The establishment of gene delivery systems that result in efficient transfection of the pancreatic β-cells may generate an important tool for the study of IDDM and may also represent one critical step toward a clinical application of gene transfer for the prevention or early treatment of the disease. Using the reporter gene vectors pCAT and pCMV β-gal, we have investigated the efficiency of transfection mediated by calcium phosphate precipitation, the monocationic liposome Lipofectin, the polycationic liposome Lipofectamine, and adenovirus-polylysine (AdpL) DNA complexes in human, mouse, rat, and fetal porcine islet cells. In all species studied, calcium phosphate–mediated transfection resulted in lower chloramphenicol acetyl transferase (CAT) activities than the other methods. Intact human, mouse, and rat islets were poorly transfected by Lipofectin, Lipofectamine, and AdpL. When dispersed by trypsin treatment, however, human, mouse, rat, and fetal pig islet cells were efficiently transfected by Lipofectamine. Moreover, transfection of dispersed human and mouse islet cells using AdpL also resulted in high CAT activities. The percentage of cells staining positively for β-galactosidase after transfection with Lipofectamine was 49% for mouse, 56% for rat, and 57% for dispersed human islet cells. Transfection of human islet cells using AdpL, however, yielded 70% βgal–positive cells. Fluorescence-activated cell sorting-purified rat islet α- and β-cells were transfected with similar efficiency using Lipofectamine. CAT expression in human islet cells transfected with either Lipofectamine or AdpL reached a peak value after 5–7 days, followed by a gradual decline. It is concluded that transfection with AdpL or Lipofectamine are both efficient means to achieve transient expression of gene constructs in human and mouse islet cells, while for rat and fetal porcine islet cells, Lipofectamine is the most efficient of the agents investigated in this study.
Original Articles|
September 01 1996
Efficient Gene Transfer to Dispersed Human Pancreatic Islet Cells In Vitro Using Adenovirus-Polylysine/DNA Complexes or Polycationic Liposomes
Johan Saldeen;
Johan Saldeen
Department of Medical Cell Biology, Uppsala University
Biomedicum, Uppsala, Sweden
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David T Curiel;
David T Curiel
Department of Medicine, University of Alabama at Birmingham
Birmingham, Alabama
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Décio L Eizirik;
Décio L Eizirik
Department of Medical Cell Biology, Uppsala University
Biomedicum, Uppsala, Sweden
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Arne Andersson;
Arne Andersson
Department of Medical Cell Biology, Uppsala University
Biomedicum, Uppsala, Sweden
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Eva Strandell;
Eva Strandell
Bartholin Instittutet, Kommunehospitalet
Copenhagen, Denmark
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Karsten Buschard;
Karsten Buschard
Bartholin Instittutet, Kommunehospitalet
Copenhagen, Denmark
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Nils Welsh
Nils Welsh
Department of Medical Cell Biology, Uppsala University
Biomedicum, Uppsala, Sweden
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Address correspondence and reprint requests to Dr. Nils Welsh, Department of Medical Cell Biology, P.O. Box 571, Biomedicum, S-751 23 Uppsala, Sweden.
Diabetes 1996;45(9):1197–1203
Article history
Received:
July 26 1995
Revision Received:
April 04 1996
Accepted:
April 04 1996
PubMed:
8772722
Citation
Johan Saldeen, David T Curiel, Décio L Eizirik, Arne Andersson, Eva Strandell, Karsten Buschard, Nils Welsh; Efficient Gene Transfer to Dispersed Human Pancreatic Islet Cells In Vitro Using Adenovirus-Polylysine/DNA Complexes or Polycationic Liposomes. Diabetes 1 September 1996; 45 (9): 1197–1203. https://doi.org/10.2337/diab.45.9.1197
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