Transfection efficiency and toxicity following delivery of naked plasmid DNA and cationic lipid-DNA complexes to ovine lung segments

被引:28
作者
Emerson, M
Renwick, L
Tate, S
Rhind, S
Milne, E
Painter, H
Boyd, AC
McLachlan, G
Griesenbach, U
Cheng, SH
Gill, DR
Hyde, SC
Baker, A
Alton, EW
Porteous, DJ
Collie, DDS
机构
[1] Univ Edinburgh, Coll Med & Vet Med, Med Genet Sect, Sch Mol & Clin Med, Edinburgh EH8 9AG, Midlothian, Scotland
[2] Univ Edinburgh, Coll Med & Vet Med, Dept Vet Pathol, Edinburgh EH8 9AG, Midlothian, Scotland
[3] Univ Edinburgh, Coll Med & Vet Med, Dept Vet Clin Studies, Edinburgh EH8 9AG, Midlothian, Scotland
[4] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Lab Sci, Gene Med Grp, Oxford OX3 9DU, England
[5] Univ London Imperial Coll Sci Technol & Med, Fac Med, Dept Gene Therapy, London SW3 6LR, England
基金
英国医学研究理事会;
关键词
cationic lipid; gene transfer; lung; toxicology; chloramphenicol acetyltransferase; RNA; messenger; sheep; domestic; genetic vectors; cystic fibrosis;
D O I
10.1016/S1525-0016(03)00233-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We defined, using a novel large animal model system, the acute pathologic response to localized pulmonary administration of either naked plasmid DNA (pDNA) or cationic lipid-pDNA complexes (pDNA:GL67) and related such responses to concomitant indicators of transfection efficiency, namely levels of chloramphenicol acetyl transferase (CAT) protein and mRNA in specific lung tissue compartments. We instilled doses of 0.2, 1, and 5 mg pDNA to spatially distinct lung segments in six anesthetized sheep and doses of 0.2, 1, and 5 mg pDNA:GL67 to a further six sheep. Twenty-four hours after gene delivery the sheep were euthanized and necropsy examination with sampling of relevant tissues was carried out. Levels of plasmid-derived CAT-specific mRNA and CAT protein in samples derived from segments treated with either pDNA or pDNA: GL67 increased in relation to the administered dose. Levels of mRNA and protein expression were greater for pDNA:GL67 than for pDNA alone. A significant correlation was observed between mRNA and protein expression in samples derived from airways treated with pDNA:GL67. Histopathological changes following administration of both pDNA and pDNA:GL67 were characterized by a neutrophilic inflammation predominantly oriented on airways. The severity of the inflammatory response appeared to correlate with the administered dose of DNA and was generally more severe for pDNA:GL67.
引用
收藏
页码:646 / 653
页数:8
相关论文
共 28 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]  
BICE D E, 1989, Regional Immunology, V2, P376
[3]   AN ULTRASTRUCTURAL-STUDY OF PULMONARY BRONCHIOLAR AND ALVEOLAR EPITHELIUM IN SHEEP [J].
BOULJIHAD, M ;
LEIPOLD, HW .
JOURNAL OF VETERINARY MEDICINE SERIES A-ZENTRALBLATT FUR VETERINARMEDIZIN REIHE A-PHYSIOLOGY PATHOLOGY CLINICAL MEDICINE, 1994, 41 (08) :573-586
[4]   Sheep cloned by nuclear transfer from a cultured cell line [J].
Campbell, KHS ;
McWhir, J ;
Ritchie, WA ;
Wilmut, I .
NATURE, 1996, 380 (6569) :64-66
[5]   Local lung responses following local lung challenge with recombinant lungworm antigen in systemically sensitized sheep [J].
Collie, DDS ;
MacAldowie, CN ;
Pemberton, AD ;
Woodall, CJ ;
McLean, N ;
Hodgson, C ;
Kennedy, MW ;
Miller, HRP .
CLINICAL AND EXPERIMENTAL ALLERGY, 2001, 31 (10) :1636-1647
[6]   Evaluation of a porcine model for pulmonary gene transfer using a novel synthetic vector [J].
Cunningham, S ;
Meng, QH ;
Klein, N ;
McAnulty, RJ ;
Hart, SL .
JOURNAL OF GENE MEDICINE, 2002, 4 (04) :438-446
[7]   A concentrated and stable aerosol formulation of cationic Lipid: DNA complexes giving high-level gene expression in mouse lung [J].
Eastman, SJ ;
Lukason, MJ ;
Tousignant, JD ;
Murray, H ;
Lane, MD ;
StGeorge, JA ;
Akita, GY ;
Cherry, M ;
Cheng, SH ;
Scheule, RK .
HUMAN GENE THERAPY, 1997, 8 (06) :765-773
[8]   Local release of eosinophil peroxidase following segmental allergen provocation in asthma [J].
Erpenbeck, VJ ;
Hohlfeld, JM ;
Petschallies, J ;
Eklund, E ;
Peterson, CGB ;
Fabel, H ;
Krug, N .
CLINICAL AND EXPERIMENTAL ALLERGY, 2003, 33 (03) :331-336
[9]   Mucus altering agents as adjuncts for nonviral gene transfer to airway epithelium [J].
Ferrari, S ;
Kitson, C ;
Farley, R ;
Steel, R ;
Marriott, C ;
Parkins, DA ;
Scarpa, M ;
Wainwright, B ;
Evans, MJ ;
Colledge, WH ;
Geddes, DM ;
Alton, EWFW .
GENE THERAPY, 2001, 8 (18) :1380-1386
[10]   ALTERED ADHESION MOLECULE EXPRESSION AND ENDOTHELIAL-CELL ACTIVATION ACCOMPANY THE RECRUITMENT OF HUMAN GRANULOCYTES TO THE LUNG AFTER SEGMENTAL ANTIGEN CHALLENGE [J].
GEORAS, SN ;
LIU, MC ;
NEWMAN, W ;
BEALL, LD ;
STEALEY, BA ;
BOCHNER, BS .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 7 (03) :261-269