PUBLICATION
Tekt3 Safeguards Proper Functions and Morphology of Neuromast Hair Bundles
- Authors
- Su, D., Lu, S., Zheng, L., Liu, D.
- ID
- ZDB-PUB-250418-4
- Date
- 2025
- Source
- International Journal of Molecular Sciences 26: (Journal)
- Registered Authors
- Keywords
- cilia, hair cell, regeneration, tekt3, zebrafish
- MeSH Terms
-
- Hair Cells, Auditory*/metabolism
- Lateral Line System/metabolism
- Mice
- Ear, Inner/metabolism
- Cilia/metabolism
- Animals
- Zebrafish Proteins*/genetics
- Zebrafish Proteins*/metabolism
- Zebrafish/genetics
- Zebrafish/metabolism
- PubMed
- 40243732 Full text @ Int. J. Mol. Sci.
Citation
Su, D., Lu, S., Zheng, L., Liu, D. (2025) Tekt3 Safeguards Proper Functions and Morphology of Neuromast Hair Bundles. International Journal of Molecular Sciences. 26:.
Abstract
The inner ear and/or lateral line are responsible for hearing and balance of vertebrate. The otic sensory hair cells (HCs) employ cilium organelles, namely stereocilia and/or kinocilia, to mediate mechanical stimuli to electrical signal transition. Tektins (Tekts) are known as the cilium microtubule stabilizer and inner-space filler, and four Tekt(1-4)-encoding genes are identified in zebrafish HCs, but the subcellular location of Tekts in HCs remains unknown. In the present study, we first found that tekt3 is expressed in the inner ear and lateral line neuromast. Antibody staining revealed that Tekt3 is present in neuromast and utricular HCs. It is absent in the saccule, the authentic hearing end-organ of zebrafish and the crista of semi-circular canals. Furthermore, Tekt3 were enriched at the apical side of neuromast and utricular HCs, mainly in the cytosol. Similar subcellular distribution of Tekt3 was also evident in the outer HCs of mature mouse cochlea, which are not directly linked to the hearing sense. However, only neuromast HCs exerted morphological defect of kinocilia in tekt3 mutant. The disrupted or distorted HC kinocilia of mutant neuromast ultimately resulted in slower vital dye intake, delayed HC regeneration after neomycin treatment, and reduced startle response to vibration stimulation. All functional defects of tekt3 mutant were largely rescued by wild-type tekt3 mRNA. Our study thus suggests that zebrafish Tekt3 maintains the integrity and function of neuromast kinocilia to against surrounding and persistent low-frequency noises, perhaps via the intracellular distribution of Tekt3. Nevertheless, TEKT3/Tekt3 could be used to clarify HC sub-types in both zebrafish and mice, to highlight the non-hearing HCs.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping