4.5 Article

PLASMA MEMBRANE BLEBBING DYNAMICS INVOLVED IN THE REVERSIBLY PERFORATED CELL BY ULTRASOUND-DRIVEN MICROBUBBLES

期刊

ULTRASOUND IN MEDICINE AND BIOLOGY
卷 47, 期 3, 页码 733-750

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ultrasmedbio.2020.11.029

关键词

Ultrasound; Microbubble; Sonoporation; Blebbing dynamics; Drug delivery

资金

  1. National Natural Science Foundation of China [12074255, 31630007]
  2. Program of Medicine and Engineering Cross Fund of Shanghai Jiao Tong University [YG2019ZDA27, ZH2018QNA21]
  3. SMC Rising Star Fund of Shanghai Jiao Tong University [16X100080028]

向作者/读者索取更多资源

During the recovery of sonoporated cells, localized blebs undergo nucleation, expansion, pausing and retraction on a time scale of tens of seconds to minutes, which are specifically involved in reversibly sonoporated cells. The blebs spatially correlate with the membrane perforation site and temporally lag the resealing of perforated membrane. The diameter and lifetime of the blebs positively correlate with the degree of sonoporation, and intracellular calcium transients might be an upstream signal for triggering blebbing nucleation.
The perforation of plasma membrane by ultrasound-driven microbubbles (i.e., sonoporation) provides a temporary window for transporting macromolecules into the cytoplasm that is promising with respect to drug delivery and gene therapy. To improve the efficacy of delivery while ensuring biosafety, membrane resealing and cell recovery are required to help sonoporated cells defy membrane injury and regain their normal function. Blebs are found to accompany the recovery of sonoporated cells. However, the spatiotemporal characteristics of blebs and the underlying mechanisms remain unclear. With a customized platform for ultrasound exposure and 2-D/3-D live single-cell imaging, localized membrane perforation was induced with ultrasound-driven microbubbles, and the cellular responses were monitored using multiple fluorescent probes. The results indicated that localized blebs undergoing four phases (nucleation, expansion, pausing and retraction) on a time scale of tens of seconds to minutes were specifically involved in the reversibly sonoporated cells. The blebs spatially correlated with the membrane perforation site and temporally lagged (about tens of seconds to minutes) the resealing of perforated membrane. Their diameter (about several microns) and lifetime (about tens of seconds to minutes) positively correlated with the degree of sonoporation. Further studies revealed that intracellular calcium transients might be an upstream signal for triggering blebbing nucleation; exocytotic lysosomes not only contributed to resealing of the perforated membrane, but also to the increasing bleb volume during expansion; and actin components accumulation facilitated bleb retraction. These results provide new insight into the short-term strategies that the sonoporated cell employs to recover on membrane perforation and to remodel membrane structure and a biophysical foundation for sonoporation-based therapy. (E-mail: pqin@sjtu.edu.cn) (C) 2020 World Federation for Ultrasound in Medicine & Biology. Published by Elsevier Inc. All rights reserved.

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