiology, RWTH Aachen University, Aachen, Germany.
Invest Radiol. 2016 Dec;51(12):767-775. doi: 10.1097/RLI.0000000000000282.
Interventions such as balloon angioplasty can cause vascular injury leading to platelet activation, thrombus formation, and inflammatory response. This induces vascular smooth muscle cell activation and subsequent re-endothelialization with expression of αvβ3-integrin by endothelial cells and vascular smooth muscle cell. Thus, poly-N-butylcyanoacrylate microbubbles (MBs) targeted to αvβ3-integrin were evaluated for monitoring vascular healing after vessel injury in pigs using molecular ultrasound imaging.
Approval for animal experiments was obtained. The binding specificity of αvβ3-integrin-targeted MB to human umbilical vein endothelial cells was tested with fluorescence microscopy. In vivo imaging was performed using a clinical ultrasound system and an 8-MHz probe. Six mini pigs were examined after vessel injury in the left carotid artery. The right carotid served as control. Uncoated MB, cDRG-coated MB, and αvβ3-integrin-specific cRGD-coated MB were injected sequentially. Bound MBs were assessed 8 minutes after injection using ultrasound replenishment analysis. Measurements were performed 2 hours, 1 and 5 weeks, and 3 and 6 months after injury. In vivo data were validated by immunohistochemistry.
Significantly stronger binding of cRGD-MB than MB and cDRG-MB to human umbilical vein endothelial cells was found (P < 0.01). As vessel injury leads to upregulation of αvβ3-integrin, cRGD-MBs bound significantly stronger (P < 0.05) in injured carotid arteries than at the counter side 1 week after vessel injury and significant differences could also be observed after 5 weeks. After 3 months, αvβ3-integrin expression decreased to baseline and binding of cRGD-MB was comparable in both vessels. Values remained at baseline also after 6 months.
Ultrasound imaging with RGD-MB is promising for monitoring vascular healing after vessel injury. This may open new perspectives to assess vascular damage after radiological interventions.
诸如球囊血管成形术等干预措施可导致血管损伤,进而引发血小板活化、血栓形成及炎症反应。这会诱导血管平滑肌细胞活化,并随后通过内皮细胞和血管平滑肌细胞表达αvβ3整合素实现再内皮化。因此,使用分子超声成像技术,对靶向αvβ3整合素的聚N - 丁基氰基丙烯酸酯微泡(MBs)进行评估,以监测猪血管损伤后的血管愈合情况。
获得动物实验批准。用荧光显微镜检测靶向αvβ3整合素的MB与人脐静脉内皮细胞的结合特异性。使用临床超声系统和8兆赫探头进行体内成像。对6只小型猪的左颈动脉进行血管损伤后检查。右侧颈动脉作为对照。依次注射未包被的MB、cDRG包被的MB和αvβ3整合素特异性cRGD包被的MB。注射后8分钟使用超声补充分析评估结合的MBs。在损伤后2小时、1周和5周以及3个月和6个月进行测量。体内数据通过免疫组织化学验证。
发现cRGD - MB与人脐静脉内皮细胞的结合明显强于MB和cDRG - MB(P < 0.01)。由于血管损伤导致αvβ3整合素上调,在血管损伤后1周,cRGD - MB在受伤的颈动脉中的结合明显更强(P < 0.05),5周后也可观察到显著差异。3个月后,αvβ3整合素表达降至基线,cRGD - MB在两条血管中的结合相当。6个月后数值也保持在基线水平。
使用RGD - MB进行超声成像有望监测血管损伤后的血管愈合情况。这可能为评估放射学干预后的血管损伤开辟新的前景。