Perfluorochemical liquid enhances adeno-associated virus-mediated transgene expression in lungs

被引:17
作者
Weiss, DJ
Bonneau, L
Allen, JM
Miller, AD
Halbert, CL
机构
[1] Fred Hutchinson Canc Res Ctr, Div Pulm & Crit Care Med, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98109 USA
关键词
adeno-associated virus; perfluorochemical liquid; gene transfer; lungs; alkaline phosphatase;
D O I
10.1006/mthe.2000.0207
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
Use of adeno-associated virus (AAV) vectors for lung gene therapy is limited, in part, by low levels of AAV-mediated transgene expression in lungs. Generally, less than 1% of total airway and alveolar epithelial cells express transgene activity following vector administration. A means of improving AAV vector delivery could potentially enhance AAV-mediated gene expression in lungs. We have previously demonstrated that use of perfluorochemical (PFC) liquids improved overall levels of adenovirus vector-mediated gene expression as well as distribution of expression in lungs of spontaneously breathing rodents. To evaluate whether use of PFC liquids might similarly enhance AAV-mediated expression, spontaneously breathing rodents received intratracheal instillation of the AAV vectors CWRAP and ARAP4 (2-5 x 10(8) FFU/animal) with or without 10 cc/kg body wt PFC liquid (FC-75, ACROS). Animals were sacrificed 4 weeks later and lungs assessed for overall and in situ alkaline phosphatase (AP) expression. Animals receiving vector alone exhibited scattered sparse in situ activity, predominantly in alveolar epithelium. In contrast, animals receiving vector with FC-75 exhibited increased and more widespread AP expression as well as up to a 26-fold increase in AP activity. These results demonstrate that use of the PFC liquid FC-75 improves overall and in situ AAV-mediated gene expression in rodent lungs.
引用
收藏
页码:624 / 630
页数:7
相关论文
共 29 条
[1]   Improved adeno-associated virus vector production with transfection of a single helper adenovirus gene, E4orf6 [J].
Allen, JM ;
Halbert, CL ;
Miller, AD .
MOLECULAR THERAPY, 2000, 1 (01) :88-95
[2]   Infectious entry pathway of adeno-associated virus and adeno-associated virus vectors [J].
Bartlett, JS ;
Wilcher, R ;
Samulski, RJ .
JOURNAL OF VIROLOGY, 2000, 74 (06) :2777-2785
[3]  
Bonneau L., 2000, AM J RESP CRIT CARE, V161, pA902
[4]   SURVIVAL OF MAMMALS BREATHING ORGANIC LIQUIDS EQUILIBRATED WITH OXYGEN AT ATMOSPHERIC PRESSURE [J].
CLARK, LC ;
GOLLAN, F .
SCIENCE, 1966, 152 (3730) :1755-&
[5]  
Conrad CK, 1996, GENE THER, V3, P658
[6]   Polarity influences the efficiency of recombinant adenoassociated virus infection in differentiated airway epithelia [J].
Duan, DS ;
Yue, YP ;
Yan, ZY ;
McCray, PB ;
Engelhardt, JF .
HUMAN GENE THERAPY, 1998, 9 (18) :2761-2776
[7]   Integration of adeno-associated virus vectors in CD34(+) human hematopoietic progenitor cells after transduction [J].
FisherAdams, G ;
Wong, KK ;
Podsakoff, G ;
Forman, SJ ;
Chatterjee, S .
BLOOD, 1996, 88 (02) :492-504
[8]   STABLE IN-VIVO EXPRESSION OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR WITH AN ADENOASSOCIATED VIRUS VECTOR [J].
FLOTTE, TR ;
AFIONE, SA ;
CONRAD, C ;
MCGRATH, SA ;
SOLOW, R ;
OKA, H ;
ZEITLIN, PL ;
GUGGINO, WB ;
CARTER, BJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (22) :10613-10617
[9]   A fluorescence video-endoscopy technique for detection of gene transfer and expression [J].
Flotte, TR ;
Beck, SE ;
Chesnut, K ;
Potter, M ;
Poirier, A ;
Zolotukhin, S .
GENE THERAPY, 1998, 5 (02) :166-173
[10]   Transduction by adeno-associated virus vectors in the rabbit airway: Efficiency, persistence, and readministration [J].
Halbert, CL ;
Standaert, TA ;
Aitken, ML ;
Alexander, IE ;
Russell, DW ;
Miller, AD .
JOURNAL OF VIROLOGY, 1997, 71 (08) :5932-5941