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In vivo genetic manipulation of inner ear connexin expression by bovine adeno-associated viral vectors

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Veröffentlicht in: Scientific reports 7(2017) Artikel-Nummer 6567, 13 Seiten
Personen und Körperschaften: Crispino, Giulia (VerfasserIn), Praetorius, Mark (VerfasserIn)
Titel: In vivo genetic manipulation of inner ear connexin expression by bovine adeno-associated viral vectors/ Giulia Crispino, Fabian Galindo Ramirez, Matteo Campioni, Veronica Zorzi, Mark Praetorius, Giovanni Di Pasquale, John A. Chiorini, Fabio Mammano
Format: E-Book-Kapitel
Sprache: Englisch
veröffentlicht:
04 August 2017
Gesamtaufnahme: : Scientific reports, 7(2017) Artikel-Nummer 6567, 13 Seiten
, volume:7
Quelle: Verbunddaten SWB
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Zusammenfassung: We have previously shown that in vitro transduction with bovine adeno-associated viral (BAAV) vectors restores connexin expression and rescues gap junction coupling in cochlear organotypic cultures from connexin-deficient mice that are models DFNB1 nonsyndromic hearing loss and deafness. The aims of this study were to manipulate inner ear connexin expression in vivo using BAAV vectors, and to identify the optimal route of vector delivery. Injection of a BAAV vector encoding a bacterial Cre recombinase via canalostomy in adult mice with floxed connexin 26 (Cx26) alleles promoted Cre/LoxP recombination, resulting in decreased Cx26 expression, decreased endocochlear potential, increased hearing thresholds, and extensive loss of outer hair cells. Injection of a BAAV vector encoding GFP-tagged Cx30 via canalostomy in P4 mice lacking connexin 30 (Cx30) promoted formation of Cx30 gap junctions at points of contacts between adjacent non-sensory cells of the cochlear sensory epithelium. Levels of exogenous Cx30 decayed over time, but were still detectable four weeks after canalostomy. Our results suggest that persistence of BAAV-mediated gene replacement in the cochlea is limited by the extensive remodeling of the organ of Corti throughout postnatal development and associated loss of non-sensory cells.
Beschreibung: Gesehen am 03.04.2018
Umfang: 13
ISSN: 2045-2322
DOI: 10.1038/s41598-017-06759-y