Tyrosine Mutation in AAV9 Capsid Improves Gene Transfer to the Mouse Lung.
Cell Physiol Biochem
; 39(2): 544-53, 2016.
Article
en En
| MEDLINE
| ID: mdl-27384068
ABSTRACT
BACKGROUND/AIMS:
Adeno-associated virus (AAV) vectors are being increasingly used as the vector of choice for in vivo gene delivery and gene therapy for many pulmonary diseases. Recently, it was shown that phosphorylation of surface-exposed tyrosine residues from AAV capsid targets the viral particles for ubiquitination and proteasome-mediated degradation, and mutations of these tyrosine residues lead to highly efficient vector transduction in vitro and in vivo in different organs. In this study, we evaluated the pulmonary transgene expression efficacy of AAV9 vectors containing point mutations in surface-exposed capsid tyrosine residues.METHODS:
Eighteen C57BL/6 mice were randomly assigned into three groups (1) a control group (CTRL) animals underwent intratracheal (i.t.) instillation of saline, (2) the wild-type AAV9 group (WT-AAV9, 1010 vg), and (3) the tyrosine-mutant Y731F AAV9 group (M-AAV9, 1010 vg), which received (i.t.) self-complementary AAV9 vectors containing the DNA sequence of enhanced green fluorescence protein (eGFP). Four weeks after instillation, lung mechanics, morphometry, tissue cellularity, gene expression, inflammatory cytokines, and growth factor expression were analyzed.RESULTS:
No significant differences were observed in lung mechanics and morphometry among the experimental groups. However, the number of polymorphonuclear cells was higher in the WT-AAV9 group than in the CTRL and M-AAV9 groups, suggesting that the administration of tyrosine-mutant AAV9 vectors was better tolerated. Tyrosine-mutant AAV9 vectors significantly improved transgene delivery to the lung (30%) compared with their wild-type counterparts, without eliciting an inflammatory response.CONCLUSION:
Our results provide the impetus for further studies to exploit the use of AAV9 vectors as a tool for pulmonary gene therapy.
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Bases de datos:
MEDLINE
Asunto principal:
Tirosina
/
Transfección
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Mutación Puntual
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Dependovirus
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Proteínas de la Cápside
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Pulmón
Idioma:
En
Revista:
Cell Physiol Biochem
Año:
2016
Tipo del documento:
Article
País de afiliación:
Brasil