A single intravenous AAV9 injection mediates bilateral gene transfer to the adult mouse retina.

Widespread gene delivery to the retina is an important challenge for the treatment of retinal diseases, such as retinal dystrophies. We and others have recently shown that the intravenous injection of a self-complementary (sc) AAV9 vector can direct efficient cell transduction in the central nervous...

Full description

Bibliographic Details
Main Authors: Alexis-Pierre Bemelmans, Sandra Duqué, Christel Rivière, Stéphanie Astord, Mélissa Desrosiers, Thibault Marais, José-Alain Sahel, Thomas Voit, Martine Barkats
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3626698?pdf=render
_version_ 1811264670257905664
author Alexis-Pierre Bemelmans
Sandra Duqué
Christel Rivière
Stéphanie Astord
Mélissa Desrosiers
Thibault Marais
José-Alain Sahel
Thomas Voit
Martine Barkats
author_facet Alexis-Pierre Bemelmans
Sandra Duqué
Christel Rivière
Stéphanie Astord
Mélissa Desrosiers
Thibault Marais
José-Alain Sahel
Thomas Voit
Martine Barkats
author_sort Alexis-Pierre Bemelmans
collection DOAJ
description Widespread gene delivery to the retina is an important challenge for the treatment of retinal diseases, such as retinal dystrophies. We and others have recently shown that the intravenous injection of a self-complementary (sc) AAV9 vector can direct efficient cell transduction in the central nervous system, in both neonatal and adult animals. We show here that the intravenous injection of scAAV9 encoding green fluorescent protein (GFP) resulted in gene transfer to all layers of the retina in adult mice, despite the presence of a mature blood-eye barrier. Cell morphology studies and double-labeling with retinal cell-specific markers showed that GFP was expressed in retinal pigment epithelium cells, photoreceptors, bipolar cells, Müller cells and retinal ganglion cells. The cells on the inner side of the retina, including retinal ganglion cells in particular, were transduced with the highest efficiency. Quantification of the cell population co-expressing GFP and Brn-3a showed that 45% of the retinal ganglion cells were efficiently transduced after intravenous scAAV9-GFP injection in adult mice. This study provides the first demonstration that a single intravenous scAAV9 injection can deliver transgenes to the retinas of both eyes in adult mice, suggesting that this vector serotype is able to cross mature blood-eye barriers. This intravascular gene transfer approach, by eliminating the potential invasiveness of ocular surgery, could constitute an alternative when fragility of the retina precludes subretinal or intravitreal injections of viral vectors, opening up new possibilities for gene therapy for retinal diseases.
first_indexed 2024-04-12T20:08:32Z
format Article
id doaj.art-e048910f81a046eda072ae57275f1bdd
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-04-12T20:08:32Z
publishDate 2013-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-e048910f81a046eda072ae57275f1bdd2022-12-22T03:18:20ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0184e6161810.1371/journal.pone.0061618A single intravenous AAV9 injection mediates bilateral gene transfer to the adult mouse retina.Alexis-Pierre BemelmansSandra DuquéChristel RivièreStéphanie AstordMélissa DesrosiersThibault MaraisJosé-Alain SahelThomas VoitMartine BarkatsWidespread gene delivery to the retina is an important challenge for the treatment of retinal diseases, such as retinal dystrophies. We and others have recently shown that the intravenous injection of a self-complementary (sc) AAV9 vector can direct efficient cell transduction in the central nervous system, in both neonatal and adult animals. We show here that the intravenous injection of scAAV9 encoding green fluorescent protein (GFP) resulted in gene transfer to all layers of the retina in adult mice, despite the presence of a mature blood-eye barrier. Cell morphology studies and double-labeling with retinal cell-specific markers showed that GFP was expressed in retinal pigment epithelium cells, photoreceptors, bipolar cells, Müller cells and retinal ganglion cells. The cells on the inner side of the retina, including retinal ganglion cells in particular, were transduced with the highest efficiency. Quantification of the cell population co-expressing GFP and Brn-3a showed that 45% of the retinal ganglion cells were efficiently transduced after intravenous scAAV9-GFP injection in adult mice. This study provides the first demonstration that a single intravenous scAAV9 injection can deliver transgenes to the retinas of both eyes in adult mice, suggesting that this vector serotype is able to cross mature blood-eye barriers. This intravascular gene transfer approach, by eliminating the potential invasiveness of ocular surgery, could constitute an alternative when fragility of the retina precludes subretinal or intravitreal injections of viral vectors, opening up new possibilities for gene therapy for retinal diseases.http://europepmc.org/articles/PMC3626698?pdf=render
spellingShingle Alexis-Pierre Bemelmans
Sandra Duqué
Christel Rivière
Stéphanie Astord
Mélissa Desrosiers
Thibault Marais
José-Alain Sahel
Thomas Voit
Martine Barkats
A single intravenous AAV9 injection mediates bilateral gene transfer to the adult mouse retina.
PLoS ONE
title A single intravenous AAV9 injection mediates bilateral gene transfer to the adult mouse retina.
title_full A single intravenous AAV9 injection mediates bilateral gene transfer to the adult mouse retina.
title_fullStr A single intravenous AAV9 injection mediates bilateral gene transfer to the adult mouse retina.
title_full_unstemmed A single intravenous AAV9 injection mediates bilateral gene transfer to the adult mouse retina.
title_short A single intravenous AAV9 injection mediates bilateral gene transfer to the adult mouse retina.
title_sort single intravenous aav9 injection mediates bilateral gene transfer to the adult mouse retina
url http://europepmc.org/articles/PMC3626698?pdf=render
work_keys_str_mv AT alexispierrebemelmans asingleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT sandraduque asingleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT christelriviere asingleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT stephanieastord asingleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT melissadesrosiers asingleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT thibaultmarais asingleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT josealainsahel asingleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT thomasvoit asingleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT martinebarkats asingleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT alexispierrebemelmans singleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT sandraduque singleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT christelriviere singleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT stephanieastord singleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT melissadesrosiers singleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT thibaultmarais singleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT josealainsahel singleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT thomasvoit singleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina
AT martinebarkats singleintravenousaav9injectionmediatesbilateralgenetransfertotheadultmouseretina