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Jagged1-Notch2 信号在调控鼠和人中耳骨骼形态发生中的作用。

Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear.

机构信息

Eli and Edythe Broad CIRM Center for Stem Cell Biology and Regenerative Medicine, University of Southern California, Los Angeles, CA, 90033, USA.

Department of Biochemistry and Molecular Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, 90033, USA.

出版信息

Sci Rep. 2017 May 31;7(1):2497. doi: 10.1038/s41598-017-02574-7.

Abstract

Whereas Jagged1-Notch2 signaling is known to pattern the sensorineural components of the inner ear, its role in middle ear development has been less clear. We previously reported a role for Jagged-Notch signaling in shaping skeletal elements derived from the first two pharyngeal arches of zebrafish. Here we show a conserved requirement for Jagged1-Notch2 signaling in patterning the stapes and incus middle ear bones derived from the equivalent pharyngeal arches of mammals. Mice lacking Jagged1 or Notch2 in neural crest-derived cells (NCCs) of the pharyngeal arches display a malformed stapes. Heterozygous Jagged1 knockout mice, a model for Alagille Syndrome (AGS), also display stapes and incus defects. We find that Jagged1-Notch2 signaling functions early to pattern the stapes cartilage template, with stapes malformations correlating with hearing loss across all frequencies. We observe similar stapes defects and hearing loss in one patient with heterozygous JAGGED1 loss, and a diversity of conductive and sensorineural hearing loss in nearly half of AGS patients, many of which carry JAGGED1 mutations. Our findings reveal deep conservation of Jagged1-Notch2 signaling in patterning the pharyngeal arches from fish to mouse to man, despite the very different functions of their skeletal derivatives in jaw support and sound transduction.

摘要

尽管 Jagged1-Notch2 信号通路被认为是内耳感觉神经成分的模式形成信号,但它在中耳发育中的作用尚不清楚。我们之前报道了 Jagged-Notch 信号通路在塑造来自斑马鱼前两个咽弓的骨骼元素中的作用。在这里,我们展示了 Jagged1-Notch2 信号通路在哺乳动物同源咽弓中对镫骨和砧骨中耳骨骼的模式形成中具有保守的作用。Jagged1 或 Notch2 在神经嵴衍生细胞(NCC)中缺失的小鼠表现出镫骨畸形。杂合 Jagged1 敲除小鼠,一种 Alagille 综合征(AGS)的模型,也表现出镫骨和砧骨缺陷。我们发现 Jagged1-Notch2 信号通路在早期对镫骨软骨模板进行模式形成,镫骨畸形与所有频率的听力损失相关。我们在一个杂合性 JAGGED1 缺失的患者中观察到类似的镫骨缺陷和听力损失,以及近一半 AGS 患者的传导性和感觉神经性听力损失,其中许多患者携带 JAGGED1 突变。我们的研究结果表明,Jagged1-Notch2 信号通路在从鱼类到小鼠到人中对咽弓的模式形成具有深度保守性,尽管它们的骨骼衍生物在颌骨支撑和声音转导中的功能非常不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e38/5451394/57be67966794/41598_2017_2574_Fig1_HTML.jpg

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