Brandon Carlene S, Voelkel-Johnson Christina, May Lindsey A, Cunningham Lisa L
Department of Pathology and Laboratory Medicine, Medical University of South Carolina, USA.
J Vis Exp. 2012 Mar 28(61):3734. doi: 10.3791/3734.
Hearing loss and balance disturbances are often caused by death of mechanosensory hair cells, which are the receptor cells of the inner ear. Since there is no cell line that satisfactorily represents mammalian hair cells, research on hair cells relies on primary organ cultures. The best-characterized in vitro model system of mature mammalian hair cells utilizes organ cultures of utricles from adult mice (Figure 1). The utricle is a vestibular organ, and the hair cells of the utricle are similar in both structure and function to the hair cells in the auditory organ, the organ of Corti. The adult mouse utricle preparation represents a mature sensory epithelium for studies of the molecular signals that regulate the survival, homeostasis, and death of these cells. Mammalian cochlear hair cells are terminally differentiated and are not regenerated when they are lost. In non-mammalian vertebrates, auditory or vestibular hair cell death is followed by robust regeneration which restores hearing and balance functions. Hair cell regeneration is mediated by glia-like supporting cells, which contact the basolateral surfaces of hair cells in the sensory epithelium. Supporting cells are also important mediators of hair cell survival and death. We have recently developed a technique for infection of supporting cells in cultured utricles using adenovirus. Using adenovirus type 5 (dE1/E3) to deliver a transgene containing GFP under the control of the CMV promoter, we find that adenovirus specifically and efficiently infects supporting cells. Supporting cell infection efficiency is approximately 25-50%, and hair cells are not infected (Figure 2). Importantly, we find that adenoviral infection of supporting cells does not result in toxicity to hair cells or supporting cells, as cell counts in Ad-GFP infected utricles are equivalent to those in non-infected utricles (Figure 3). Thus adenovirus-mediated gene expression in supporting cells of cultured utricles provides a powerful tool to study the roles of supporting cells as mediators of hair cell survival, death, and regeneration.
听力损失和平衡障碍通常是由机械感觉毛细胞死亡引起的,机械感觉毛细胞是内耳的受体细胞。由于没有能令人满意地代表哺乳动物毛细胞的细胞系,因此对毛细胞的研究依赖于原代器官培养。成熟哺乳动物毛细胞最具特征的体外模型系统利用成年小鼠椭圆囊的器官培养物(图1)。椭圆囊是一个前庭器官,椭圆囊的毛细胞在结构和功能上与听觉器官柯蒂氏器中的毛细胞相似。成年小鼠椭圆囊制剂代表了一种成熟的感觉上皮,可用于研究调节这些细胞存活、稳态和死亡的分子信号。哺乳动物耳蜗毛细胞是终末分化的,一旦丢失就不会再生。在非哺乳动物脊椎动物中,听觉或前庭毛细胞死亡后会有强大的再生过程,恢复听力和平衡功能。毛细胞再生由胶质样支持细胞介导,这些细胞与感觉上皮中毛细胞的基底外侧表面接触。支持细胞也是毛细胞存活和死亡的重要调节因子。我们最近开发了一种利用腺病毒感染培养椭圆囊中支持细胞的技术。使用5型腺病毒(dE1/E3)在巨细胞病毒启动子的控制下传递包含绿色荧光蛋白的转基因,我们发现腺病毒能特异性且高效地感染支持细胞。支持细胞的感染效率约为25%-50%,毛细胞未被感染(图2)。重要的是,我们发现腺病毒感染支持细胞不会对毛细胞或支持细胞产生毒性,因为腺病毒绿色荧光蛋白感染的椭圆囊中细胞数量与未感染的椭圆囊相当(图3)。因此,腺病毒介导的基因在培养椭圆囊支持细胞中的表达为研究支持细胞作为毛细胞存活、死亡和再生调节因子的作用提供了一个强大的工具。