Specific Targeting of Human Inflamed Endothelium and In Situ Vascular Tissue Transfection by the Use of Ultrasound Contrast Agents

被引:23
作者
Barreiro, Olga [1 ,2 ]
Aguilar, Rio J. [3 ]
Tejera, Emilio [1 ,2 ]
Megias, Diego [4 ]
de Torres-Alba, Fernando [3 ]
Evangelista, Arturo [3 ]
Sanchez-Madrid, Francisco [1 ,2 ]
机构
[1] Univ Autonoma Madrid, Hosp Princesa, Serv Inmunol, Madrid 28006, Spain
[2] Ctr Nacl Invest Cardiovasc, Dept Biol Vasc & Inflamac, Madrid, Spain
[3] Hosp Valle De Hebron, Serv Cardiol, Barcelona, Spain
[4] Ctr Nacl Invest Oncol, Unidad Microscopia, Madrid, Spain
基金
瑞典研究理事会;
关键词
ultrasound; microbubbles; human umbilical cord; targeting; inflammation; sonoporation; INTERCELLULAR-ADHESION MOLECULE-1; ADHERENT LEUKOCYTES; MICROBUBBLES; DELIVERY; MICRODOMAINS; INFLAMMATION; EXPRESSION; INJURY; CELLS;
D O I
10.1016/j.jcmg.2009.04.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES We used human umbilical cord segments as an ex vivo model to investigate the possible clinical diagnostic and therapeutic applications of microbubbles (MBs). BACKGROUND Microbubbles are commonly used in clinical practice as ultrasound contrast agents. Several studies have addressed the in vivo applications of MBs for specific targeting of vascular dysfunction or sonoporation in animal models, but to date no human tissue model has been established. METHODS Primary venular endothelial cell monolayers were targeted with MBs conjugated to an antibody against a highly expressed endothelial marker (tetraspanin CD9), and binding was assessed under increasing flow rates (0.5 to 5 dynes/cm(2)). Furthermore, CD9-coupled MB endothelial targeting was measured under flow conditions by contrast-enhanced ultrasound analysis in an ex vivo human macrovascular model (umbilical cord vein), and the same tissue model was used for the detection of inflamed vasculature with anti-intercellular adhesion molecule (ICAM)-1-coated MBs. Finally, plasmids encoding fluorescent proteins were sonoporated into umbilical cord vessels. RESULTS Specific endothelial targeting in the in vitro and ex vivo models described previously was achieved by the use of MBs covered with an anti-CD9. Furthermore, we managed to induce inflammation in umbilical cord veins and detect it with real-time echography imaging using anti-ICAM-1-coupled MBs. Moreover, expression and correct localization of green fluorescent protein and green fluorescent protein-tagged ICAM-1 were assessed in this human ex vivo model without causing vascular damage. CONCLUSIONS In the absence of clinical trials to test the benefits and possible applications of ultrasound contrast agents for molecular imaging and therapy, we have developed a novel ex vivo human model using umbilical cords that is valid for the detection of inflammation and for exogenous expression of proteins by sonoporation. (J Am Coll Cardiol Img 2009;2:997-1005) (C) 2009 by the American College of Cardiology Foundation
引用
收藏
页码:997 / 1005
页数:9
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