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携Sialyl Lewis^X与携抗P-选择素单抗靶向超声微泡粘附性的对比研究 被引量:5

Assessment of targeted adhesion of the two ultrasound contrast agents:one with Sialyl Lewis^X and the other with anti-P-selectin monoclone antibody in vitro
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摘要 目的对比评价携sialylLewis。与携抗P-选择素单抗靶向超声微泡粘附特性。方法采用“亲和素-生物素”桥接法构建携Sialyl Lewis、(MB-S)、携抗P-选择素单抗靶向超声微泡(MB-P)及携同型抗体微泡(MB-C)。MB-S、MB-P及MB-C以相同流速通过相应小鼠P-选择素Fc段包被培养皿时,利用平行板流动腔在不同时间点测定相应的MB-S、MB-P及MB-C(对照组)的结合数目、滚动数目以及解离时达到半数解离的剪切应力。结果MB-S结合数量前3min快速增加,其后随时间增加无明显变化,而MB-P结合数量与时间呈正相关(P〈0.05),且MB-S结合数目是MB-P的2~4倍;对照组MB-C未见明显结合(P〈0.05)。MB-S滚动数目大于MB-P(P〈0.05);MB-S半数解离时剪切力小于MB-P(P〈0.05)。结论靶向超声微泡MB-S表现为早期、快速、不稳定的结合及滚动,MB-P表现为缓慢牢固结合。 Objective To evaluate the adhesion effection of Sialyl Lewisx and anti - P - selectin monoclonal antibody targeted ultrasound microbubbles by parallel plate flow chamber. Methods The Sialyl Lewis^X (MB- S), anti- P- selectin monoclone antibody (MB- P) and isotype IgG1 (MB- C) were constructed by "avidin- biotin" respectively. The attachment and detachment of MB- S, MB - P and MB - C to P - selectin immobilized on a culture dish were assessed in a parallel - plate flow chamber. While the attachment of MB - C served as a control group. Results The bonding number of MB - S increased rapidly in first 3 min, then no obviously increased appeared in the rest time, and there was positive correlation between the bonding number of MB - P and time(P〈0.05). While the bonding number of MB - S bound was 2 - 4 times more than the number of MB-P. There was no obviously bonding of MB - C in control group (P〈0.05 ). The rolling number of MB - S was larger than that of MB - P (P〈0.05). There was limited adherence of the control group to P-selectin. Conclusion The appearance of MB - S targeted ultrasound microbul)bles is bonding and rollingearly, rapidly and unsteadily, and the appearance of MB - P is bonding slowly and firmly,
出处 《临床超声医学杂志》 2009年第3期145-148,共4页 Journal of Clinical Ultrasound in Medicine
基金 国家863计划项目(2006AA02Z478)
关键词 超声检查 微气泡 靶向 平行板流动腔 P-选择素单克隆抗体 SIALYL Lewis^X Ultrsonography Microbubbles, targeted Parallel plate flow chamber Anti- P- selectin monoclonal antibody Sialyl Eewis^x
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参考文献8

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二级参考文献2

共引文献12

同被引文献22

  • 1Bhatia SK, King MR, Hammer DA. The state diagram for cell adhesion mediated by two receptors. Biophys, 2003, 84(4): 2671-2690.
  • 2Schmitz G. Ultrasonic imaging of molecular targets. Basic Res Cardiol, 2008, 103(2): 174-181.
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  • 4Takalkar AM, Klibanov AL, Rychak JJ, et al. Binding and detachment dynamics of microbubbles targeted to P-selectin under controlled shear flow. J Control Release, 2004, 96 (3): 473-482.
  • 5Klibanov AL, Rychak J J, Yang WC, et al. Targeted ultrasound contrast agent for molecular imaging of inflammation in high-shear flow. Contrast Media Mol Imaging, 2006, 1(6): 259-266.
  • 6Marshall BT, Long M, Piper JW, et al. Direct observation of catch bonds involving cell-adhesion molecules. Nature, 2003, 423(6936): 190-193.
  • 7Eniola AO, Willcox JP, Hammer DA. Interplay between rolling and firm adhesion elucidated with a cell-free system engineered with two distinct receptor-ligand pairs. Biophys J, 2003, 85 (4): 2720-2731.
  • 8Lorz BG, Smith AS, Gege C, et al. Adhesion of giant vesicles mediated by weak binding of sialyl-lewisx to e-selectin in the presence of repelling poly (ethylene glycol) molecules. Langmuir, 2007, 23 (24): 12293-12300.
  • 9Somers WS, Tang J, Shaw GD, et al. Insights into the molecular basis of leukocyte tethering and rolling revealed by structures of P- and E-selectin bound to SLeX and PSGL-1. Cell, 2000, 103(3): 467-479.
  • 10Muro S, Dziubla T, Qiu WN, et al. Endothelial targeting of high-affinity multivalent polymer nanocarriers directed to intercellular adhesion molecule 1. JPET, 2006, 317(3): 1161-1169.

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