Tmc Reliance Is Biased by the Hair Cell Subtype and Position Within the Ear

Hair cells are heterogenous, enabling varied roles in sensory systems. An emerging hypothesis is that the transmembrane channel-like (Tmc) proteins of the hair cell’s mechanotransduction apparatus vary within and between organs to permit encoding of different mechanical stimuli. Five anatomical vari...

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Main Authors: Shaoyuan Zhu, Zongwei Chen, Haoming Wang, Brian M. McDermott
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-01-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Tmc
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2020.570486/full
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spelling doaj-93643b34144d45879d63b43d68c9270f2021-01-07T04:18:05ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2021-01-01810.3389/fcell.2020.570486570486Tmc Reliance Is Biased by the Hair Cell Subtype and Position Within the EarShaoyuan Zhu0Shaoyuan Zhu1Zongwei Chen2Zongwei Chen3Haoming Wang4Haoming Wang5Brian M. McDermott6Brian M. McDermott7Brian M. McDermott8Brian M. McDermott9Department of Otolaryngology–Head and Neck Surgery, School of Medicine, Case Western Reserve University, Cleveland, OH, United StatesDepartment of Biology, Case Western Reserve University, Cleveland, OH, United StatesDepartment of Otolaryngology–Head and Neck Surgery, School of Medicine, Case Western Reserve University, Cleveland, OH, United StatesDepartment of Biology, Case Western Reserve University, Cleveland, OH, United StatesDepartment of Otolaryngology–Head and Neck Surgery, School of Medicine, Case Western Reserve University, Cleveland, OH, United StatesDepartment of Biology, Case Western Reserve University, Cleveland, OH, United StatesDepartment of Otolaryngology–Head and Neck Surgery, School of Medicine, Case Western Reserve University, Cleveland, OH, United StatesDepartment of Biology, Case Western Reserve University, Cleveland, OH, United StatesDepartment of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH, United StatesDepartment of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, OH, United StatesHair cells are heterogenous, enabling varied roles in sensory systems. An emerging hypothesis is that the transmembrane channel-like (Tmc) proteins of the hair cell’s mechanotransduction apparatus vary within and between organs to permit encoding of different mechanical stimuli. Five anatomical variables that may coincide with different Tmc use by a hair cell within the ear are the containing organ, cell morphology, cell position within an organ, axis of best sensitivity for the cell, and the hair bundle’s orientation within this axis. Here, we test this hypothesis in the organs of the zebrafish ear using a suite of genetic mutations. Transgenesis and quantitative measurements demonstrate two morphologically distinct hair cell types in the central thickness of a vestibular organ, the lateral crista: short and tall. In contrast to what has been observed, we find that tall hair cells that lack Tmc1 generally have substantial reductions in mechanosensitivity. In short hair cells that lack Tmc2 isoforms, mechanotransduction is largely abated. However, hair cell Tmc dependencies are not absolute, and an exceptional class of short hair cell that depends on Tmc1 is present, termed a short hair cell erratic. To further test anatomical variables that may influence Tmc use, we map Tmc1 function in the saccule of mutant larvae that depend just on this Tmc protein to hear. We demonstrate that hair cells that use Tmc1 are found in the posterior region of the saccule, within a single axis of best sensitivity, and hair bundles with opposite orientations retain function. Overall, we determine that Tmc reliance in the ear is dependent on the organ, subtype of hair cell, position within the ear, and axis of best sensitivity.https://www.frontiersin.org/articles/10.3389/fcell.2020.570486/fullhair cellhearingbalancemechanotransductionTmczebrafish
collection DOAJ
language English
format Article
sources DOAJ
author Shaoyuan Zhu
Shaoyuan Zhu
Zongwei Chen
Zongwei Chen
Haoming Wang
Haoming Wang
Brian M. McDermott
Brian M. McDermott
Brian M. McDermott
Brian M. McDermott
spellingShingle Shaoyuan Zhu
Shaoyuan Zhu
Zongwei Chen
Zongwei Chen
Haoming Wang
Haoming Wang
Brian M. McDermott
Brian M. McDermott
Brian M. McDermott
Brian M. McDermott
Tmc Reliance Is Biased by the Hair Cell Subtype and Position Within the Ear
Frontiers in Cell and Developmental Biology
hair cell
hearing
balance
mechanotransduction
Tmc
zebrafish
author_facet Shaoyuan Zhu
Shaoyuan Zhu
Zongwei Chen
Zongwei Chen
Haoming Wang
Haoming Wang
Brian M. McDermott
Brian M. McDermott
Brian M. McDermott
Brian M. McDermott
author_sort Shaoyuan Zhu
title Tmc Reliance Is Biased by the Hair Cell Subtype and Position Within the Ear
title_short Tmc Reliance Is Biased by the Hair Cell Subtype and Position Within the Ear
title_full Tmc Reliance Is Biased by the Hair Cell Subtype and Position Within the Ear
title_fullStr Tmc Reliance Is Biased by the Hair Cell Subtype and Position Within the Ear
title_full_unstemmed Tmc Reliance Is Biased by the Hair Cell Subtype and Position Within the Ear
title_sort tmc reliance is biased by the hair cell subtype and position within the ear
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2021-01-01
description Hair cells are heterogenous, enabling varied roles in sensory systems. An emerging hypothesis is that the transmembrane channel-like (Tmc) proteins of the hair cell’s mechanotransduction apparatus vary within and between organs to permit encoding of different mechanical stimuli. Five anatomical variables that may coincide with different Tmc use by a hair cell within the ear are the containing organ, cell morphology, cell position within an organ, axis of best sensitivity for the cell, and the hair bundle’s orientation within this axis. Here, we test this hypothesis in the organs of the zebrafish ear using a suite of genetic mutations. Transgenesis and quantitative measurements demonstrate two morphologically distinct hair cell types in the central thickness of a vestibular organ, the lateral crista: short and tall. In contrast to what has been observed, we find that tall hair cells that lack Tmc1 generally have substantial reductions in mechanosensitivity. In short hair cells that lack Tmc2 isoforms, mechanotransduction is largely abated. However, hair cell Tmc dependencies are not absolute, and an exceptional class of short hair cell that depends on Tmc1 is present, termed a short hair cell erratic. To further test anatomical variables that may influence Tmc use, we map Tmc1 function in the saccule of mutant larvae that depend just on this Tmc protein to hear. We demonstrate that hair cells that use Tmc1 are found in the posterior region of the saccule, within a single axis of best sensitivity, and hair bundles with opposite orientations retain function. Overall, we determine that Tmc reliance in the ear is dependent on the organ, subtype of hair cell, position within the ear, and axis of best sensitivity.
topic hair cell
hearing
balance
mechanotransduction
Tmc
zebrafish
url https://www.frontiersin.org/articles/10.3389/fcell.2020.570486/full
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