Gaussia Luciferase Reporter Assay for Assessment of Gene Delivery Systems in Vivo
Chinese Medical Sciences JournalIssue 2, Pages: 95-99(2010)
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Gaussia Luciferase Reporter Assay for Assessment of Gene Delivery Systems in Vivo
Affiliations:
National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College,Beijing,China,100005
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Published Online:10 June 2010,
Published:2010
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Feng Chen, Zhen Xu, Jing Lu, et al. Gaussia Luciferase Reporter Assay for Assessment of Gene Delivery Systems in Vivo[J]. Chinese medical sciences journal, 2010, (2): 95-99.
DOI:
Feng Chen, Zhen Xu, Jing Lu, et al. Gaussia Luciferase Reporter Assay for Assessment of Gene Delivery Systems in Vivo[J]. Chinese medical sciences journal, 2010, (2): 95-99.DOI:
Gaussia Luciferase Reporter Assay for Assessment of Gene Delivery Systems in Vivo
Objective To develop an alternative method for assessment of gene delivery systems in vivo. Methods Mouse primary spleen lymphocytes were genetically modified in vitro by a retroviral vector harboring a Gaussia luciferase (Gluc) expression cassette. After implantation of these cells into recipient mice
the expression of Gluc was detected in whole blood or plasma collected. Results As little as 10 uL whole blood drawn from the recipient mice could guarantee prompt reading of Gluc activity with a luminometer. And the reading was found in good correlation with the number of genetically modified spleen lymphocytes implanted to the mice. Conclusions Gluc may be useful as an in vivo reporter for gene therapy researches
and Gluc blood assay could provide an alternative method for assessment of gene delivery systems in vivo.
Abstract
Objective To develop an alternative method for assessment of gene delivery systems in vivo. Methods Mouse primary spleen lymphocytes were genetically modified in vitro by a retroviral vector harboring a Gaussia luciferase (Gluc) expression cassette. After implantation of these cells into recipient mice
the expression of Gluc was detected in whole blood or plasma collected. Results As little as 10 uL whole blood drawn from the recipient mice could guarantee prompt reading of Gluc activity with a luminometer. And the reading was found in good correlation with the number of genetically modified spleen lymphocytes implanted to the mice. Conclusions Gluc may be useful as an in vivo reporter for gene therapy researches
and Gluc blood assay could provide an alternative method for assessment of gene delivery systems in vivo.