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  3. Clinical Laboratory Sciences and Medical Biotechnology / 醫學檢驗暨生物技術學系所
  4. Critical role of hepsin/TMPRSS1 in hearing and tectorial membrane morphogenesis: Insights from transgenic mouse models.
 
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Critical role of hepsin/TMPRSS1 in hearing and tectorial membrane morphogenesis: Insights from transgenic mouse models.

Journal
Hearing research
Journal Volume
453
ISSN
1878-5891
Date Issued
2024-11
Author(s)
TING-HUA YANG  
Hsu, Yu-Chen
Yeh, Peng
Hung, Chia-Jui
Tsai, Yu-Fei
Fang, Mo-Chu
Yen, Alice Chih Chia
Chen, Li-Fu
Pan, Jhih-Yu
Chung, Fong-Ling
CHEN-CHI WU  
Yu, Wei-Ming
SHU-WHA LIN  
TIEN-CHEN LIU  
DOI
10.1016/j.heares.2024.109134
DOI
10.1016/j.heares.2024.109134
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/723865
Abstract
Mutations in various type II transmembrane serine protease (TMPRSS) family members are associated with non-syndromic hearing loss, with some mechanisms still unclear. For instance, the mechanism underlying profound hearing loss and tectorial membrane (TM) malformations in hepsin/TMPRSS1 knockout (KO) mice remains elusive. In this study, we confirmed significantly elevated hearing thresholds and abnormal TM morphology in hepsin KO mice, characterized by enlarged TM with gaps and detachment from the spiral limbus. Transgenic mouse lines were created to express either wild-type or a serine protease-dead mutant of human hepsin in the KO background. The Tg68;KO line, expressing moderate levels of wild-type human hepsin in the cochlea, showed partial restoration of hearing function. Conversely, the Tg5;KO or TgRS;KO lines, with undetectable hepsin or protease-dead hepsin, did not show such improvement. Histological analyses revealed that Tg68;KO mice, but not Tg5;KO or TgRS;KO mice, had a more compact TM structure, partially attached to the spiral limbus. These results indicate that hepsin expression levels correlate with improvements in hearing and TM morphology, and its protease activity is critical for these effects. Hepsin's role was further examined by studying its relationship with α-tectorin (TECTA) and β-tectorin (TECTB), non-collagenous proteins crucial for TM formation. Hepsin was co-expressed with TECTA and TECTB in the developing cochlear epithelium. Immunostaining showed decreased levels of TECTA and TECTB in hepsin KO TM, partially restored in Tg68;KO mice. These findings suggest that hepsin is essential for proper TM morphogenesis and auditory function, potentially by proteolytic processing/maturation of TECTA and TECTB and their incorporation into the TM.
Subjects
Hearing function
Hepsin
Tectorial membrane
Tectorin
Transgenic mice
Type II transmembrane serine protease
SDGs

[SDGs]SDG2

[SDGs]SDG3

Description
Article number 109134
Type
journal article

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