The Notch Ligand Jagged1 Is Required for the Formation, Maintenance, and Survival of Hensen's Cells in the Mouse Cochlea

被引:15
|
作者
Chrysostomou, Elena [1 ]
Zhou, Luyi [3 ]
Darcy, Yuanzhao L. [3 ]
Graves, Kaley A. [3 ]
Doetzlhofer, Angelika [1 ,2 ]
Cox, Brandon C. [3 ,4 ]
机构
[1] Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Ctr Hearing & Balance, Dept Otolaryngol Head & Neck Surg, Baltimore, MD 21205 USA
[3] Southern Illinois Univ, Sch Med, Dept Pharmacol, Springfield, IL 62702 USA
[4] Southern Illinois Univ, Sch Med, Dept Otolaryngol, Springfield, IL 62702 USA
来源
JOURNAL OF NEUROSCIENCE | 2020年 / 40卷 / 49期
关键词
Claudius cells; cochlea development; Hensen's cells; Jagged1; Notch; supporting cells; INNER-EAR DEVELOPMENT; HAIR-CELL; SUPPORTING CELLS; LATERAL INDUCTION; REGULATES DEVELOPMENT; PROGENITOR CELLS; EXPRESSION; ORGAN; FATE; GENE;
D O I
10.1523/JNEUROSCI.1192-20.2020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
During cochlear development, the Notch ligand JAGGED 1 (JAG1) plays an important role in the specification of the prosensory region, which gives rise to sound-sensing hair cells and neighboring supporting cells (SCs). While JAG1's expression is maintained in SCs through adulthood, the function of JAG1 in SC development is unknown. Here, we demonstrate that JAG1 is essential for the formation and maintenance of Hensen's cells, a highly specialized SC subtype located at the edge of the auditory epithelium. Using Sox2(CreERT2/+)::Jag1(loxP/loxP) mice of both genders, we show that Jag1 deletion at the onset of differentiation, at embryonic day 14.5, disrupted Hensen's cell formation. Similar loss of Hensen's cells was observed when Jag1 was deleted after Hensen's cell formation at postnatal day (P) 0/P1 and fate-mapping analysis revealed that in the absence of Jag1, some Hensen's cells die, but others convert into neighboring Claudius cells. In support of a role for JAG1 in cell survival, genes involved in mitochondrial function and protein synthesis were downregulated in the sensory epithelium of P0 cochlea lacking Jag1. Finally, using Fgfr3-iCreER(T2)::Jag1(loxP/loxP) mice to delete Jag1 at P0, we observed a similar loss of Hensen's cells and found that adult Jag1 mutant mice have hearing deficits at the low-frequency range.
引用
收藏
页码:9401 / 9413
页数:13
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