A novel bovine virus efficiently transduces inner ear neuroepithelial cells

被引:28
作者
Di Pasquale, G
Rzadzinska, A
Schneider, ME
Bossis, I
Chiorini, JA
Kachar, B
机构
[1] Natl Inst Dental & Craniofacial Res, Gene Therapy & Therapeut Branch, NIH, US Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[2] Natl Inst Deafness & Other Commun Disorders, Sect Struct Cell Biol, NIH, US Dept Hlth & Human Serv, Bethesda, MD 20892 USA
关键词
BAAV; AAV; adeno-associated virus; hair cells; inner ear; stereocilia;
D O I
10.1016/j.ymthe.2005.02.004
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
Disruption of the cellular composition or arrangement of the sensory epithelia due to hair cell or supporting cell damage leads to hearing loss and vestibular dysfunctions. These peripheral hearing disorders make good targets for gene therapy; however, development requires efficient gene transfer methods for the inner ear. Here we characterized the cellular tropism of a novel adeno-associated bovine virus vector (BAAV) in cultured rat inner ear epithelia. To help identify transduced cells, we used beta-actin-GFP as a reporter gene. We found that BAAV efficiently transduced auditory and vestibular hair cells as well as all types of supporting cells with no apparent pathological effects. The number of transduced hair cells significantly increased in both a dose- and a time-dependent manner. Transduction was independent of the cells' maturation state and was observed in both P2 and P10 cultures. Interestingly, even after several days of incubation with BAAV, hair cells demonstrated varying progression of beta-actin-GFP incorporation into the stereocilia. This suggests that the onset of viral transduction can occur throughout the course of the experiment. Of the other tested AAVs, AAV2 and AAV5 transduced only a small percentage of inner and vestibular hair cells, respectively, whereas no transduction was detected with AAV4.
引用
收藏
页码:849 / 855
页数:7
相关论文
共 39 条
[1]   Cloning of an avian adeno-associated virus (AAAV) and generation of recombinant AAAV particles [J].
Bossis, I ;
Chiorini, JA .
JOURNAL OF VIROLOGY, 2003, 77 (12) :6799-6810
[2]   Neurotrophin-3 transduction attenuates cisplatin spiral ganglion neuron ototoxicity in the cochlea [J].
Bowers, WJ ;
Chen, XW ;
Guo, H ;
Frisina, DR ;
Federoff, HJ ;
Frisina, RD .
MOLECULAR THERAPY, 2002, 6 (01) :12-18
[3]   HSV amplicon-mediated neurotrophin-3 expression protects murine spiral ganglion neurons from cisplatin-induced damage [J].
Chen, XW ;
Frisina, RD ;
Bowers, WJ ;
Frisina, DR ;
Federoff, HJ .
MOLECULAR THERAPY, 2001, 3 (06) :958-963
[4]   Cloning of adeno-associated virus type 4 (AAV4) and generation of recombinant AAV4 particles [J].
Chiorini, JA ;
Yang, L ;
Liu, YJ ;
Safer, B ;
Kotin, RM .
JOURNAL OF VIROLOGY, 1997, 71 (09) :6823-6833
[5]   Cloning and characterization of adeno-associated virus type 5 [J].
Chiorini, JA ;
Kim, F ;
Yang, L ;
Kotin, RM .
JOURNAL OF VIROLOGY, 1999, 73 (02) :1309-1319
[6]   Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death [J].
Cohen-Salmon, M ;
Ott, T ;
Michel, V ;
Hardelin, JP ;
Perfettini, I ;
Eybalin, M ;
Wu, T ;
Marcus, DC ;
Wangemann, P ;
Willecke, K ;
Petit, C .
CURRENT BIOLOGY, 2002, 12 (13) :1106-1111
[7]  
Davidson Beverly L, 2003, Methods Mol Med, V76, P269
[8]   Recombinant adeno-associated virus type 2, 4, and 5 vectors: Transduction of variant cell types and regions in the mammalian central nervous system [J].
Davidson, BL ;
Stein, CS ;
Heth, JA ;
Martins, I ;
Kotin, RM ;
Derksen, TA ;
Zabner, J ;
Ghodsi, A ;
Chiorini, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3428-3432
[9]   Gene transfer into the mammalian inner ear using HSV-1 and vaccinia virus vectors [J].
Derby, ML ;
Sena-Esteves, M ;
Breakefield, XO ;
Corey, DP .
HEARING RESEARCH, 1999, 134 (1-2) :1-8
[10]   Identification of PDGFR as a receptor for AAV-5 transduction [J].
Di Pasquale, G ;
Davidson, BL ;
Stein, CS ;
Martins, IS ;
Scudiero, D ;
Monks, A ;
Chiorini, JA .
NATURE MEDICINE, 2003, 9 (10) :1306-1312