SITE-SPECIFIC GENE-EXPRESSION INVIVO BY DIRECT GENE-TRANSFER INTO THE ARTERIAL-WALL

被引:506
作者
NABEL, EG [1 ]
PLAUTZ, G [1 ]
NABEL, GJ [1 ]
机构
[1] UNIV MICHIGAN,MED CTR,HOWARD HUGHES MED INST,DEPT BIOL CHEM,ANN ARBOR,MI 48109
关键词
D O I
10.1126/science.2119055
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A recombinant β-galactosidase gene has been expressed in a specific arterial segment in vivo by direct infection with a murine amphotropic retroviral vector or by DNA transfection with the use of liposomes. Several cell types in the vessel wall were transduced, including endothelial and vascular smooth muscle cells. After retroviral infection, a recombinant reporter gene was expressed for at least 5 months, and no helper virus was detected. Recombinant gene expression achieved by direct retroviral infection or liposome-mediated DNA transfection was limited to the site of infection and was absent from liver, lung, kidney, and spleen. These results demonstrate that site-specific gene expression can be achieved by direct gene transfer in vivo and could be applied to the treatment of such human diseases as atherosclerosis or cancer.
引用
收藏
页码:1285 / 1288
页数:4
相关论文
共 22 条
[1]   HIGH-EFFICIENCY GENE-TRANSFER INTO MAMMALIAN-CELLS - GENERATION OF HELPER-FREE RECOMBINANT RETROVIRUS WITH BROAD MAMMALIAN HOST RANGE [J].
CONE, RD ;
MULLIGAN, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (20) :6349-6353
[2]  
DANNENBERG AM, 1981, METHODS STUDYING MON, P375
[3]   SAFE AND EFFICIENT GENERATION OF RECOMBINANT RETROVIRUSES WITH AMPHOTROPIC AND ECOTROPIC HOST RANGES [J].
DANOS, O ;
MULLIGAN, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (17) :6460-6464
[4]   SEEDING OF INTRAVASCULAR STENTS WITH GENETICALLY ENGINEERED ENDOTHELIAL-CELLS [J].
DICHEK, DA ;
NEVILLE, RF ;
ZWIEBEL, JA ;
FREEMAN, SM ;
LEON, MB ;
ANDERSON, WF .
CIRCULATION, 1989, 80 (05) :1347-1353
[5]   RESTENOSIS FOLLOWING TRANS-LUMINAL ANGIOPLASTY IN EXPERIMENTAL ATHEROSCLEROSIS [J].
FAXON, DP ;
SANBORN, TA ;
WEBER, VJ ;
HAUDENSCHILD, C ;
GOTTSMAN, SB ;
MCGOVERN, WA ;
RYAN, TJ .
ARTERIOSCLEROSIS, 1984, 4 (03) :189-195
[6]   INTERLEUKIN-2 PRODUCTION BY TUMOR-CELLS BYPASSES T-HELPER FUNCTION IN THE GENERATION OF AN ANTITUMOR RESPONSE [J].
FEARON, ER ;
PARDOLL, DM ;
ITAYA, T ;
GOLUMBEK, P ;
LEVITSKY, HI ;
SIMONS, JW ;
KARASUYAMA, H ;
VOGELSTEIN, B ;
FROST, P .
CELL, 1990, 60 (03) :397-403
[7]   TYPE-I MACROPHAGE SCAVENGER RECEPTOR CONTAINS ALPHA-HELICAL AND COLLAGEN-LIKE COILED COILS [J].
KODAMA, T ;
FREEMAN, M ;
ROHRER, L ;
ZABRECKY, J ;
MATSUDAIRA, P ;
KRIEGER, M .
NATURE, 1990, 343 (6258) :531-535
[8]   CONSTRUCTION OF A RETROVIRUS PACKAGING MUTANT AND ITS USE TO PRODUCE HELPER-FREE DEFECTIVE RETROVIRUS [J].
MANN, R ;
MULLIGAN, RC ;
BALTIMORE, D .
CELL, 1983, 33 (01) :153-159
[9]  
MAYER RJ, 1987, IMMUNOCHEMICAL METHO, P263
[10]   RESTENOSIS AFTER SUCCESSFUL CORONARY ANGIOPLASTY - PATHO-PHYSIOLOGY AND PREVENTION [J].
MCBRIDE, W ;
LANGE, RA ;
HILLIS, LD .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (26) :1734-1737