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微泡介导的声孔作用中的膜穿孔和恢复动力学。

Membrane perforation and recovery dynamics in microbubble-mediated sonoporation.

机构信息

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

出版信息

Ultrasound Med Biol. 2013 Dec;39(12):2393-405. doi: 10.1016/j.ultrasmedbio.2013.08.003. Epub 2013 Sep 21.

Abstract

Transient sonoporation can essentially be epitomized by two fundamental processes: acoustically induced membrane perforation and its subsequent resealing. To provide insight into these processes, this article presents a new series of direct evidence on the membrane-level dynamics during and after an episode of sonoporation. Our direct observations were obtained from anchored fetal fibroblasts whose membrane topography was imaged in situ using real-time confocal microscopy. To facilitate controlled sonoporation at the single-cell level, microbubbles that can passively adhere to the cell membrane were first introduced at a 1:1 cell-to-bubble ratio. Single-pulse ultrasound exposure (1-MHz frequency, 10-cycle pulse duration, 0.85-MPa peak negative pressure in situ) was then applied to trigger microbubble pulsation/collapse, which, in turn, instigated membrane perforation. With this protocol, five membrane-level phenomena were observed: (i) localized perforation of the cell membrane was synchronized with the instant of ultrasound pulsing; (ii) perforation sites with temporal peak area <30 μm(2) were resealed successfully; (iii) during recovery, a thickened pore rim emerged, and its temporal progression corresponded with the pore closure action; (iv) membrane resealing, if successful, would generally be completed within 1 min of the onset of sonoporation, and the resealing time constant was estimated to be below 20 s; (v) membrane resealing would fail for overly large pores (>100 μm(2)) or in the absence of extracellular calcium ions. These findings serve to underscore the spatiotemporal complexity of membrane-level dynamics in sonoporation.

摘要

瞬时声孔可以基本上被概括为两个基本过程

声致膜穿孔及其随后的再封闭。为了深入了解这些过程,本文提出了一系列关于声孔过程中及之后的膜水平动力学的新的直接证据。我们的直接观察结果来自锚定的胎儿成纤维细胞,其膜拓扑结构使用实时共聚焦显微镜在原位成像。为了在单细胞水平上实现受控声孔,首先以 1:1 的细胞与气泡比引入可以被动附着在细胞膜上的微泡。然后应用单脉冲超声照射(1MHz 频率、10 个周期脉冲持续时间、原位 0.85MPa 峰值负压)来触发微泡脉动/崩溃,从而引发膜穿孔。使用此方案,观察到了五个膜水平现象:(i)细胞膜的局部穿孔与超声脉冲的瞬间同步;(ii)具有时间峰值面积 <30 μm2 的穿孔部位成功再封闭;(iii)在恢复过程中,出现了增厚的孔缘,其时间进程与孔关闭动作相对应;(iv)如果成功,膜再封闭通常会在声孔作用开始后的 1 分钟内完成,并且再封闭时间常数估计低于 20s;(v)对于过大的孔(>100 μm2)或在没有细胞外钙离子的情况下,膜再封闭将失败。这些发现强调了声孔过程中膜水平动力学的时空复杂性。

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