Virally mediated gene manipulation in the adult CNS

Understanding how the CNS functions poses one of the greatest challenges in modern life science and medicine. Studying the brain is especially challenging because of its complexity, the heterogeneity of its cellular composition, and the substantial changes it undergoes throughout its life-span. The...

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Main Authors: Efrat eEdry, Raphael eLamprecht, Shlomo eWagner, Kobi eRosenblum
Format: Article
Language:English
Published: Frontiers Media S.A. 2011-12-01
Series:Frontiers in Molecular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnmol.2011.00057/full
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spelling doaj-79c6e7cac1e840f2aed278abb6b836b12020-11-24T23:42:19ZengFrontiers Media S.A.Frontiers in Molecular Neuroscience1662-50992011-12-01410.3389/fnmol.2011.0005711583Virally mediated gene manipulation in the adult CNSEfrat eEdry0Raphael eLamprecht1Shlomo eWagner2Kobi eRosenblum3Haifa UniversityHaifa UniversityHaifa UniversityHaifa UniversityUnderstanding how the CNS functions poses one of the greatest challenges in modern life science and medicine. Studying the brain is especially challenging because of its complexity, the heterogeneity of its cellular composition, and the substantial changes it undergoes throughout its life-span. The complexity of adult-brain neural networks results also from the diversity of properties and functions of neuronal cells, governed, inter alia, by temporally and spatially differential expression of proteins in mammalian brain cell populations. Hence, research into the biology of CNS activity and its implications to human and animal behavior must use novel scientific tools. One source of such tools is the field of molecular genetics – recently utilized more and more frequently in neuroscience research. Transgenic approaches in general, and gene targeting in rodents have become fundamental tools for elucidating gene function in the CNS. Although spectacular progress has been achieved over recent decades by using these approaches, it is important to note that they face a number of restrictions. One of the main challenges is presented by the temporal and spatial regulation of introduced genetic manipulations. Viral vectors provide an alternative approach to temporally regulated, localized delivery of genetic modifications into neurons. In this review we describe available technologies for gene transfer into the adult mammalian CNS that use both viral and non-viral tools. We discuss viral vectors frequently used in neuroscience, with emphasis on lentiviral vector (LV) systems. We consider adverse effects of LVs, and the use of LVs for temporally and spatially controllable manipulations. Especially, we highlight the significance of viral vector-mediated genetic manipulations in studying learning and memory processes, and how they may be effectively used to separate out the various phases of learning: acquisition, consolidation, retrieval, and maintenance.http://journal.frontiersin.org/Journal/10.3389/fnmol.2011.00057/fullgene regulationlearning and memoryviral vectorsLentivirus (LV)
collection DOAJ
language English
format Article
sources DOAJ
author Efrat eEdry
Raphael eLamprecht
Shlomo eWagner
Kobi eRosenblum
spellingShingle Efrat eEdry
Raphael eLamprecht
Shlomo eWagner
Kobi eRosenblum
Virally mediated gene manipulation in the adult CNS
Frontiers in Molecular Neuroscience
gene regulation
learning and memory
viral vectors
Lentivirus (LV)
author_facet Efrat eEdry
Raphael eLamprecht
Shlomo eWagner
Kobi eRosenblum
author_sort Efrat eEdry
title Virally mediated gene manipulation in the adult CNS
title_short Virally mediated gene manipulation in the adult CNS
title_full Virally mediated gene manipulation in the adult CNS
title_fullStr Virally mediated gene manipulation in the adult CNS
title_full_unstemmed Virally mediated gene manipulation in the adult CNS
title_sort virally mediated gene manipulation in the adult cns
publisher Frontiers Media S.A.
series Frontiers in Molecular Neuroscience
issn 1662-5099
publishDate 2011-12-01
description Understanding how the CNS functions poses one of the greatest challenges in modern life science and medicine. Studying the brain is especially challenging because of its complexity, the heterogeneity of its cellular composition, and the substantial changes it undergoes throughout its life-span. The complexity of adult-brain neural networks results also from the diversity of properties and functions of neuronal cells, governed, inter alia, by temporally and spatially differential expression of proteins in mammalian brain cell populations. Hence, research into the biology of CNS activity and its implications to human and animal behavior must use novel scientific tools. One source of such tools is the field of molecular genetics – recently utilized more and more frequently in neuroscience research. Transgenic approaches in general, and gene targeting in rodents have become fundamental tools for elucidating gene function in the CNS. Although spectacular progress has been achieved over recent decades by using these approaches, it is important to note that they face a number of restrictions. One of the main challenges is presented by the temporal and spatial regulation of introduced genetic manipulations. Viral vectors provide an alternative approach to temporally regulated, localized delivery of genetic modifications into neurons. In this review we describe available technologies for gene transfer into the adult mammalian CNS that use both viral and non-viral tools. We discuss viral vectors frequently used in neuroscience, with emphasis on lentiviral vector (LV) systems. We consider adverse effects of LVs, and the use of LVs for temporally and spatially controllable manipulations. Especially, we highlight the significance of viral vector-mediated genetic manipulations in studying learning and memory processes, and how they may be effectively used to separate out the various phases of learning: acquisition, consolidation, retrieval, and maintenance.
topic gene regulation
learning and memory
viral vectors
Lentivirus (LV)
url http://journal.frontiersin.org/Journal/10.3389/fnmol.2011.00057/full
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