Expression of adenovirus-mediated E-coli lacZ gene in skeletal muscles and spinal motor neurons of transgenic mice with a mutant superoxide dismutase gene

被引:11
作者
Warita, H
Abe, K
Setoguchi, Y
Itoyama, Y
机构
[1] Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 980, Japan
[2] Juntendo Univ, Sch Med, Dept Resp Med, Tokyo 113, Japan
关键词
gene transfer; lacZ gene; familial amyotrophic lateral sclerosis; superoxide dismutase; transgenic mouse;
D O I
10.1016/S0304-3940(98)00245-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A replication-defective recombinant adenoviral vector containing E. coli lacZ gene was injected into the right biceps brachii muscles of transgenic mice carrying mutant human Cu/Zn superoxide dismutase (SOD1) gene and non-transgenic wild-type mice at 27 weeks of age. Although the transgenic mice showed remarkable neurogenic muscular changes and a marked motor neuron loss in the anterior horn of spinal cord, the lacZ gene was widely expressed in all the injected muscles of transgenic mice as well as of wild-type mice at 7 days after the injection. In one transgenic and two wild-type mice, the lacZ gene expression was first detected in a few motor neurons of right lower cervical cord (C5-C6). These results demonstrate that an adenovirus-mediated foreign gene is transferred and expressed in skeletal muscles both of normal and transgenic mice model for familiar amyotrophic lateral sclerosis (FALS), and also, in the spinal motor neurons, may be transferred by retrograde transport from innervated muscles. (C) 1998 Elsevier Science Ireland Ltd.
引用
收藏
页码:153 / 156
页数:4
相关论文
共 16 条
  • [1] Dissociative expression of adenoviral-mediated E-coli LacZ gene between ischemic and reperfused rat brains
    Abe, K
    Setoguchi, Y
    Hayashi, T
    Itoyama, Y
    [J]. NEUROSCIENCE LETTERS, 1997, 226 (01) : 53 - 56
  • [2] In vivo adenovirus-mediated gene transfer and the expression in ischemic and reperfused rat brain
    Abe, K
    Setoguchi, Y
    Hayashi, T
    Itoyama, Y
    [J]. BRAIN RESEARCH, 1997, 763 (02) : 191 - 201
  • [3] Abe K, 1997, J NEUROSCI RES, V48, P63
  • [4] FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS (ALS) IN JAPAN ASSOCIATED WITH H46R MUTATION IN CU/ZN SUPEROXIDE-DISMUTASE GENE - A POSSIBLE NEW SUBTYPE OF FAMILIAL ALS
    AOKI, M
    OGASAWARA, M
    MATSUBARA, Y
    NARISAWA, K
    NAKAMURA, S
    ITOYAMA, Y
    ABE, K
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1994, 126 (01) : 77 - 83
  • [5] Isolation of a common receptor for coxsackie B viruses and adenoviruses 2 and 5
    Bergelson, JM
    Cunningham, JA
    Droguett, G
    KurtJones, EA
    Krithivas, A
    Hong, JS
    Horwitz, MS
    Crowell, RL
    Finberg, RW
    [J]. SCIENCE, 1997, 275 (5304) : 1320 - 1323
  • [6] DEFECTIVE AXONAL-TRANSPORT IN A TRANSGENIC MOUSE MODEL OF AMYOTROPHIC-LATERAL-SCLEROSIS
    COLLARD, JF
    COTE, F
    JULIEN, JP
    [J]. NATURE, 1995, 375 (6526) : 61 - 64
  • [7] Specific and efficient gene transfer strategy offers new potentialities for the treatment of motor neurone diseases
    Finiels, F
    Ribotta, MGY
    Barkats, M
    Samolyk, ML
    Robert, JJ
    Privat, A
    Revah, F
    Mallet, J
    [J]. NEUROREPORT, 1995, 7 (01) : 373 - 378
  • [8] GHADGE GD, 1995, GENE THER, V2, P132
  • [9] MOTOR-NEURON DEGENERATION IN MICE THAT EXPRESS A HUMAN CU,ZN SUPEROXIDE-DISMUTASE MUTATION
    GURNEY, ME
    PU, HF
    CHIU, AY
    DALCANTO, MC
    POLCHOW, CY
    ALEXANDER, DD
    CALIENDO, J
    HENTATI, A
    KWON, YW
    DENG, HX
    CHEN, WJ
    ZHAI, P
    SUFIT, RL
    SIDDIQUE, T
    [J]. SCIENCE, 1994, 264 (5166) : 1772 - 1775
  • [10] Gene therapy of murine motor neuron disease using adenoviral vectors for neurotrophic factors
    Haase, G
    Kennel, P
    Vigne, E
    Akli, S
    Revah, F
    Schmalbruch, H
    Kahn, A
    [J]. NATURE MEDICINE, 1997, 3 (04) : 429 - 436