Seal Hayley E, Lilian Sigmund J, Popratiloff Anastas, Hirsch June C, Peusner Kenna D
Department of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, District of Columbia.
J Neurophysiol. 2019 Dec 1;122(6):2272-2283. doi: 10.1152/jn.00434.2019. Epub 2019 Oct 2.
Children with congenital vestibular disorders show delayed motor development and challenges in maintaining posture and balance. Computed tomography images reveal that these children have abnormal inner ears in the form of a sac, with the semicircular canals missing or truncated. Little is known about how this inner ear abnormality affects central vestibular development. At present, mice with the chromodomain helicase DNA-binding protein 7 mutation are the most common model for studying congenital vestibular disorders, despite forming multiple diverse inner ear phenotypes and inducing abnormal cerebellar and visual system development. To identify the effects of a sac-like inner ear on central vestibular development, we have designed and implemented a new model, the anterior-posterior axis rotated otocyst (ARO) chick, which forms a sac-like inner ear in 85% of cases. The ARO chick is produced by anterior-posterior rotation of the otocyst at . Here, we describe for the first time the 15% of ARO chicks that form three small semicircular canals and rename the ARO chicks forming sacs (ARO/s chicks). The basic features of the vestibular sensory organs in ARO/s chicks are similar to those found in patients' sacs, and ARO/s hatchlings experience balance and walking problems like patients. Thus, ARO/s chicks have a reproducible inner ear phenotype without abnormalities in vestibular-related structures, making the model a relatively simple one to evaluate the relationship between the sac-like inner ear pathology and formation of the central vestibular neural circuitry. Here, we describe unpublished details on the surgical approaches to produce ARO chicks, including pitfalls and difficulties to avoid. This paper describes simple techniques for chick otocyst rotation resulting in a sac-like inner ear (85%), the common phenotype in congenital vestibular disorders. We now describe anterior-posterior axis rotated otocyst chicks, which form three small canals (15%), and rename chicks forming a sac (ARO/s chicks). Basic protocols and potential complications of otocyst rotation are described. With the use of ARO/s chicks, it will be possible to determine how the vestibular neural circuit is modified by sac-like inner ear formation.
患有先天性前庭疾病的儿童表现出运动发育迟缓,在维持姿势和平衡方面存在困难。计算机断层扫描图像显示,这些儿童的内耳呈囊状异常,半规管缺失或截断。关于这种内耳异常如何影响中枢前庭发育,人们知之甚少。目前,尽管携带色域解旋酶DNA结合蛋白7突变的小鼠会形成多种不同的内耳表型,并导致小脑和视觉系统发育异常,但它们是研究先天性前庭疾病最常用的模型。为了确定囊状内耳对中枢前庭发育的影响,我们设计并实施了一种新模型,即前后轴旋转耳囊(ARO)小鸡,该模型在85%的情况下会形成囊状内耳。ARO小鸡是通过在特定阶段将耳囊进行前后旋转产生的。在此,我们首次描述了15%的ARO小鸡会形成三个小半规管,并将形成囊状的ARO小鸡重新命名为ARO/s小鸡。ARO/s小鸡前庭感觉器官的基本特征与患者囊状内耳的特征相似,并且ARO/s幼雏也像患者一样存在平衡和行走问题。因此,ARO/s小鸡具有可重复的内耳表型,且前庭相关结构无异常,这使得该模型成为评估囊状内耳病变与中枢前庭神经回路形成之间关系的相对简单的模型。在此处,我们描述了关于产生ARO小鸡的手术方法的未发表细节,包括需要避免的陷阱和困难。本文描述了导致囊状内耳(85%,先天性前庭疾病中的常见表型)的小鸡耳囊旋转的简单技术。我们现在描述形成三个小半规管(15%)的前后轴旋转耳囊小鸡,并重新命名形成囊状的小鸡为ARO/s小鸡。描述了耳囊旋转的基本方案和潜在并发症。通过使用ARO/s小鸡,将有可能确定前庭神经回路如何因囊状内耳的形成而发生改变。