Intraluminal water increases expression of plasmid DNA in rat lung

被引:25
作者
Sawa, T
Miyazaki, H
Pittet, JF
Widdicombe, JH
Gropper, MA
Hashimoto, S
Conrad, DJ
Folkesson, HG
Debs, R
Forsayeth, JR
Fox, B
WienerKronish, JP
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT ANESTHESIA & MED,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,CARDIOVASC RES INST,SAN FRANCISCO,CA 94143
[3] UNIV CALIF SAN FRANCISCO,DIV PULM & CRIT CARE,SAN FRANCISCO,CA 94143
[4] CALIF PACIFIC MED RES INST,SAN FRANCISCO,CA 94115
[5] KYOTO PREFECTURAL UNIV MED,DEPT ANESTHESIOL,DIV INTENS CARE UNIT,KYOTO 602,JAPAN
[6] MEGABIOS CORP,BURLINGAME,CA 94010
关键词
D O I
10.1089/hum.1996.7.8-933
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
Effective gene delivery to specific organs is a major goal for human gene therapy, The lung's structure allows instillation of agents into the airspaces, directly adjacent to the lung epithelium. We hypothesized that the airspace instillation of hypotonic solutions would increase the permeability of the lung epithelium and increase DNA uptake, This hypothesis was tested by instilling plasmid DNA (p4241) encoding the luciferase gene in isotonic and hypotonic solutions, The highest luciferase expression in the lung was achieved after the instillation of this plasmid DNA in distilled water, Aerosolization of water just before the instillation of the plasmid DNA also enhanced the expression level of luciferase in the lung, In addition, an intralobar instillation of the plasmid DNA in water significantly increased the luciferase expression, suggesting that the instillation of the plasmid over a smaller surface area increased expression, Levels of expression could be measured for 3 days, Water increases the permeability of lung epithelial cells transiently and/or enhances gene expression and can be used to achieve gene expression in the lung airspaces for short intervals without toxicity.
引用
收藏
页码:933 / 941
页数:9
相关论文
共 18 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]  
BUDELIER K, 1994, CURRENT PROTOCOLS MO
[3]   CHLORIDE SECRETION AND FUNCTION OF SEROUS AND MUCOUS CELLS OF HUMAN AIRWAY GLANDS [J].
FINKBEINER, WE ;
SHEN, BQ ;
WIDDICOMBE, JH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (02) :L206-L210
[4]   PERMEABILITY OF THE RESPIRATORY-TRACT TO DIFFERENT-SIZED MACROMOLECULES AFTER INTRATRACHEAL INSTILLATION IN YOUNG AND ADULT-RATS [J].
FOLKESSON, HG ;
WESTROM, BR ;
KARLSSON, BW .
ACTA PHYSIOLOGICA SCANDINAVICA, 1990, 139 (02) :347-354
[5]  
FORSAYETH JR, 1994, BIOTECHNIQUES, V17, P354
[6]   GENE-EXPRESSION FOLLOWING DIRECT-INJECTION OF DNA INTO LIVER [J].
HICKMAN, MA ;
MALONE, RW ;
LEHMANNBRUINSMA, K ;
SIH, TR ;
KNOELL, D ;
SZOKA, FC ;
WALZEM, R ;
CARLSON, DM ;
POWELL, JS .
HUMAN GENE THERAPY, 1994, 5 (12) :1477-1483
[7]   CATIONIC LIPOSOME-MEDIATED INTRAVENOUS GENE DELIVERY [J].
LIU, Y ;
LIGGITT, D ;
ZHONG, W ;
TU, GH ;
GAENSLER, K ;
DEBS, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) :24864-24870
[8]  
MEYER KB, 1995, GENE THER, V2, P450
[9]   PSEUDOMONAS-AERUGINOSA INDUCED LUNG AND PLEURAL INJURY IN SHEEP - DIFFERENTIAL PROTECTIVE EFFECT OF CIRCULATING VERSUS ALVEOLAR IMMUNOGLOBULIN-G ANTIBODY [J].
PITTET, JF ;
MATTHAY, MA ;
PIER, G ;
GRADY, M ;
WIENERKRONISH, JP .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (03) :1221-1228
[10]  
WIDDICOMBE JH, 1996, IN PRESS J APPL PHYS