Ptch1 is essential for cochlear marginal cell differentiation and stria vascularis formation

被引:2
|
作者
Qin, Tianli [1 ,2 ]
So, Karl Kam Hei [1 ]
Hui, Chi-Chung [3 ,4 ]
Sham, Mai Har [1 ]
机构
[1] Chinese Univ Hong Kong, Sch Biomed Sci, Shatin, Hong Kong, Peoples R China
[2] Univ Hong Kong, Li Ka Shing Fac Med, Sch Biomed Sci, Pokfulam, Hong Kong, Peoples R China
[3] Hosp Sick Children, Program Dev & Stem Cell Biol, Toronto, ON M5G 0A4, Canada
[4] Univ Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
来源
CELL REPORTS | 2024年 / 43卷 / 04期
基金
加拿大健康研究院;
关键词
CONNEXIN; 26; INNER-EAR; GLI2; SUPPRESSOR; MUTATIONS; RECEPTOR; DEFECTS; CHANNEL; JERVELL; SUFU;
D O I
10.1016/j.celrep.2024.114083
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A common cause of deafness in humans is dysregulation of the endocochlear potential generated by the stria vascularis (SV). Thus, proper formation of the SV is critical for hearing. Using single -cell transcriptomics and a series of Shh signaling mutants, we discovered that the Shh receptor Patched1 (Ptch1) is essential for marginal cell (MC) differentiation and SV formation. Single -cell RNA sequencing analyses revealed that the cochlear roof epithelium is already specified into discrete domains with distinctive gene expression profiles at embryonic day 14, with Gsc as a marker gene of the MC lineage. Ptch1 deficiency leads to defective specification of MC precursors along the cochlear basal -apical regions. We demonstrated that elevated Gli2 levels impede MC differentiation through sustaining Otx2 expression and maintaining the progenitor state of MC precursors. Our results uncover an early specification of cochlear non -sensory epithelial cells and establish a crucial role of the Ptch1-Gli2 axis in regulating the development of SV.
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页数:16
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