Delivery of Condensed DNA by Liposomal Non-viral Gene Delivery System into Nucleus of Dendritic Cells
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- Nakamura Takashi
- Graduate School of Pharmaceutical Sciences, Hokkaido University Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST)
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- Moriguchi Rumiko
- Graduate School of Pharmaceutical Sciences, Hokkaido University Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST)
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- Kogure Kentaro
- Graduate School of Pharmaceutical Sciences, Hokkaido University Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST)
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- Minoura Arisa
- Graduate School of Pharmaceutical Sciences, Hokkaido University
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- Masuda Tomoya
- Graduate School of Pharmaceutical Sciences, Hokkaido University Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST)
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- Akita Hidetaka
- Graduate School of Pharmaceutical Sciences, Hokkaido University Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST)
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- Kato Kazunori
- Department of Molecular Medicine, Sapporo Medical University
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- Hamada Hirofumi
- Department of Molecular Medicine, Sapporo Medical University
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- Ueno Masaharu
- Faculty of Pharmaceutical Sciences, University of Toyama
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- Futaki Shiroh
- Institute for Chemical Research, Kyoto University Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST)
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- Harashima Hideyoshi
- Graduate School of Pharmaceutical Sciences, Hokkaido University Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST)
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Abstract
In this study, we developed novel double-membranous non-viral gene delivery system modified with SV-40 T antigen-derived nuclear localization signal (NLS-DMEND) for delivery of luciferase plasmid DNA to nucleus of non-dividing mouse bone marrow-derived dendritic cells (BMDC). Intracellular trafficking and gene expression of NLS-DMEND in the BMDC were evaluated. Condensed DNA was observed in the nucleus by confocal laser scanning microscopy, and the NLS-DMEND induced significant luciferase activity in the BMDC. It was suggested that the condensed DNA particle transferred into nucleus via energy dependent manner, since the nuclear transfer was inhibited by metabolic inhibitors. In conclusion, condensed plasmid DNA was delivered into the nucleus of non-dividing BMDC by NLS-DMEND.
Journal
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- Biological and Pharmaceutical Bulletin
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Biological and Pharmaceutical Bulletin 29 (6), 1290-1293, 2006
The Pharmaceutical Society of Japan
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Details 詳細情報について
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- CRID
- 1390282679604257664
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- NII Article ID
- 110005602287
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- NII Book ID
- AA10885497
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- ISSN
- 13475215
- 09186158
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- NDL BIB ID
- 7921905
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed