Evaluation of Long-Term Gene Expression in Mouse Liver Using PhiC31 Integrase and Hydrodynamic Injection
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- Umemoto Yoshiaki
- Department of Drug Delivery Research, Graduate School of Pharmaceutical Sciences, Kyoto University
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- Kawakami Shigeru
- Department of Drug Delivery Research, Graduate School of Pharmaceutical Sciences, Kyoto University
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- Otani Yuki
- Department of Drug Delivery Research, Graduate School of Pharmaceutical Sciences, Kyoto University
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- Higuchi Yuriko
- Department of Drug Delivery Research, Graduate School of Pharmaceutical Sciences, Kyoto University
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- Yamashita Fumiyoshi
- Department of Drug Delivery Research, Graduate School of Pharmaceutical Sciences, Kyoto University
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- Hashida Mitsuru
- Department of Drug Delivery Research, Graduate School of Pharmaceutical Sciences, Kyoto University Institute for Integrated Cell-Material Sciences, Kyoto University
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抄録
PhiC31 integrase has the potential to achieve long-term transgene expression because of site-specific and unidirectional recombination. In this study, plasmid DNA (pDNA) encoding Gaussia luciferase (Gluc) cDNA was constructed and the optimal condition for long-term gene expression using phiC31 integrase in mouse liver after hydrodynamic injection was investigated. Gluc is secreted and thus allows quantification of its expression level in blood and easy determination of the expression time-course. Mice were co-transfected with 25 µg donor pDNA (pORF-Gluc/attB) and different amounts of helper pDNA (pCMV-int; from 1 to 50 µg). Serum Gluc expression was evaluated during 120 d. The most highly sustained gene expression was obtained when 10 µg of helper pDNA was co-transfected in ICR and C57BL/6 mice. However, the Gluc expression in C57BL/6 mice was slightly lower and less durable than that in ICR mice. Little hepatic damage caused by phiC31 integrase was observed during 120 d in ICR and C57BL/6 mice.
収録刊行物
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- Biological & Pharmaceutical Bulletin
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Biological & Pharmaceutical Bulletin 35 (7), 1182-1186, 2012
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390001204631792384
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- NII論文ID
- 130001872117
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- NII書誌ID
- AA10885497
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- COI
- 1:STN:280:DC%2BC38jps1Omug%3D%3D
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- ISSN
- 13475215
- 09186158
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- NDL書誌ID
- 023766000
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- PubMed
- 22791170
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
- KAKEN
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- 抄録ライセンスフラグ
- 使用不可