scholarly journals Cilia in the developing zebrafish ear

2019 ◽  
Vol 375 (1792) ◽  
pp. 20190163 ◽  
Author(s):  
Tanya T. Whitfield

The inner ear, which mediates the senses of hearing and balance, derives from a simple ectodermal vesicle in the vertebrate embryo. In the zebrafish, the otic placode and vesicle express a whole suite of genes required for ciliogenesis and ciliary motility. Every cell of the otic epithelium is ciliated at early stages; at least three different ciliary subtypes can be distinguished on the basis of length, motility, genetic requirements and function. In the early otic vesicle, most cilia are short and immotile. Long, immotile kinocilia on the first sensory hair cells tether the otoliths, biomineralized aggregates of calcium carbonate and protein. Small numbers of motile cilia at the poles of the otic vesicle contribute to the accuracy of otolith tethering, but neither the presence of cilia nor ciliary motility is absolutely required for this process. Instead, otolith tethering is dependent on the presence of hair cells and the function of the glycoprotein Otogelin. Otic cilia or ciliary proteins also mediate sensitivity to ototoxins and coordinate responses to extracellular signals. Other studies are beginning to unravel the role of ciliary proteins in cellular compartments other than the kinocilium, where they are important for the integrity and survival of the sensory hair cell. This article is part of the Theo Murphy meeting issue ‘Unity and diversity of cilia in locomotion and transport’.

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Ruishuang Geng ◽  
David N Furness ◽  
Chithra K Muraleedharan ◽  
Jinsheng Zhang ◽  
Alain Dabdoub ◽  
...  

Development ◽  
2012 ◽  
Vol 139 (10) ◽  
pp. 1777-1787 ◽  
Author(s):  
G. A. Stooke-Vaughan ◽  
P. Huang ◽  
K. L. Hammond ◽  
A. F. Schier ◽  
T. T. Whitfield

2015 ◽  
Vol 108 (2) ◽  
pp. 506a
Author(s):  
Xiao-Ping Liu ◽  
Bifeng Pan ◽  
Yukako Asai ◽  
Kyoto Kurima ◽  
Andrew J. Griffith ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-9
Author(s):  
Joel Sng ◽  
Thomas Lufkin

The inner ear cytoarchitecture forms one of the most intricate and delicate organs in the human body and is vulnerable to the effects of genetic disorders, aging, and environmental damage. Owing to the inability of the mammalian cochlea to regenerate sensory hair cells, the loss of hair cells is a leading cause of deafness in humans. Millions of individuals worldwide are affected by the emotionally and financially devastating effects of hearing impairment (HI). This paper provides a brief introduction into the key role of genes regulating inner ear development and function. Potential future therapies that leverage on an improved understanding of these molecular pathways are also described in detail.


2015 ◽  
Vol 112 (12) ◽  
pp. 3746-3751 ◽  
Author(s):  
Eun Jin Son ◽  
Ji-Hyun Ma ◽  
Harinarayana Ankamreddy ◽  
Jeong-Oh Shin ◽  
Jae Young Choi ◽  
...  

Sound frequency discrimination begins at the organ of Corti in mammals and the basilar papilla in birds. Both of these hearing organs are tonotopically organized such that sensory hair cells at the basal (proximal) end respond to high frequency sound, whereas their counterparts at the apex (distal) respond to low frequencies. Sonic hedgehog (Shh) secreted by the developing notochord and floor plate is required for cochlear formation in both species. In mice, the apical region of the developing cochlea, closer to the ventral midline source of Shh, requires higher levels of Shh signaling than the basal cochlea farther away from the midline. Here, gain-of-function experiments using Shh-soaked beads in ovo or a mouse model expressing constitutively activated Smoothened (transducer of Shh signaling) show up-regulation of apical genes in the basal cochlea, even though these regionally expressed genes are not necessarily conserved between the two species. In chicken, these altered gene expression patterns precede morphological and physiological changes in sensory hair cells that are typically associated with tonotopy such as the total number of stereocilia per hair cell and gene expression of an inward rectifier potassium channel, IRK1, which is a bona fide feature of apical hair cells in the basilar papilla. Furthermore, our results suggest that this conserved role of Shh in establishing cochlear tonotopy is initiated early in development by Shh emanating from the notochord and floor plate.


1977 ◽  
Vol 55 (1) ◽  
pp. 223-230 ◽  
Author(s):  
F. Ramprashad ◽  
K. Ronald

Surface preparations of the organ of Corti of four harp seals were used to study the effect of prolonged ingestion of methyl mercury on the sensory cell population.A low level of damage to the sensory hair cells occurred throughout the length of the cochlea. Damage was confined to the three outer rows of sensory hair cells especially the third outermost row. At each location along the length of the cochlea, sensory hair cell damage in the seals on a daily dose of 25.0 mg/kg of methyl mercury exceeded the damage to the cochlea of the seals fed on a daily dose of 0.25 mg/kg of methyl mercury. Greatest damage in all the mercury-treated seals occurred in the middle coil of the cochlea. Seals on the higher mercury diet showed a 20–24% sensory cell damage at the upper middle coil, about 19–26 mm from the base, whereas only 4–5% damage was found within same region in the cochlea of the seals on the lower mercury diet.This lack of specificity and low level of damage to the sensory hair cells seems characteristic of mercury and is a direct contrast to other known ototoxic agents.


2018 ◽  
Vol 9 (1) ◽  
Author(s):  
Qiuxiang Zhang ◽  
Suna Li ◽  
Hiu-Tung C. Wong ◽  
Xinyi J. He ◽  
Alisha Beirl ◽  
...  

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