PLASMID DNA IS SUPERIOR TO VIRAL VECTORS FOR DIRECT GENE-TRANSFER INTO ADULT-MOUSE SKELETAL-MUSCLE

被引:268
作者
DAVIS, HL
DEMENEIX, BA
QUANTIN, B
COULOMBE, J
WHALEN, RG
机构
[1] UNIV OTTAWA,FAC MED,DEPT PHYSIOL,OTTAWA K1H 8M5,ONTARIO,CANADA
[2] UNIV OTTAWA,FAC MED,DEPT BIOCHEM,OTTAWA K1H 8M5,ONTARIO,CANADA
[3] MUSEUM NATL HIST NAT,PHYSIOL GEN & COMPAREE LAB,F-75231 PARIS 05,FRANCE
[4] INST CHIM BIOL,GEN MOLEC EUCARYOTES LAB,CNRS,INSERM,U184,F-67085 STRASBOURG,FRANCE
[5] INST PASTEUR,DEPT BIOL MOLEC,F-75724 PARIS 15,FRANCE
关键词
D O I
10.1089/hum.1993.4.6-733
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
Direct gene transfer into skeletal muscle offers several therapeutic possibilities. We assessed direct intramuscular injection of recombinant plasmids, adenovirus, or retrovirus in normal or regenerating muscles of mice. The incorporation and expression of reporter genes introduced by any of these three vectors is greater in regenerating than in mature muscle. In regenerating muscle, pure DNA and adenovirus result in equivalent numbers of fibers expressing reporter gene (>10%), but adenovirus also induces considerable cellular infiltration. In mature muscle, recombinant DNA is better than adenovirus. Retrovirus failed to infect mature muscle fibers and was less effective than plasmid DNA or adenovirus in regenerating muscle. The surprisingly high relative efficiency of pure plasmid DNA suggests that this method will provide a simple, safe and viable alternative for gene therapy involving muscle tissue.
引用
收藏
页码:733 / 740
页数:8
相关论文
共 41 条
  • [1] ACSADI G, 1991, NEW BIOL, V3, P71
  • [2] SYSTEMIC DELIVERY OF RECOMBINANT PROTEINS BY GENETICALLY MODIFIED MYOBLASTS
    BARR, E
    LEIDEN, JM
    [J]. SCIENCE, 1991, 254 (5037) : 1507 - 1509
  • [3] BENOIT PW, 1970, J ANAT, V107, P547
  • [4] BUTLERBROWNE GS, 1987, J BIOL CHEM, V262, P15188
  • [5] GENE-THERAPY VIA PRIMARY MYOBLASTS - LONG-TERM EXPRESSION OF FACTOR-IX PROTEIN FOLLOWING TRANSPLANTATION INVIVO
    DAI, Y
    ROMAN, M
    NAVIAUX, RK
    VERMA, IM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (22) : 10892 - 10895
  • [6] MYOSIN ISOFORM TRANSITIONS IN REGENERATION OF FAST AND SLOW MUSCLES DURING POSTNATAL-DEVELOPMENT OF THE RAT
    DALBIS, A
    COUTEAUX, R
    JANMOT, C
    MIRA, JC
    [J]. DEVELOPMENTAL BIOLOGY, 1989, 135 (02) : 320 - 325
  • [7] DANNENBERG AM, 1981, METHODS STUDYING MON, P375
  • [8] DNA-BASED IMMUNIZATION INDUCES CONTINUOUS SECRETION OF HEPATITIS-B SURFACE-ANTIGEN AND HIGH-LEVELS OF CIRCULATING ANTIBODY
    DAVIS, HL
    MICHEL, ML
    WHALEN, RG
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (11) : 1847 - 1851
  • [9] DIRECT GENE-TRANSFER INTO SKELETAL-MUSCLE INVIVO - FACTORS AFFECTING EFFICIENCY OF TRANSFER AND STABILITY OF EXPRESSION
    DAVIS, HL
    WHALEN, RG
    DEMENEIX, BA
    [J]. HUMAN GENE THERAPY, 1993, 4 (02) : 151 - 159
  • [10] SYSTEMIC DELIVERY OF HUMAN GROWTH-HORMONE BY INJECTION OF GENETICALLY ENGINEERED MYOBLASTS
    DHAWAN, J
    PAN, LC
    PAVLATH, GK
    TRAVIS, MA
    LANCTOT, AM
    BLAU, HM
    [J]. SCIENCE, 1991, 254 (5037) : 1509 - 1512