A VSV-G Pseudotyped Last Generation Lentiviral Vector Mediates High Level and Persistent Gene Transfer in Models of Airway Epithelium In Vitro and In Vivo

Viruses

Elena Copreni¹  Lucia Palmieri¹  Stefano Castellani¹ 

[1] Institute for the Experimental Treatment of Cystic Fibrosis, H.S. Raffaele, via Olgettina 58, 20132 Milan, Italy; E-Mails: [e-mail] (E.C.); [e-mail] (L.P.); [e-mail] (S.C.)

关键词: lentivirus;    cystic fibrosis;    GFP;    luciferase;    lysophosphatidylcholine;    airway epithelial cells;    lung;    mice;   

DOI  :  10.3390/v2081577

来源: mdpi

【 摘 要 】

The aim of this work was to evaluate the efficiency and duration of gene expression mediated by a VSV-G pseudotyped last generation lentiviral (LV) vector. We studied LV efficiency in ex-vivo models of respiratory epithelial cells, obtained from bronchial biopsies and nasal polyps, by GFP epifluorescence and cytofluorimetry. In vivo efficiency and persistence of gene expression was investigated by GFP immunohistochemistry and luciferase activity in lung cryosections and homogenates, respectively, upon intranasal and intratracheal administration protocols in C57Bl/6 mice. Both primary bronchial and nasal epithelial cells were transduced up to 70-80% 72 hr after the LV infection. In vivo nasal luciferase expression was increased by lysophosphatidylcholine pre-treatment of the nose. Conversely, the bronchial epithelium was transduced in the absence of any pre-conditioning treatment and luciferase expression lasted for at least 6 months without any decline. We conclude that a last generation LV vector is a promising gene transfer agent in the target organ of genetic and acquired lung diseases, as in the case of cystic fibrosis.

【 授权许可】

CC BY   
© 2010 by the authors; licensee MDPI, Basel, Switzerland