Effects of extracellular matrix rigidity on sonoporation facilitated by targeted microbubbles: Bubble attachment, bubble dynamics, and cell membrane permeabilization

• Published in: Ultrasonics sonochemistry 2020-10, Vol.67, p.105125-105125, Article 105125
• Main Authors: Rong, Ning, Zhang, Meiru, Wang, Yulin, Wu, Hao, Qi, Hui, Fu, Xing, Li, Dachao, Yang, Chunmei, Wang, Yan, Fan, Zhenzhen
• Format: Article
• Language: English
• Subjects: Animals; Bubble dynamics; Cell Membrane Permeability; Extracellular Matrix - chemistry; Extracellular matrix rigidity; Fluorescence; Mice; Microbubbles; NIH 3T3 Cells; Sonication - methods; Sonoporation; Targeted microbubbles; Ultrasound
• ISSN: 1350-4177; 1873-2828
• DOI: 10.1016/j.ultsonch.2020.105125

•Dual fluorescence channels high contrast imaging strategy to resolve attachment.•Stronger attachment between targeted microbubbles and cell membrane on rigid ECM.•Total six different attachment configurations were observed.•More violent bubble oscillation driven by ultrasound for cells on rigid ECM.•Smaller pore with slower resealing process was generated to cells on rigid ECM. In this study, we investigated the effects of extracellular matrix rigidity, an important physical property of microenvironments regulating cell morphology and functions, on sonoporation facilitated by targeted microbubbles, highlighting the role of microbubbles. We conducted mechanistic studies at the cellular level on physiologically relevant soft and rigid substrates. By developing a unique imaging strategy, we first resolved details of the 3D attachment configurations between targeted microbubbles and cell membrane. High-speed video microscopy then unveiled bubble dynamics driven by a single ultrasound pulse. Finally, we evaluated the cell membrane permeabilization using a small molecule model drug. Our results demonstrate that: (1) stronger targeted microbubble attachment was formed for cells cultured on the rigid substrate, while six different attachment configurations were revealed in total; (2) more violent bubble oscillation was observed for cells cultured on the rigid substrate, while one third of bubbles attached to cells on the soft substrate exhibited deformation shortly after ultrasound was turned off; (3) higher acoustic pressure was needed to permeabilize the cell membrane for cells on the soft substrate, while under the same ultrasound condition, acoustically-activated microbubbles generated larger pores as compared to cells cultured on the soft substrate. The current findings provide new insights to understand the underlying mechanisms of sonoporation in a physiologically relevant context and may be useful for the clinical translation of sonoporation.