Gene Transfer into Neurons from Hippocampal Slices: Comparison of Recombinant Semliki Forest Virus, Adenovirus, Adeno-Associated Virus, Lentivirus, and Measles Virus

Viral vectors are useful for transferring genes into neurons. Here, we characterized recombinant Semliki Forest virus (SFV), adenovirus type 5 (Ad5), adeno-associated virus type 2 (AAV), lentivirus, and measles virus (MV) by their expression of green fluorescent protein (GFP) in rat hippocampal slic...

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Published inMolecular and cellular neuroscience Vol. 17; no. 5; pp. 855 - 871
Main Authors Ehrengruber, Markus U., Hennou, Sonia, Büeler, Hansruedi, Naim, Hussein Y., Déglon, Nicole, Lundstrom, Kenneth
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.05.2001
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Abstract Viral vectors are useful for transferring genes into neurons. Here, we characterized recombinant Semliki Forest virus (SFV), adenovirus type 5 (Ad5), adeno-associated virus type 2 (AAV), lentivirus, and measles virus (MV) by their expression of green fluorescent protein (GFP) in rat hippocampal slice cultures. SFV infected more neurons (>90% of all GFP-positive cells) than AAV, lentivirus, and MV (71, 69, and 62%, respectively), whereas no infected neurons were identified with Ad5. AAV-mediated GFP expression was neuron-specific when the platelet-derived growth factor β-chain promoter rather than cytomegalovirus promoter was used. Transgene expression occurred rapidly but transiently for SFV, increased slowly but remained stable with AAV and lentivirus, and was fast with MV. Resting membrane potential and conductance, action potentials, firing accommodation, and H-current appeared normal in infected CA1 pyramidal cells. Thus, SFV is useful for short-term and AAV and lentivirus for long-term transduction of hippocampal slices, while MV constitutes a novel vector.
AbstractList Viral vectors are useful for transferring genes into neurons. Here, we characterized recombinant Semliki Forest virus (SFV), adenovirus type 5 (Ad5), adeno-associated virus type 2 (AAV), lentivirus, and measles virus (MV) by their expression of green fluorescent protein (GFP) in rat hippocampal slice cultures. SFV infected more neurons (>90% of all GFP-positive cells) than AAV, lentivirus, and MV (71, 69, and 62%, respectively), whereas no infected neurons were identified with Ad5. AAV-mediated GFP expression was neuron-specific when the platelet-derived growth factor beta -chain promoter rather than cytomegalovirus promoter was used. Transgene expression occurred rapidly but transiently for SFV, increased slowly but remained stable with AAV and lentivirus, and was fast with MV. Resting membrane potential and conductance, action potentials, firing accommodation, and H-current appeared normal in infected CA1 pyramidal cells. Thus, SFV is useful for short-term and AAV and lentivirus for long-term transduction of hippocampal slices, while MV constitutes a novel vector. Copyright 2001 Academic Press.
Viral vectors are useful for transferring genes into neurons. Here, we characterized recombinant Semliki Forest virus (SFV), adenovirus type 5 (Ad5), adeno-associated virus type 2 (AAV), lentivirus, and measles virus (MV) by their expression of green fluorescent protein (GFP) in rat hippocampal slice cultures. SFV infected more neurons (>90% of all GFP-positive cells) than AAV, lentivirus, and MV (71, 69, and 62%, respectively), whereas no infected neurons were identified with Ad5. AAV-mediated GFP expression was neuron-specific when the platelet-derived growth factor beta-chain promoter rather than cytomegalovirus promoter was used. Transgene expression occurred rapidly but transiently for SFV, increased slowly but remained stable with AAV and lentivirus, and was fast with MV. Resting membrane potential and conductance, action potentials, firing accommodation, and H-current appeared normal in infected CA1 pyramidal cells. Thus, SFV is useful for short-term and AAV and lentivirus for long-term transduction of hippocampal slices, while MV constitutes a novel vector.
Viral vectors are useful for transferring genes into neurons. Here, we characterized recombinant Semliki Forest virus (SFV), adenovirus type 5 (Ad5), adeno-associated virus type 2 (AAV), lentivirus, and measles virus (MV) by their expression of green fluorescent protein (GFP) in rat hippocampal slice cultures. SFV infected more neurons (>90% of all GFP-positive cells) than AAV, lentivirus, and MV (71, 69, and 62%, respectively), whereas no infected neurons were identified with Ad5. AAV-mediated GFP expression was neuron-specific when the platelet-derived growth factor β-chain promoter rather than cytomegalovirus promoter was used. Transgene expression occurred rapidly but transiently for SFV, increased slowly but remained stable with AAV and lentivirus, and was fast with MV. Resting membrane potential and conductance, action potentials, firing accommodation, and H-current appeared normal in infected CA1 pyramidal cells. Thus, SFV is useful for short-term and AAV and lentivirus for long-term transduction of hippocampal slices, while MV constitutes a novel vector.
Viral vectors are useful for transferring genes into neurons. Here, we characterized recombinant Semliki Forest virus (SFV), adenovirus type 5 (Ad5), adeno-associated virus type 2 (AAV), lentivirus, and measles virus (MV) by their expression of green fluorescent protein (GFP) in rat hippocampal slice cultures. SFV infected more neurons (>90% of all GFP-positive cells) than AAV, lentivirus, and MV (71, 69, and 62%, respectively), whereas no infected neurons were identified with Ad5. AAV-mediated GFP expression was neuron-specific when the platelet-derived growth factor beta-chain promoter rather than cytomegalovirus promoter was used. Transgene expression occurred rapidly but transiently for SFV, increased slowly but remained stable with AAV and lentivirus, and was fast with MV. Resting membrane potential and conductance, action potentials, firing accommodation, and H-current appeared normal in infected CA1 pyramidal cells. Thus, SFV is useful for short-term and AAV and lentivirus for long-term transduction of hippocampal slices, while MV constitutes a novel vector.
Author Naim, Hussein Y.
Büeler, Hansruedi
Ehrengruber, Markus U.
Lundstrom, Kenneth
Déglon, Nicole
Hennou, Sonia
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  fullname: Hennou, Sonia
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  givenname: Hansruedi
  surname: Büeler
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  givenname: Hussein Y.
  surname: Naim
  fullname: Naim, Hussein Y.
  organization: Institute of Molecular Biology, University of Zurich, Winterthurerstrasse 190, CH-8057, Zurich, Switzerland
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  givenname: Kenneth
  surname: Lundstrom
  fullname: Lundstrom, Kenneth
  organization: F. Hoffmann–La Roche, Research Laboratories, CH-4070, Basel, Switzerland
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Snippet Viral vectors are useful for transferring genes into neurons. Here, we characterized recombinant Semliki Forest virus (SFV), adenovirus type 5 (Ad5),...
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SubjectTerms Adeno-associated virus
Adenoviridae - genetics
Adenoviridae - pathogenicity
Adenovirus
Animals
Cell Survival - genetics
Dependovirus - genetics
Dependovirus - pathogenicity
Gene Expression Regulation, Viral - physiology
Gene Transfer Techniques
Genetic Vectors - physiology
Green Fluorescent Proteins
Hippocampus - cytology
Hippocampus - metabolism
Hippocampus - virology
Indicators and Reagents - metabolism
Lentivirus
Lentivirus - genetics
Lentivirus - pathogenicity
Luminescent Proteins - metabolism
Measles virus
Measles virus - genetics
Measles virus - pathogenicity
Membrane Potentials - genetics
Neurons - cytology
Neurons - metabolism
Neurons - virology
Organ Culture Techniques
Pyramidal Cells - cytology
Pyramidal Cells - physiology
Pyramidal Cells - virology
Rats
Semliki Forest virus
Semliki forest virus - genetics
Semliki forest virus - pathogenicity
Time Factors
Transduction, Genetic - methods
Transgenes - physiology
Virulence - genetics
Viruses - genetics
Viruses - pathogenicity
Title Gene Transfer into Neurons from Hippocampal Slices: Comparison of Recombinant Semliki Forest Virus, Adenovirus, Adeno-Associated Virus, Lentivirus, and Measles Virus
URI https://dx.doi.org/10.1006/mcne.2001.0982
https://www.ncbi.nlm.nih.gov/pubmed/11358483
https://search.proquest.com/docview/17891251
https://search.proquest.com/docview/70859911
Volume 17
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