Parker Mark, Brugeaud Aurore, Edge Albert S B
Department of Otology and Laryngology, Harvard Medical School, USA.
J Vis Exp. 2010 Feb 4(36):1685. doi: 10.3791/1685.
In all mammals, the sensory epithelium for audition is located along the spiraling organ of Corti that resides within the conch shaped cochlea of the inner ear (fig 1). Hair cells in the developing cochlea, which are the mechanosensory cells of the auditory system, are aligned in one row of inner hair cells and three (in the base and mid-turns) to four (in the apical turn) rows of outer hair cells that span the length of the organ of Corti. Hair cells transduce sound-induced mechanical vibrations of the basilar membrane into neural impulses that the brain can interpret. Most cases of sensorineural hearing loss are caused by death or dysfunction of cochlear hair cells. An increasingly essential tool in auditory research is the isolation and in vitro culture of the organ explant. Once isolated, the explants may be utilized in several ways to provide information regarding normative, anomalous, or therapeutic physiology. Gene expression, stereocilia motility, cell and molecular biology, as well as biological approaches for hair cell regeneration are examples of experimental applications of organ of Corti explants. This protocol describes a method for the isolation and culture of the organ of Corti from neonatal mice. The accompanying video includes stepwise directions for the isolation of the temporal bone from mouse pups, and subsequent isolation of the cochlea, spiral ligament, and organ of Corti. Once isolated, the sensory epithelium can be plated and cultured in vitro in its entirety, or as a further dissected micro-isolate that lacks the spiral limbus and spiral ganglion neurons. Using this method, primary explants can be maintained for 7-10 days. As an example of the utility of this procedure, organ of Corti explants will be electroporated with an exogenous DsRed reporter gene. This method provides an improvement over other published methods because it provides reproducible, unambiguous, and stepwise directions for the isolation, microdissection, and primary culture of the organ of Corti.
在所有哺乳动物中,听觉的感觉上皮沿着位于内耳海螺状耳蜗内的柯蒂氏器呈螺旋状分布(图1)。发育中的耳蜗中的毛细胞是听觉系统的机械感觉细胞,它们排成一排内毛细胞以及三排(在基部和中部转弯处)到四排(在顶部转弯处)外毛细胞,跨越柯蒂氏器的长度。毛细胞将基底膜的声音诱导机械振动转化为大脑能够解读的神经冲动。大多数感音神经性听力损失病例是由耳蜗毛细胞的死亡或功能障碍引起的。听觉研究中一个越来越重要的工具是器官外植体的分离和体外培养。一旦分离出来,外植体可以通过多种方式用于提供有关正常、异常或治疗生理学的信息。基因表达、静纤毛运动、细胞和分子生物学以及毛细胞再生的生物学方法都是柯蒂氏器外植体实验应用的例子。本方案描述了一种从新生小鼠分离和培养柯蒂氏器的方法。随附的视频包括从幼鼠分离颞骨以及随后分离耳蜗、螺旋韧带和柯蒂氏器的逐步指导。一旦分离出来,感觉上皮可以整体铺板并在体外培养,或者作为进一步解剖的微分离物,不包括螺旋缘和螺旋神经节神经元。使用这种方法,原代外植体可以维持7 - 10天。作为该程序实用性的一个例子,柯蒂氏器外植体将用外源DsRed报告基因进行电穿孔。这种方法比其他已发表的方法有所改进,因为它为柯蒂氏器的分离、显微解剖和原代培养提供了可重复、明确且逐步的指导。