Volume 10, Issue 12 pp. 1723-1731
Full Article

Intracellular localization and delivery of plasmid DNA by biodegradable microsphere-mediated femtosecond laser optoporation

Atsuhiro Ishii

Atsuhiro Ishii

School of Integrated Design Engineering, Keio University, 3–14-1 Hiyoshi, Kohoku-ku, Yokohama, 223-8522 Japan

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Yuki Hiruta

Yuki Hiruta

Faculty of Pharmacy, Keio University, 1–5-30 Shibakoen, Minato, Tokyo, 105-8512 Japan

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Dag Heinemann

Dag Heinemann

Industrial and Biomedical Optics Department, Laser Zentrum Hannover e.V., Hollerithallee 8, Hannover, D-30149 Germany

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Alexander Heisterkamp

Alexander Heisterkamp

Industrial and Biomedical Optics Department, Laser Zentrum Hannover e.V., Hollerithallee 8, Hannover, D-30149 Germany

Institute of Quantum Optics, Gottfried Wilhelm Leibniz University Hannover, Am Welfengarten 1, Hannover, 30167 Germany

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Hideko Kanazawa

Hideko Kanazawa

Faculty of Pharmacy, Keio University, 1–5-30 Shibakoen, Minato, Tokyo, 105-8512 Japan

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Mitsuhiro Terakawa

Corresponding Author

Mitsuhiro Terakawa

School of Integrated Design Engineering, Keio University, 3–14-1 Hiyoshi, Kohoku-ku, Yokohama, 223-8522 Japan

Department of Electronics and Electrical Engineering, Keio University, 3–14-1 Hiyoshi, Kohoku-ku, Yokohama, 223-8522 Japan

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First published: 02 May 2017
Citations: 10

Abstract

Micro-/nanosphere-mediated femtosecond laser cell perforation is one of the high throughput technologies used for macro-molecule-delivery into multiple cells. We have demonstrated the delivery of plasmid-DNA/liposome complexes into cells using biodegradable polymer microspheres and a femtosecond laser and investigated the intracellular localization of the complexes by delivering fluorescence-labeled plasmid-DNA/liposome complexes into cells. The utilization of liposomes increases the number of complexes delivered into the cytoplasm by laser illumination, which contributed to the increased transfection rate. In the experiment involving polystyrene (PS) microspheres of different diameters, the fluorescence of the complexes was detected in the nucleus as well as cytoplasm after laser illumination for PS microspheres of 3.0 μm diameter. The direct delivery of complexes into the nucleus is probably attributed to the enhancement of the nuclear membrane permeability by the enhanced optical field obtained close to the nucleus. These revelations on the intracellular localization of foreign DNA would provide effective laser-based transfection. Picture: Intranuclear delivery of plasmid-DNA/liposome complexes by utilizing dielectric microspheres and a femtosecond laser.

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