Department of Otolaryngology, University of Iowa, Iowa City, IA, USA.
Hear Res. 2011 Jul;277(1-2):28-36. doi: 10.1016/j.heares.2011.03.016. Epub 2011 Apr 22.
Gene-based therapeutics are being developed as novel treatments for genetic hearing loss. One roadblock to effective gene therapy is the identification of vectors which will safely deliver therapeutics to targeted cells. The cellular heterogeneity that exists within the cochlea makes viral tropism a vital consideration for effective inner ear gene therapy. There are compelling reasons to identify a viral vector with tropism for organ of Corti supporting cells. Supporting cells are the primary expression site of connexin 26 gap junction proteins that are mutated in the most common form of congenital genetic deafness (DFNB1). Supporting cells are also primary targets for inducing hair cell regeneration. Since many genetic forms of deafness are congenital it is necessary to administer gene transfer-based therapeutics prior to the onset of significant hearing loss. We have used transuterine microinjection of the fetal murine otocyst to investigate viral tropism in the developing inner ear. For the first time we have characterized viral tropism for supporting cells following in utero delivery to their progenitors. We report the inner ear tropism and potential ototoxicity of three previously untested vectors: early-generation adenovirus (Ad5.CMV.GFP), advanced-generation adenovirus (Adf.11D) and bovine adeno-associated virus (BAAV.CMV.GFP). Adenovirus showed robust tropism for organ of Corti supporting cells throughout the cochlea but induced increased ABR thresholds indicating ototoxicity. BAAV also showed tropism for organ of Corti supporting cells, with preferential transduction toward the cochlear apex. Additionally, BAAV readily transduced spiral ganglion neurons. Importantly, the BAAV-injected ears exhibited normal hearing at 5 weeks of age when compared to non-injected ears. Our results support the use of BAAV for safe and efficient targeting of supporting cell progenitors in the developing murine inner ear.
基因治疗正被开发为治疗遗传性听力损失的新方法。有效的基因治疗的一个障碍是鉴定将治疗剂安全递送至靶细胞的载体。耳蜗内存在的细胞异质性使得病毒嗜性成为内耳基因治疗有效的重要考虑因素。有充分的理由确定一种对耳蜗支持细胞具有嗜性的病毒载体。支持细胞是连接蛋白 26 间隙连接蛋白的主要表达部位,该蛋白在最常见的先天性遗传性耳聋(DFNB1)形式中发生突变。支持细胞也是诱导毛细胞再生的主要靶标。由于许多遗传性耳聋是先天性的,因此有必要在显著听力损失发生之前进行基因转移治疗。我们使用胎儿鼠耳蜗的经子宫内微注射来研究发育中内耳的病毒嗜性。我们首次描述了在向其祖细胞体内传递后,病毒对支持细胞的嗜性。我们报告了三种以前未经过测试的载体的内耳嗜性和潜在的耳毒性:第一代腺病毒(Ad5.CMV.GFP)、第三代腺病毒(Adf.11D)和牛腺相关病毒(BAAV.CMV.GFP)。腺病毒在整个耳蜗中对耳蜗支持细胞具有很强的嗜性,但诱导 ABR 阈值升高表明其耳毒性。BAAV 也显示出对耳蜗支持细胞的嗜性,并且对耳蜗顶端具有优先转导性。此外,BAAV 容易转导螺旋神经节神经元。重要的是,与未注射的耳朵相比,注射 BAAV 的耳朵在 5 周龄时表现出正常的听力。我们的结果支持使用 BAAV 安全有效地靶向发育中小鼠内耳的支持细胞祖细胞。