The Effects of Sindbis Viral Vectors on Neuronal Function
Viral vectors are attractive tools to express genes in neurons. Transduction of neurons with a recombinant, replication-deficient Sindbis viral vector is a method of choice for studying the effects of short-term protein overexpression on neuronal function. However, to which extent Sindbis by itself...
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Frontiers Media S.A.
2019-08-01
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Series: | Frontiers in Cellular Neuroscience |
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Online Access: | https://www.frontiersin.org/article/10.3389/fncel.2019.00362/full |
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English |
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Article |
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DOAJ |
author |
Seçil Uyaniker Sophie J. F. van der Spek Niels R. Reinders Niels R. Reinders Hui Xiong Hui Xiong Ka Wan Li Koen Bossers August B. Smit Joost Verhaagen Joost Verhaagen Helmut W. Kessels Helmut W. Kessels |
spellingShingle |
Seçil Uyaniker Sophie J. F. van der Spek Niels R. Reinders Niels R. Reinders Hui Xiong Hui Xiong Ka Wan Li Koen Bossers August B. Smit Joost Verhaagen Joost Verhaagen Helmut W. Kessels Helmut W. Kessels The Effects of Sindbis Viral Vectors on Neuronal Function Frontiers in Cellular Neuroscience Sindbis viral vector hippocampus transcriptomics proteomics electrophysiology |
author_facet |
Seçil Uyaniker Sophie J. F. van der Spek Niels R. Reinders Niels R. Reinders Hui Xiong Hui Xiong Ka Wan Li Koen Bossers August B. Smit Joost Verhaagen Joost Verhaagen Helmut W. Kessels Helmut W. Kessels |
author_sort |
Seçil Uyaniker |
title |
The Effects of Sindbis Viral Vectors on Neuronal Function |
title_short |
The Effects of Sindbis Viral Vectors on Neuronal Function |
title_full |
The Effects of Sindbis Viral Vectors on Neuronal Function |
title_fullStr |
The Effects of Sindbis Viral Vectors on Neuronal Function |
title_full_unstemmed |
The Effects of Sindbis Viral Vectors on Neuronal Function |
title_sort |
effects of sindbis viral vectors on neuronal function |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cellular Neuroscience |
issn |
1662-5102 |
publishDate |
2019-08-01 |
description |
Viral vectors are attractive tools to express genes in neurons. Transduction of neurons with a recombinant, replication-deficient Sindbis viral vector is a method of choice for studying the effects of short-term protein overexpression on neuronal function. However, to which extent Sindbis by itself may affect neurons is not fully understood. We assessed effects of neuronal transduction with a Sindbis viral vector on the transcriptome and proteome in organotypic hippocampal slice cultures, and analyzed the electrophysiological properties of individual CA1 neurons, at 24 h and 72 h after viral vector injection. Whereas Sindbis caused substantial gene expression alterations, changes at the protein level were less pronounced. Alterations in transcriptome and proteome were predominantly limited to proteins involved in mediating anti-viral innate immune responses. Sindbis transduction did not affect the intrinsic electrophysiological properties of individual neurons: the membrane potential and neuronal excitability were similar between transduced and non-transduced CA1 neurons up to 72 h after Sindbis injection. Synaptic currents also remained unchanged upon Sindbis transduction, unless slices were massively infected for 72 h. We conclude that Sindbis viral vectors at low transduction rates are suitable for studying short-term effects of a protein of interest on electrophysiological properties of neurons, but not for studies on the regulation of gene expression. |
topic |
Sindbis viral vector hippocampus transcriptomics proteomics electrophysiology |
url |
https://www.frontiersin.org/article/10.3389/fncel.2019.00362/full |
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doaj-233e6a5cde484e82963af248cf19de162020-11-25T01:50:13ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022019-08-011310.3389/fncel.2019.00362465688The Effects of Sindbis Viral Vectors on Neuronal FunctionSeçil Uyaniker0Sophie J. F. van der Spek1Niels R. Reinders2Niels R. Reinders3Hui Xiong4Hui Xiong5Ka Wan Li6Koen Bossers7August B. Smit8Joost Verhaagen9Joost Verhaagen10Helmut W. Kessels11Helmut W. Kessels12Laboratory for Neuroregeneration, The Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, NetherlandsDepartment of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, NetherlandsLaboratory for Neuroregeneration, The Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, NetherlandsDepartment of Cellular and Computational Neuroscience, Swammerdam Institute for Life Sciences, Amsterdam Neuroscience, University of Amsterdam, Amsterdam, NetherlandsLaboratory for Neuroregeneration, The Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, NetherlandsDepartment of Cellular and Computational Neuroscience, Swammerdam Institute for Life Sciences, Amsterdam Neuroscience, University of Amsterdam, Amsterdam, NetherlandsDepartment of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, NetherlandsLaboratory for Neuroregeneration, The Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, NetherlandsDepartment of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, NetherlandsLaboratory for Neuroregeneration, The Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, NetherlandsDepartment of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University Amsterdam, Amsterdam, NetherlandsLaboratory for Neuroregeneration, The Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, NetherlandsDepartment of Cellular and Computational Neuroscience, Swammerdam Institute for Life Sciences, Amsterdam Neuroscience, University of Amsterdam, Amsterdam, NetherlandsViral vectors are attractive tools to express genes in neurons. Transduction of neurons with a recombinant, replication-deficient Sindbis viral vector is a method of choice for studying the effects of short-term protein overexpression on neuronal function. However, to which extent Sindbis by itself may affect neurons is not fully understood. We assessed effects of neuronal transduction with a Sindbis viral vector on the transcriptome and proteome in organotypic hippocampal slice cultures, and analyzed the electrophysiological properties of individual CA1 neurons, at 24 h and 72 h after viral vector injection. Whereas Sindbis caused substantial gene expression alterations, changes at the protein level were less pronounced. Alterations in transcriptome and proteome were predominantly limited to proteins involved in mediating anti-viral innate immune responses. Sindbis transduction did not affect the intrinsic electrophysiological properties of individual neurons: the membrane potential and neuronal excitability were similar between transduced and non-transduced CA1 neurons up to 72 h after Sindbis injection. Synaptic currents also remained unchanged upon Sindbis transduction, unless slices were massively infected for 72 h. We conclude that Sindbis viral vectors at low transduction rates are suitable for studying short-term effects of a protein of interest on electrophysiological properties of neurons, but not for studies on the regulation of gene expression.https://www.frontiersin.org/article/10.3389/fncel.2019.00362/fullSindbis viral vectorhippocampustranscriptomicsproteomicselectrophysiology |