Gene transfer using bovine adeno-associated virus in the guinea pig cochlea

被引:45
作者
Shibata, S. B. [1 ,2 ]
Di Pasquale, G. [3 ]
Cortez, S. R. [1 ]
Chiorini, J. A. [3 ]
Raphael, Y. [1 ]
机构
[1] Univ Michigan, Kresge Hearing Res Inst, Dept Otolaryngol, Ann Arbor, MI 48109 USA
[2] Kansai Med Univ, Dept Otolaryngol, Osaka, Japan
[3] Natl Inst Dent & Craniofacial Res, Gene Therapy & Therapeut Branch, NIH, Bethesda, MD USA
关键词
scala media; scala tympani; bovine adeno-associated virus; INNER-EAR; TRANSGENE EXPRESSION; ADENOVIRUS-RECEPTOR; HAIR-CELLS; TRANSDUCTION; ORGAN; DELIVERY; VECTORS; CORTI;
D O I
10.1038/gt.2009.57
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gene transfer into the cells of the cochlea is useful for both research and therapy. Bovine adeno-associated virus (BAAV) is a new viral vector with potential for long-term gene expression with little or no side effects. In this study, we assessed transgene expression using BAAV with beta-actin-GFP as a reporter gene, in the cochleae of normal and deafened guinea pigs. We used two different routes to inoculate the cochlea: scala media (SM) or scala tympani (ST). Auditory brainstem response assessments were carried out before inoculation, 7 days after inoculation and immediately before killing, to assess the functional consequences of the treatment. We observed threshold shifts because of the surgical invasion, but no apparent pathology associated with the virus. Fourteen days after the injection, animals were killed and cochleae assessed histologically. Epi-fluorescence showed that BAAV transduced the supporting cells of both normal and deafened animals through SM and ST inoculations. Transgene expression in cells of the membranous labyrinth after ST inoculation is an important outcome because of the greater feasibility of this route for future clinical application. BAAV facilitates efficient transduction of the membranous labyrinth epithelium with minimum pathogenicity and may become clinically applicable for inner ear gene therapy. Gene Therapy (2009) 16, 990-997; doi: 10.1038/gt.2009.57; published online 21 May 2009
引用
收藏
页码:990 / 997
页数:8
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