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

被引:24
作者
Griesenbach, Uta [1 ]
Meng, Cuixiang [1 ]
Farley, Raymond [1 ]
Wasowicz, Marguerite Y. [1 ]
Munkonge, Felix M. [1 ]
Chan, Mario [1 ]
Stoneham, Charlotte [2 ]
Sumner-Jones, Stephanie G. [2 ]
Pringle, Ian A. [2 ]
Gill, Deborah R. [2 ]
Hyde, Stephen C. [2 ]
Stevenson, Barbara [3 ]
Holder, Emma [3 ]
Ban, Hiroshi [4 ]
Hasegawa, Mamoru [4 ]
Cheng, Seng H. [5 ]
Scheule, Ronald K. [5 ]
Sinn, Patrick L. [6 ]
McCray, Paul B., Jr. [6 ]
Alton, Eric W. F. W. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, Dept Gene Therapy, London SW3 6LR, England
[2] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Lab Sci, Oxford OX3 9DU, England
[3] Univ Edinburgh, Med Genet Sect, Edinburgh EH8 9YL, Midlothian, Scotland
[4] DNAVEC Corp, Tsukuba, Ibaraki, Japan
[5] Genzyme Corp, Framingham, MA 01701 USA
[6] Univ Iowa, Dept Pediat, Program Gene Therapy, Iowa City, IA 52242 USA
关键词
Gene transfer; Gene therapy; Lung; Epithelium; NASAL POTENTIAL DIFFERENCE; CYSTIC-FIBROSIS; CFTR GENE; IN-VIVO; EPITHELIUM; FORMULATIONS; EXPRESSION; PROTEIN; MODEL; MICE;
D O I
10.1016/j.biomaterials.2009.12.005
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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
引用
收藏
页码:2665 / 2672
页数:8
相关论文
共 31 条
[1]   Cationic lipid-mediated CFTR gene transfer to the lungs and nose of patients with cystic fibrosis:: a double-blind placebo-controlled trial [J].
Alton, EWFW ;
Stern, M ;
Farley, R ;
Jaffe, A ;
Chadwick, SL ;
Phillips, J ;
Davies, J ;
Smith, SN ;
Browning, J ;
Davies, MG ;
Hodson, ME ;
Durham, SR ;
Li, D ;
Jeffery, PK ;
Scallan, M ;
Balfour, R ;
Eastman, SJ ;
Cheng, SH ;
Smith, AE ;
Meeker, D ;
Geddes, DM .
LANCET, 1999, 353 (9157) :947-954
[2]   Expression and maturation of Sendai virus vector-derived CFTR protein: functional and biochemical evidence using a GFP-CFTR fusion protein [J].
Ban, H. ;
Inoue, M. ;
Griesenbach, U. ;
Munkonge, F. ;
Chan, M. ;
Iida, A. ;
Alton, Ewfw ;
Hasegawa, M. .
GENE THERAPY, 2007, 14 (24) :1688-1694
[3]   Comparative pharmacology of the activity of wild-type and G551D mutated CFTR chloride channel:: Effect of the benzimidazolone derivative NS004 [J].
Dérand, R ;
Bulteau-Pignoux, L ;
Becq, F .
JOURNAL OF MEMBRANE BIOLOGY, 2003, 194 (02) :109-117
[4]  
Dorfman R, 2009, CYSTIC FIBROSIS 21 C, P61
[5]   Sendai virus-mediated CFTR gene transfer to the airway epithelium [J].
Ferrari, S. ;
Griesenbach, U. ;
Iida, A. ;
Farley, R. ;
Wright, A. M. ;
Zhu, J. ;
Munkonge, F. M. ;
Smith, S. N. ;
You, J. ;
Ban, H. ;
Inoue, M. ;
Chan, M. ;
Singh, C. ;
Verdon, B. ;
Argent, B. E. ;
Wainwright, B. ;
Jeffery, P. K. ;
Geddes, D. M. ;
Porteous, D. J. ;
Hyde, S. C. ;
Gray, M. A. ;
Hasegawa, M. ;
Alton, E. W. F. W. .
GENE THERAPY, 2007, 14 (19) :1371-1379
[6]   The nasal epithelium as a factory for systemic protein delivery [J].
Griesenbach, U ;
Cassady, RL ;
Ferrari, S ;
Fukumura, M ;
Muller, C ;
Schmitt, E ;
Zhu, J ;
Jeffery, PK ;
Nagai, Y ;
Geddes, DM ;
Hasegawa, M ;
Alton, EWFW .
MOLECULAR THERAPY, 2002, 5 (02) :98-103
[7]  
GRIESENBACH U, 2009, AM J RESP CELL MOL B
[8]   Validation of nasal potential difference measurements in gut-corrected CF knockout mice [J].
Griesenbach, Uta ;
Smith, Stephen N. ;
Farley, Raymond ;
Singh, Charanjit ;
Alton, Eric W. F. W. .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2008, 39 (04) :490-496
[9]   Distribution, metabolism, and excretion of a novel surface-active agent, purified poloxamer 188, in rats, dogs, and humans [J].
Grindel, JM ;
Jaworski, T ;
Piraner, O ;
Emanuele, RM ;
Balasubramanian, M .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (09) :1936-1947
[10]   Ion transport across CF and normal murine olfactory and ciliated epithelium [J].
Grubb, B. R. ;
Rogers, T. D. ;
Boucher, R. C. ;
Ostrowski, L. E. .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2009, 296 (06) :C1301-C1309