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Luciferase therapeutic microcapsules for gene therapy
Anna Aihua Li1, Donna Y Hou, Feng Shen
1Department of Pathology & Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.
Artificial Cells, Blood Substitutes, and Immobilization Biotechnology
|November 20, 2009
Summary
Luciferase expression in microencapsulated cells can monitor cell viability and gene expression. The hybrid ubiquitin B promoter maintained signals, unlike the cytomegalovirus promoter, indicating its potential for sustained monitoring.
Area of Science:
- Biotechnology
- Cell Biology
- Biomedical Engineering
Background:
- Monitoring microencapsulated cells is crucial for assessing viability and function.
- Luciferase reporter systems offer a sensitive method for tracking biological processes.
Purpose of the Study:
- To evaluate luciferase as a reporter for monitoring gene expression and viability of encapsulated Madin-Darby Canine Kidney (MDCK) cells.
- To compare the stability of luciferase expression driven by different promoters (CMV and UbB) in encapsulated cells.
Main Methods:
- MDCK cells engineered for luciferase expression (CMV or UbB promoter) were encapsulated in alginate-poly-L-lysine-alginate microcapsules.
- In vitro and in vivo experiments quantified luciferase signals from encapsulated cells.
- Cell viability was assessed post-implantation.
Main Results:
- Luciferase signals correlated linearly with the number of encapsulated cells.
- CMV-driven expression showed a rapid signal decrease post-implantation, while UbB-driven expression remained stable.
- Encapsulated cells maintained good viability despite signal fluctuations.
Conclusions:
- Luciferase serves as a viable marker for monitoring microencapsulated cells.
- The UbB promoter demonstrates superior stability for long-term reporter gene expression in encapsulated cell systems.
- This approach enables quantitative assessment of cell viability and gene expression in biomedical applications.
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