PRIOR ARTERIAL INJURY ENHANCES LUCIFERASE EXPRESSION FOLLOWING INVIVO GENE-TRANSFER

被引:16
作者
BARBEE, RW
STAPLETON, DD
PERRY, BD
RE, RN
MURGO, JP
VALENTINO, VA
COOK, JL
机构
[1] ALTON OCHSNER MED INST, DEPT INTERNAL MED, DIV RES, NEW ORLEANS, LA 70121 USA
[2] ALTON OCHSNER MED INST, DEPT INTERNAL MED, CARDIOL SECT, NEW ORLEANS, LA 70121 USA
关键词
D O I
10.1006/bbrc.1993.1012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We determined the time course of gene expression following DNA/Lipofectin transfection of normal or previously injured arterial segments using direct intraluminal infusion following surgical exposure. Constructs possessing the firefly luciferase cDNA regulated by Simian virus 40, Rous sarcoma virus, or α-actin promoter were incubated together with Lipofectin for 30 minutes. Arterial segments were assayed for luciferase activity following harvest at 2-21 days. Without prior injury, luciferase activity was only 2.5-fold greater than background two days following gene transfer. Arterial injury three days before gene transfer resulted in luciferase activity 12.5-fold over background levels. This observation has clinical implications with regard to gene therapy following angioplasty, a procedure that is associated with endothelial cell denudation and smooth muscle cell proliferation. Maintenance of gene expression for several days could ameliorate the early smooth muscle migration and proliferation following arterial injury. © 1993 Academic Press, Inc.
引用
收藏
页码:70 / 78
页数:9
相关论文
共 37 条
[1]   REPORTER GENES - APPLICATION TO THE STUDY OF MAMMALIAN GENE-TRANSCRIPTION [J].
ALAM, J ;
COOK, JL .
ANALYTICAL BIOCHEMISTRY, 1990, 188 (02) :245-254
[2]   2-DIMENSIONAL IN-VITRO STUDIES OF FEMORAL ARTERIAL WALLS OF DOG [J].
ATTINGER, FM .
CIRCULATION RESEARCH, 1968, 22 (06) :829-&
[3]   RABBIT EAR MODEL OF INJURY-INDUCED ARTERIAL SMOOTH-MUSCLE CELL-PROLIFERATION - KINETICS, REPRODUCIBILITY, AND IMPLICATIONS [J].
BANAI, S ;
SHOU, M ;
CORREA, R ;
JAKLITSCH, MT ;
DOUEK, PC ;
BONNER, RF ;
EPSTEIN, SE ;
UNGER, EF .
CIRCULATION RESEARCH, 1991, 69 (03) :748-756
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]  
BRASIER AR, 1989, BIOTECHNIQUES, V7, P1116
[6]  
CAMPBELL GR, 1988, ARCH PATHOL LAB MED, V112, P977
[7]   GENE-TRANSFER INTO CORONARY-ARTERIES OF INTACT ANIMALS WITH A PERCUTANEOUS BALLOON CATHETER [J].
CHAPMAN, GD ;
LIM, CS ;
GAMMON, RS ;
CULP, SC ;
DESPER, JS ;
BAUMAN, RP ;
SWAIN, JL ;
STACK, RS .
CIRCULATION RESEARCH, 1992, 71 (01) :27-33
[8]   SIGNIFICANCE OF QUIESCENT SMOOTH-MUSCLE MIGRATION IN THE INJURED RAT CAROTID-ARTERY [J].
CLOWES, AW ;
SCHWARTZ, SM .
CIRCULATION RESEARCH, 1985, 56 (01) :139-145
[9]  
DELUCA M, 1978, METHOD ENZYMOL, V57, P7
[10]   PERCUTANEOUS TRANS-LUMINAL CORONARY ANGIOPLASTY IN 1985-1986 AND 1977-1981 - THE NATIONAL-HEART-LUNG-AND-BLOOD-INSTITUTE REGISTRY [J].
DETRE, K ;
HOLUBKOV, R ;
KELSEY, S ;
COWLEY, M ;
KENT, K ;
WILLIAMS, D ;
MYLER, R ;
FAXON, D ;
HOLMES, D ;
BOURASSA, M ;
BLOCK, P ;
GOSSELIN, A ;
BENTIVOGLIO, L ;
LEATHERMAN, L ;
DORROS, G ;
KING, S ;
GALICHIA, J ;
ALBASSAM, M ;
LEON, M ;
ROBERTSON, T ;
PASSAMANI, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (05) :265-270