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TUBB4B is essential for the cytoskeletal architecture of cochlear supporting cells and motile cilia development
Microtubules are essential for various cellular processes. The functional diversity of microtubules is attributed to the incorporation of various α- and β-tubulin isotypes encoded by different genes. In this work, we investigated the functional role of β4B-tubulin isotype (TUBB4B) in hearing and vis...
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Published in: | Communications biology 2024-09, Vol.7 (1), p.1146-18, Article 1146 |
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Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Microtubules are essential for various cellular processes. The functional diversity of microtubules is attributed to the incorporation of various α- and β-tubulin isotypes encoded by different genes. In this work, we investigated the functional role of β4B-tubulin isotype (TUBB4B) in hearing and vision as mutations in
TUBB4B
are associated with sensorineural disease. Using a
Tubb4b
knockout mouse model, our findings demonstrate that TUBB4B is essential for hearing. Mice lacking TUBB4B are profoundly deaf due to defects in the inner and middle ear. Specifically, in the inner ear, the absence of TUBB4B lead to disorganized and reduced densities of microtubules in pillar cells, suggesting a critical role for TUBB4B in providing mechanical support for auditory transmission. In the middle ear,
Tubb4b
−/−
mice exhibit motile cilia defects in epithelial cells, leading to the development of otitis media. However,
Tubb4b
deletion does not affect photoreceptor function or cause retinal degeneration. Intriguingly, β6-tubulin levels increase in retinas lacking β4B-tubulin isotype, suggesting a functional compensation mechanism. Our findings illustrate the essential roles of TUBB4B in hearing but not in vision in mice, highlighting the distinct functions of tubulin isotypes in different sensory systems.
Mice lacking TUBB4B are profoundly deaf due to defects in both the middle and inner ear consisting in microtubule alterations in cochlear supporting cells and motile cilia defects in epithelial cells. |
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ISSN: | 2399-3642 2399-3642 |
DOI: | 10.1038/s42003-024-06867-2 |