A feasibility study of recombinant adeno-associated virus as a vector for transferring a target gene to retina

被引:0
作者
Wang, Jian-Ming [1 ]
Fan, Ya-Zhi [1 ]
Hui, Na [1 ]
Xiong, Lei [1 ]
Feng, Hai-Xiao [1 ]
Sun, Nai-Xue [1 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 2, Coll Med, Dept Ophthalmol, Xian 710004, Shaanxi, Peoples R China
关键词
recombinant adeno-associated virus; green fluorescent protein gene; gene transfer; retina; TRANSGENE EXPRESSION; DELIVERY;
D O I
暂无
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
AIM: To study the feasibility of recombinant adeno-associated virus (rAAV) as a vector to transfer the green fluorescent protein (GP) gene as a target gene into rabbit retina. METHODS: Intravitreal injection of rAAV-gfp was performed in either eye for each rabbit with the other eye taken as control. At the 3rd, 7th, and 14th day after injection, the eyeballs were removed, and the retinas were flat-mounted on glass slides to inspect the retinal fluorescence, respectively. RESULTS: After intravitreal injection of rAAV-gfp, the presence of fluorescent spots in the cytoplasm of retinal cells indicated that GFP gene was efficiently transferred and expressed in the rabbit retina. CONCLUSION: Recombinant adeno-assodated virus is a reliable and simple vector for transferring target gene, e.g., GFP gene, to the retina.
引用
收藏
页码:143 / 145
页数:3
相关论文
共 50 条
  • [21] Suppression of experimental uveitis by a recombinant adeno-associated virus vector encoding interleukin-1 receptor antagonist
    Tsai, Ming-Ling
    Horng, Chi-Ting
    Chen, Show-Li
    Xiao, Xiao
    Wang, Chih-Hung
    Tsao, Yeou-Ping
    MOLECULAR VISION, 2009, 15 (164-65): : 1542 - 1552
  • [22] Transfer of activation-dependent gene expression into T cell lines by recombinant adeno-associated virus
    Zhang, PX
    Fuleihan, RL
    GENE THERAPY, 1999, 6 (02) : 182 - 189
  • [23] Hepatotoxicity in Adeno-Associated Viral Vector Gene Therapy
    Jagadisan B.
    Dhawan A.
    Current Hepatology Reports, 2023, 22 (4) : 276 - 290
  • [24] A Comparison of Inducible Gene Expression Platforms: Implications for Recombinant Adeno-Associated Virus (rAAV) Vector-Mediated Ocular Gene Therapy
    Lipinski, Daniel M.
    RETINAL DEGENERATIVE DISEASES: MECHANISMS AND EXPERIMENTAL THERAPY, 2019, 1185 : 79 - 83
  • [25] Efficient photoreceptor-targeted gene expression in vivo by recombinant adeno-associated virus
    Flannery, JG
    Zolotukhin, S
    Vaquero, MI
    LaVail, MM
    Muzyczka, N
    Hauswirth, WW
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (13) : 6916 - 6921
  • [26] Chromatographic strategies for the analytical characterization of adeno-associated virus vector-based gene therapy products
    Fekete, Szabolcs
    Aebischer, Megane K.
    Imiolek, Mateusz
    Graf, Tobias
    Ruppert, Raphael
    Lauber, Matthew
    D'Atri, Valentina
    Guillarme, Davy
    TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2023, 164
  • [27] Recombinant Adeno-Associated Virus Serotype 9 Gene Therapy in Spinal Muscular Atrophy
    Kotulska, Katarzyna
    Fattal-Valevski, Aviva
    Haberlova, Jana
    FRONTIERS IN NEUROLOGY, 2021, 12
  • [28] Adeno-associated virus vector hydrogel formulations for brain cancer gene therapy applications
    Slyk, Zaneta
    Wrzesien, Robert
    Barszcz, Slawomir
    Gawrychowski, Krzysztof
    Malecki, Maciej
    BIOMEDICINE & PHARMACOTHERAPY, 2024, 170
  • [29] Hepatic Gene Transfer in Neonatal Mice by Adeno-Associated Virus Serotype 8 Vector
    Wang, Lili
    Wang, Huan
    Bell, Peter
    McMenamin, Deirdre
    Wilson, James M.
    HUMAN GENE THERAPY, 2012, 23 (05) : 533 - 539
  • [30] Little Vector, Big Gene Transduction: Fragmented Genome Reassembly of Adeno-associated Virus
    Hirsch, Matthew L.
    Agbandje-McKenna, Mavis
    Samulski, R. Jude
    MOLECULAR THERAPY, 2010, 18 (01) : 6 - 8