Adenovirus vector-mediated gene transfer into rat retinal neurons and Muller cells in vitro and in vivo

被引:10
|
作者
Fukuhara, M
Suzuki, A
Fukuda, Y
Kosaka, J
机构
[1] Osaka Univ, Sch Med, Dept Physiol, Osaka 565, Japan
[2] Osaka Med Coll, Dept Ophthalmol, Osaka 56911, Japan
关键词
adenovirus vector; CAG promoter; gene transfer; Muller cells; retina; rat;
D O I
10.1016/S0304-3940(98)00055-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The ability and efficiency of human type V adenovirus-originated vector with CAG promoter to transfer foreign genes was examined in the rat retina. We introduced the adenovirus vector, AxCALacZ with the reporter gene LacZ (beta-galactosidase gene) into cultured retinal cells, and then injected the vector suspension into the vitreous cavity of the eye. Beta-galactosidase staining was observed in both glial and neuronal cells in vitro and in Muller cells near the injection site in vivo. Adenovirus vectors with CAG promoter are useful and efficient for the expression of foreign genes in retinal cells. (C) 1998 Elsevier Science Ireland Ltd.
引用
收藏
页码:93 / 96
页数:4
相关论文
共 50 条
  • [41] Characterization of in vitro and in vivo gene transfer proplefties of adenovirus serotype 35 vector
    Sakurai, F
    Mizuguchi, H
    Yamaguchi, T
    Hayakawa, T
    MOLECULAR THERAPY, 2003, 8 (05) : 813 - 821
  • [42] Adenoviral vector-mediated transfer of the Indian hedgehog gene modulates lymphomyelopoiesis in vivo.
    Kobune, Masayoshi
    Kawano, Yutaka
    Sasaki, Katsunori
    Takimoto, Rishu
    Kato, Junji
    Hamada, Hirofomi
    Niitsu, Yoshiro
    BLOOD, 2007, 110 (11) : 655A - 655A
  • [43] USING VIRAL VECTOR-MEDIATED GENE TRANSFER TO TARGET SPECIFIC NEUROCHEMICAL PATHWAYS IN VIVO
    Benn, A.
    Teschemacher, A. G.
    Robinson, E. S. J.
    JOURNAL OF PSYCHOPHARMACOLOGY, 2011, 25 (08) : A24 - A24
  • [44] IN-VIVO ENDOTHELIAL-SPECIFIC ADENOVIRAL VECTOR-MEDIATED GENE-TRANSFER
    SCHULICK, AH
    DONG, G
    NEWMAN, KD
    VIRMANI, R
    DICHEK, DA
    CIRCULATION, 1994, 90 (04) : 517 - 517
  • [45] In vitro adenoviral vector-mediated gene delivery to nonparenchymal cells of the liver.
    Davern, TJ
    Sevcik, AM
    Bissell, MD
    HEPATOLOGY, 1999, 30 (04) : 490A - 490A
  • [46] RETROVIRUS VECTOR-MEDIATED GENE-TRANSFER INTO HEPATOCYTES
    FRIEDMANN, T
    XU, L
    WOLFF, J
    YEE, JK
    MIYANOHARA, A
    MOLECULAR BIOLOGY & MEDICINE, 1989, 6 (02) : 117 - 125
  • [47] Regulation of synovial cell function by adenovirus vector-mediated gene transduction
    Tanaka, S
    Seto, H
    Oda, H
    Nakamura, K
    ARTHRITIS RESEARCH & THERAPY, 2003, 5 (Suppl 3) : S6 - S6
  • [48] Retroviral vector-mediated gene transfer into keratocytes: in vitro effects of polybrene and protamine sulfate
    Berthold Seitz
    Edwin Baktanian
    Erlinda M. Gordon
    W. French Anderson
    Laurie LaBree
    Peter J. McDonnell
    Graefe's Archive for Clinical and Experimental Ophthalmology, 1998, 236 : 602 - 612
  • [49] AAV vector-mediated gene transfer to the brain of the cat
    Vite, CH
    Passini, MA
    McGowan, JC
    Poptani, H
    Polesky, AC
    Chambers, B
    O'Donnell, P
    Salvetti, A
    Haskins, ME
    Wolfe, JH
    MOLECULAR THERAPY, 2003, 7 (05) : S93 - S93
  • [50] Adenovirus vector-mediated Alk gene transduction to synovial cells induces chondrogenic differentiation.
    Seto, H
    Hiraoka, H
    Fujii, M
    Imamura, T
    Miyazono, K
    Kurosawa, H
    Oda, H
    Nakamura, K
    Tanaka, S
    JOURNAL OF BONE AND MINERAL RESEARCH, 2002, 17 : S401 - S401