赫斯1
JAG1
Notch信号通路
条件基因敲除
内耳
毛细胞
细胞生物学
生物
科尔蒂器官
耳蜗
侧抑制
前庭系统
阿拉吉尔综合征
解剖
神经科学
信号转导
表型
内分泌学
遗传学
基因
胆汁淤积
作者
Hao Jin,Robert Koesters,Maxime Bouchard,Thomas Gridley,Susanna C. Pfannenstiel,Peter K. Plinkert,Luo Zhang,Mark Praetorius
标识
DOI:10.3109/00016489.2012.690533
摘要
Conclusion: Jagged1-mediated Notch signaling regulates hair cell (HC) production in a distinct way rather than lateral inhibition mediated by Hes1 and Hes5. Jagged1 may interact with Notch3, probably via candidate downstream mediators Hesr1 and Hesr2, regulating the prosensory formation in the early stage. Objectives: To explore the function of the Jagged1-mediated Notch signaling pathway in mammalian inner ear development and its possible mechanism. Methods: Using conditional gene targeting, a novel Jagged1 conditional knockout (Jag1-cko), Pax8cre/+; Jag1flox/flox, was established. The auditory brainstem response and swim ability test were utilized to identify functional disability. The expression of Jagged1, Notch3, Hes1, Hesr1, and Hesr2 was detected by immunofluorescence and immunohistochemistry. Results: Our Jag1-cko model was established and survived well. It presented hearing impairment and balance disturbance with 'waltzing' behavior. Cochleae and vestibular apparatus were all found in our Jag1-cko model. Patch deficiency of outer hair cells (OHCs) was found on the apical and middle turns of the auditory epithelium. OHCs were totally missing on the basal turn. The stereociliary bundles were disorientated on the cristae. Unlike Hes1, no expression of Notch3, Hesr1, and Hesr2 was found on embryonic day 13.5 of the Jag1-cko model.
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