Implementing the chick embryo model to study vestibular developmental disorders

被引:4
作者
Seal, Hayley E. [1 ]
Lilian, Sigmund J. [1 ]
Popratiloff, Anastas [1 ]
Hirsch, June C. [1 ]
Peusner, Kenna D. [1 ]
机构
[1] George Washington Univ, Dept Anat & Cell Biol, Sch Med & Hlth Sci, Washington, DC 20037 USA
关键词
inner ear pathology; otocyst rotation; vestibular nuclei neurons; TEMPORAL BONE ABNORMALITIES; INNER-EAR; CHARGE ASSOCIATION; CHILDREN; TANGENTIALIS; NEUROGENESIS; ANOMALIES; PATHWAYS;
D O I
10.1152/jn.00434.2019
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 embryonic day 2. 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 Here, we describe unpublished details on the surgical approaches to produce ARO chicks, including pitfalls and difficulties to avoid. NEW & NOTEWORTHY 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.
引用
收藏
页码:2272 / 2283
页数:12
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