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膜泡形成作为靶向微泡介导的位点特异性超声穿孔中的一种恢复策略。

Membrane blebbing as a recovery manoeuvre in site-specific sonoporation mediated by targeted microbubbles.

作者信息

Leow Ruen Shan, Wan Jennifer M F, Yu Alfred C H

机构信息

Medical Engineering Program, The University of Hong Kong, Pokfulam, Hong Kong.

School of Biological Sciences, The University of Hong Kong, Pokfulam, Hong Kong.

出版信息

J R Soc Interface. 2015 Apr 6;12(105). doi: 10.1098/rsif.2015.0029.

Abstract

Site-specific perforation of the plasma membrane can be achieved through ultrasound-triggered cavitation of a single microbubble positioned adjacent to the cell. However, for this perforation approach (sonoporation), the recovery manoeuvres invoked by the cell are unknown. Here, we report new findings on how membrane blebbing can be a recovery manoeuvre that may take place in sonoporation episodes whose pores are of micrometres in diameter. Each sonoporation site was created using a protocol involving single-shot ultrasound exposure (frequency: 1 MHz; pulse length: 30 cycles; peak negative pressure: 0.45 MPa) which triggered inertial cavitation of a single targeted microbubble (diameter: 1-5 µm). Over this process, live confocal microscopy was conducted in situ to monitor membrane dynamics, model drug uptake kinetics and cytoplasmic calcium ion (Ca(2+)) distribution. Results show that blebbing would occur at a recovering sonoporation site after its resealing, and it may emerge elsewhere along the membrane periphery. The bleb size was correlated with the pre-exposure microbubble diameter, and 99% of blebbing cases at sonoporation sites were inflicted by microbubbles larger than 1.5 µm diameter (analysed over 124 sonoporation episodes). Blebs were not observed at irreversible sonoporation sites or when sonoporation site repair was inhibited via extracellular Ca(2+) chelation. Functionally, the bleb volume was found to serve as a buffer compartment to accommodate the cytoplasmic Ca(2+) excess brought about by Ca(2+) influx during sonoporation. These findings suggest that membrane blebbing would help sonoporated cells restore homeostasis.

摘要

通过超声触发与细胞相邻定位的单个微泡的空化作用,可以实现质膜的位点特异性穿孔。然而,对于这种穿孔方法(声孔效应),细胞引发的恢复机制尚不清楚。在这里,我们报告了关于膜泡形成如何作为一种恢复机制的新发现,这种机制可能发生在直径为微米级孔隙的声孔效应事件中。每个声孔效应位点是通过单次超声暴露(频率:1兆赫;脉冲长度:30个周期;峰值负压:0.45兆帕)的方案创建的,该方案触发单个靶向微泡(直径:1-5微米)的惯性空化。在此过程中,进行原位实时共聚焦显微镜观察,以监测膜动力学、模拟药物摄取动力学和细胞质钙离子(Ca(2+))分布。结果表明,在恢复的声孔效应位点重新封闭后会出现膜泡形成,并且它可能出现在膜周边的其他位置。膜泡大小与暴露前微泡直径相关,在声孔效应位点99%的膜泡形成情况是由直径大于1.5微米的微泡引起的(在124次声孔效应事件中分析)。在不可逆的声孔效应位点或通过细胞外Ca(2+)螯合抑制声孔效应位点修复时未观察到膜泡。在功能上,发现膜泡体积作为一个缓冲隔室,以容纳声孔效应期间Ca(2+)流入带来的细胞质Ca(2+)过量。这些发现表明膜泡形成有助于声孔效应处理后的细胞恢复内环境稳定。

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Lipid shedding from single oscillating microbubbles.单个振荡微泡的脂质脱落。
Ultrasound Med Biol. 2014 Aug;40(8):1834-46. doi: 10.1016/j.ultrasmedbio.2014.02.031. Epub 2014 May 3.
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Single-site sonoporation disrupts actin cytoskeleton organization.单点声孔效应会破坏肌动蛋白细胞骨架的组织。
J R Soc Interface. 2014 Mar 26;11(95):20140071. doi: 10.1098/rsif.2014.0071. Print 2014 Jun 6.
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Acoustic behavior of microbubbles and implications for drug delivery.微泡的声行为及其对药物输送的影响。
Adv Drug Deliv Rev. 2014 Jun;72:28-48. doi: 10.1016/j.addr.2014.03.003. Epub 2014 Mar 23.
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Membrane perforation and recovery dynamics in microbubble-mediated sonoporation.微泡介导的声孔作用中的膜穿孔和恢复动力学。
Ultrasound Med Biol. 2013 Dec;39(12):2393-405. doi: 10.1016/j.ultrasmedbio.2013.08.003. Epub 2013 Sep 21.

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