An adeno-associated virus-based intracellular sensor of pathological nuclear factor-κB activation for disease-inducible gene transfer.

Stimulation of resident cells by NF-κB activating cytokines is a central element of inflammatory and degenerative disorders of the central nervous system (CNS). This disease-mediated NF-κB activation could be used to drive transgene expression selectively in affected cells, using adeno-associated vi...

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Autores principales: Abdelwahed Chtarto, Olivier Bockstael, Elias Gebara, Katia Vermoesen, Catherine Melas, Catherine Pythoud, Marc Levivier, Olivier De Witte, Ruth Luthi-Carter, Ralph Clinkers, Liliane Tenenbaum
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Publicado: Public Library of Science (PLoS) 2013
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spelling oai:doaj.org-article:0f6019a6b6fb4efd9ffa751341864edc2021-11-18T08:02:46ZAn adeno-associated virus-based intracellular sensor of pathological nuclear factor-κB activation for disease-inducible gene transfer.1932-620310.1371/journal.pone.0053156https://doaj.org/article/0f6019a6b6fb4efd9ffa751341864edc2013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23301037/?tool=EBIhttps://doaj.org/toc/1932-6203Stimulation of resident cells by NF-κB activating cytokines is a central element of inflammatory and degenerative disorders of the central nervous system (CNS). This disease-mediated NF-κB activation could be used to drive transgene expression selectively in affected cells, using adeno-associated virus (AAV)-mediated gene transfer. We have constructed a series of AAV vectors expressing GFP under the control of different promoters including NF-κB -responsive elements. As an initial screen, the vectors were tested in vitro in HEK-293T cells treated with TNF-α. The best profile of GFP induction was obtained with a promoter containing two blocks of four NF-κB -responsive sequences from the human JCV neurotropic polyoma virus promoter, fused to a new tight minimal CMV promoter, optimally distant from each other. A therapeutical gene, glial cell line-derived neurotrophic factor (GDNF) cDNA under the control of serotype 1-encapsidated NF-κB -responsive AAV vector (AAV-NF) was protective in senescent cultures of mouse cortical neurons. AAV-NF was then evaluated in vivo in the kainic acid (KA)-induced status epilepticus rat model for temporal lobe epilepsy, a major neurological disorder with a central pathophysiological role for NF-κB activation. We demonstrate that AAV-NF, injected in the hippocampus, responded to disease induction by mediating GFP expression, preferentially in CA1 and CA3 neurons and astrocytes, specifically in regions where inflammatory markers were also induced. Altogether, these data demonstrate the feasibility to use disease-activated transcription factor-responsive elements in order to drive transgene expression specifically in affected cells in inflammatory CNS disorders using AAV-mediated gene transfer.Abdelwahed ChtartoOlivier BockstaelElias GebaraKatia VermoesenCatherine MelasCatherine PythoudMarc LevivierOlivier De WitteRuth Luthi-CarterRalph ClinkersLiliane TenenbaumPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 1, p e53156 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Abdelwahed Chtarto
Olivier Bockstael
Elias Gebara
Katia Vermoesen
Catherine Melas
Catherine Pythoud
Marc Levivier
Olivier De Witte
Ruth Luthi-Carter
Ralph Clinkers
Liliane Tenenbaum
An adeno-associated virus-based intracellular sensor of pathological nuclear factor-κB activation for disease-inducible gene transfer.
description Stimulation of resident cells by NF-κB activating cytokines is a central element of inflammatory and degenerative disorders of the central nervous system (CNS). This disease-mediated NF-κB activation could be used to drive transgene expression selectively in affected cells, using adeno-associated virus (AAV)-mediated gene transfer. We have constructed a series of AAV vectors expressing GFP under the control of different promoters including NF-κB -responsive elements. As an initial screen, the vectors were tested in vitro in HEK-293T cells treated with TNF-α. The best profile of GFP induction was obtained with a promoter containing two blocks of four NF-κB -responsive sequences from the human JCV neurotropic polyoma virus promoter, fused to a new tight minimal CMV promoter, optimally distant from each other. A therapeutical gene, glial cell line-derived neurotrophic factor (GDNF) cDNA under the control of serotype 1-encapsidated NF-κB -responsive AAV vector (AAV-NF) was protective in senescent cultures of mouse cortical neurons. AAV-NF was then evaluated in vivo in the kainic acid (KA)-induced status epilepticus rat model for temporal lobe epilepsy, a major neurological disorder with a central pathophysiological role for NF-κB activation. We demonstrate that AAV-NF, injected in the hippocampus, responded to disease induction by mediating GFP expression, preferentially in CA1 and CA3 neurons and astrocytes, specifically in regions where inflammatory markers were also induced. Altogether, these data demonstrate the feasibility to use disease-activated transcription factor-responsive elements in order to drive transgene expression specifically in affected cells in inflammatory CNS disorders using AAV-mediated gene transfer.
format article
author Abdelwahed Chtarto
Olivier Bockstael
Elias Gebara
Katia Vermoesen
Catherine Melas
Catherine Pythoud
Marc Levivier
Olivier De Witte
Ruth Luthi-Carter
Ralph Clinkers
Liliane Tenenbaum
author_facet Abdelwahed Chtarto
Olivier Bockstael
Elias Gebara
Katia Vermoesen
Catherine Melas
Catherine Pythoud
Marc Levivier
Olivier De Witte
Ruth Luthi-Carter
Ralph Clinkers
Liliane Tenenbaum
author_sort Abdelwahed Chtarto
title An adeno-associated virus-based intracellular sensor of pathological nuclear factor-κB activation for disease-inducible gene transfer.
title_short An adeno-associated virus-based intracellular sensor of pathological nuclear factor-κB activation for disease-inducible gene transfer.
title_full An adeno-associated virus-based intracellular sensor of pathological nuclear factor-κB activation for disease-inducible gene transfer.
title_fullStr An adeno-associated virus-based intracellular sensor of pathological nuclear factor-κB activation for disease-inducible gene transfer.
title_full_unstemmed An adeno-associated virus-based intracellular sensor of pathological nuclear factor-κB activation for disease-inducible gene transfer.
title_sort adeno-associated virus-based intracellular sensor of pathological nuclear factor-κb activation for disease-inducible gene transfer.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/0f6019a6b6fb4efd9ffa751341864edc
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