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高频超声与靶向微泡定量检测内皮细胞αvβ3表达:体外与体内研究

Quantification of Endothelial αvβ3 Expression with High-Frequency Ultrasound and Targeted Microbubbles: In Vitro and In Vivo Studies.

作者信息

Daeichin Verya, Kooiman Klazina, Skachkov Ilya, Bosch Johan G, Theelen Thomas L, Steiger Katja, Needles Andrew, Janssen Ben J, Daemen Mat J A P, van der Steen Antonius F W, de Jong Nico, Sluimer Judith C

机构信息

Biomedical Engineering, Thorax Center, Erasmus MC, Rotterdam, The Netherlands.

Biomedical Engineering, Thorax Center, Erasmus MC, Rotterdam, The Netherlands.

出版信息

Ultrasound Med Biol. 2016 Sep;42(9):2283-93. doi: 10.1016/j.ultrasmedbio.2016.05.005. Epub 2016 Jun 11.

Abstract

Angiogenesis is a critical feature of plaque development in atherosclerosis and might play a key role in both the initiation and later rupture of plaques. The precursory molecular or cellular pro-angiogenic events that initiate plaque growth and that ultimately contribute to plaque instability, however, cannot be detected directly with any current diagnostic modality. This study was designed to investigate the feasibility of ultrasound molecular imaging of endothelial αvβ3 expression in vitro and in vivo using αvβ3-targeted ultrasound contrast agents (UCAs). In the in vitro study, αvβ3 expression was confirmed by immunofluorescence in a murine endothelial cell line and detected using the targeted UCA and ultrasound imaging at 18-MHz transmit frequency. In the in vivo study, expression of endothelial αvβ3 integrin in murine carotid artery vessels and microvessels of the salivary gland was quantified using targeted UCA and high-frequency ultrasound in seven animals. Our results indicated that endothelial αvβ3 expression was significantly higher in the carotid arterial wall containing atherosclerotic lesions than in arterial segments without any lesions. We also found that the salivary gland can be used as an internal positive control for successful binding of targeted UCA to αvβ3 integrin. In conclusion, αvβ3-targeted UCA allows non-invasive assessment of the expression levels of αvβ3 on the vascular endothelium and may provide potential insights into early atherosclerotic plaque detection and treatment monitoring.

摘要

血管生成是动脉粥样硬化斑块发展的一个关键特征,可能在斑块的起始和后期破裂中都起关键作用。然而,启动斑块生长并最终导致斑块不稳定的前期分子或细胞促血管生成事件,目前无法通过任何诊断方式直接检测到。本研究旨在探讨使用靶向αvβ3的超声造影剂(UCAs)在体外和体内对内皮αvβ3表达进行超声分子成像的可行性。在体外研究中,通过免疫荧光在小鼠内皮细胞系中证实了αvβ3表达,并使用靶向UCA和18兆赫兹发射频率的超声成像进行检测。在体内研究中,使用靶向UCA和高频超声对7只动物的小鼠颈动脉血管和唾液腺微血管中的内皮αvβ3整合素表达进行了定量。我们的结果表明,含有动脉粥样硬化病变的颈动脉壁中内皮αvβ3表达明显高于无任何病变的动脉节段。我们还发现唾液腺可作为靶向UCA与αvβ3整合素成功结合的内部阳性对照。总之,靶向αvβ3的UCA能够对血管内皮上αvβ3的表达水平进行无创评估,并可能为早期动脉粥样硬化斑块检测和治疗监测提供潜在的见解。

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