The use of carboxymethylcellulose gel to increase non-viral gene transfer in mouse airways

Uta Griesenbach, Cuixiang Meng, Raymond Farley, Marguerite Y. Wasowicz, Felix M. Munkonge, Mario Chan, Charlotte Stoneham, Stephanie G. Sumner-Jones, Ian A. Pringle, Deborah R. Gill, Stephen C. Hyde, Barbara Stevenson, Emma Holder, Hiroshi Ban, Mamoru Hasegawa, Seng H. Cheng, Ronald K. Scheule, Patrick L. Sinn, Paul B. McCray, Eric W. F. W. Alton

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

We have assessed whether viscoelastic gels known to inhibit mucociliary clearance call increase lipid-mediated gene transfer. Methylcellulose or carboxymethylcellulose (025-1.5%) was mixed with complexes of the cationic lipid GL67A and plasmids encoding luciferase and perfused onto the nasal epithelium Of mice Survival after perfusion with 1% CMC or 1% MC was 90 and 100%. respectively In contrast 15% CMC was uniformly lethal likely due to the VISCOUS Solution blocking the airways Perfusion with 0 5% CMC containing lipid/DNA complexes reproducibly increased gene expression by approximately 3-fold (n = 16. p < 0 05) Given this benefit, likely related to increased duration of contact, we also assessed the effect of prolonging contact time of the liposome/DNA complexes by delivering our standard 80 jig DNA close over either approximately 22 or 60 min of perfusion This independently increased gene transfer by 6-fold (n = 8, p < 0 05) and Could be further enhanced by the addition of 0 5% CMC, leading to an overall 25-fold enhancement (n = 5. p < 0 001) in gene expression As a result of these interventions CFTR transgene mRNA transgene levels were increased several logs above background Interestingly, this did not lead to correction of the ion transport defects in the nasal epithelium of cystic fibrosis mice nor for immunohistochemical quantification of CFTR expression. To assess if 0 5% CMC also increased gene transfer in the mouse lung, we used whole body nebulisation chambers CMC was nebulised for 1 h immediately before, or simultaneously with GL67A/pCIKLux The former did not increase gene transfer. whereas co-administration significantly increased gene transfer by 4-fold (p < 0 0001. n = 18) This study Suggests that contact little of non-viral gene transfer agents is a key factor for gene delivery, and suggests two methods which may be translatable for use in man (C) 2009 Elsevier Ltd All rights reserved

Original languageEnglish
Pages (from-to)2665-2672
Number of pages8
JournalBiomaterials
Volume31
Issue number9
DOIs
Publication statusPublished - Mar 2010

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