共 71 条
Cell-cycle-specific Cellular Responses to Sonoporation
被引:45
作者:
Fan, Pengfei
[1
]
Zhang, Yi
[1
]
Guo, Xiasheng
[1
]
Cai, Chenliang
[1
]
Wang, Maochen
[1
]
Yang, Dongxin
[1
]
Li, Yiran
[2
]
Tu, Juan
[1
]
Crum, Lawrence A.
[3
]
Wu, Junru
[4
]
Zhang, Dong
[1
,5
]
机构:
[1] Nanjing Univ, Minist Educ, Key Lab Modern Acoust, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, Dept Phys, Collaborat Innovat Ctr Adv Microstruct, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
[3] Univ Washington, Ctr Ind & Med Ultrasound, Seattle, WA 98105 USA
[4] Univ Vermont, Dept Phys, Burlington, VT 05405 USA
[5] Chinese Acad Sci, State Key Lab Acoust, Beijing 10080, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
Microbubble-mediated sonoporation;
cell cycle;
membrane permeabilization;
cytoskeleton disassembly;
bubble-cell-interaction;
MEDIATED DNA TRANSFECTION;
DRUG-DELIVERY;
IN-VITRO;
GENE DELIVERY;
ULTRASOUND;
MICROBUBBLE;
MEMBRANE;
THERAPY;
NANOPARTICLES;
CHECKPOINTS;
D O I:
10.7150/thno.20820
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Microbubble-mediated sonoporation has shown its great potential in facilitating intracellular uptake of gene/drugs and other therapeutic agents that are otherwise difficult to enter cells. However, the biophysical mechanisms underlying microbubble-cell interactions remain unclear. Particularly, it is still a major challenge to get a comprehensive understanding of the impact of cell cycle phase on the cellular responses simultaneously occurring in cell membrane and cytoskeleton induced by microbubble sonoporation. Methods: Here, efficient synchronizations were performed to arrest human cervical epithelial carcinoma (HeLa) cells in individual cycle phases. The, topography and stiffness of synchronized cells were examined using atomic force microscopy. The variations in cell membrane permeabilization and cytoskeleton arrangement induced by sonoporation were analyzed simultaneously by a real-time fluorescence imaging system. Results: The results showed that G1-phase cells typically had the largest height and elastic modulus, while S-phase cells were generally the flattest and softest ones. Consequently, the S-Phase was found to be the preferred cycle for instantaneous sonoporation treatment, due to the greatest enhancement of membrane permeability and the fastest cytoskeleton disassembly at the early stage after sonoporation. Conclusion: The current findings may benefit ongoing efforts aiming to pursue rational utilization of microbubble-mediated sonoporation in cell cycle-targeted gene/drug delivery for cancer therapy.
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页码:4894 / 4908
页数:15
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