Literature DB >> 16600188

The paintfill method as a tool for analyzing the three-dimensional structure of the inner ear.

Amy E Kiernan1.   

Abstract

The mammalian inner ear is a complex epithelial tube designed to detect sound, angular and linear acceleration, as well as gravity. The major parts of the ear include three orthogonal semicircular canals, a central vestibule, a coiled cochlea, and an endolymphatic duct and sac allowing fluid balance with the cerebrospinal system. Located throughout this tubular system are six separate sensory areas composed of hair cells and support cells that are essential for the transduction of hearing and balance information. Deafness and vestibular dysfunction are extremely common sensory disorders in the human population, with one in every 1000 children born profoundly hearing impaired and many progressive forms diagnosed later in life. Approximately 20-30% of patients with congenital sensorineural hearing loss demonstrate radiographic abnormalities of the inner ear, indicating that malformations of the inner ear make a significant contribution to the high frequency of deafness and balance disorders. Unfortunately, the very complexity that makes the inner ear such an exquisite structure has also made it an extremely difficult organ to tackle for researchers. Here, I describe a histological method involving paintfilling of the inner ear that provides easy analysis of the three-dimensional structure of this complex organ. The paintfill method can be used to quickly assess inner ear morphology and can help identify defects that may cause or contribute to deafness and/or vestibular dysfunction.

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Year:  2006        PMID: 16600188     DOI: 10.1016/j.brainres.2006.02.037

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  24 in total

1.  Canonical Notch signaling is not necessary for prosensory induction in the mouse cochlea: insights from a conditional mutant of RBPjkappa.

Authors:  Martín L Basch; Takahiro Ohyama; Neil Segil; Andrew K Groves
Journal:  J Neurosci       Date:  2011-06-01       Impact factor: 6.167

2.  A spontaneous mouse deletion in Mctp1 uncovers a long-range cis-regulatory region crucial for NR2F1 function during inner ear development.

Authors:  Basile Tarchini; Chantal Longo-Guess; Cong Tian; Abigail L D Tadenev; Nicholas Devanney; Kenneth R Johnson
Journal:  Dev Biol       Date:  2018-09-11       Impact factor: 3.582

3.  TBX1 is required for normal stria vascularis and semicircular canal development.

Authors:  Cong Tian; Kenneth R Johnson
Journal:  Dev Biol       Date:  2019-09-21       Impact factor: 3.582

4.  Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice.

Authors:  Kenneth R Johnson; Leona H Gagnon; Cong Tian; Chantal M Longo-Guess; Benjamin E Low; Michael V Wiles; Amy E Kiernan
Journal:  Genetics       Date:  2018-01-03       Impact factor: 4.562

5.  SOX2 is required for inner ear growth and cochlear nonsensory formation before sensory development.

Authors:  Aleta R Steevens; Jenna C Glatzer; Courtney C Kellogg; Walter C Low; Peter A Santi; Amy E Kiernan
Journal:  Development       Date:  2019-06-21       Impact factor: 6.868

6.  Compensatory regulation of the size of the inner ear in response to excess induction of otic progenitors by fibroblast growth factor signaling.

Authors:  Jian Zhang; Kevin D Wright; Amanda A Mahoney Rogers; Molly M Barrett; Katherine Shim
Journal:  Dev Dyn       Date:  2014-06-12       Impact factor: 3.780

Review 7.  Segregating neural and mechanosensory fates in the developing ear: patterning, signaling, and transcriptional control.

Authors:  Steven Raft; Andrew K Groves
Journal:  Cell Tissue Res       Date:  2014-06-06       Impact factor: 5.249

8.  Fgf10 is required for specification of non-sensory regions of the cochlear epithelium.

Authors:  Lisa D Urness; Xiaofen Wang; Shumei Shibata; Takahiro Ohyama; Suzanne L Mansour
Journal:  Dev Biol       Date:  2015-01-24       Impact factor: 3.582

9.  Genetic background modifies inner ear and eye phenotypes of jag1 heterozygous mice.

Authors:  Amy E Kiernan; Renhua Li; Norman L Hawes; Gary A Churchill; Thomas Gridley
Journal:  Genetics       Date:  2007-09       Impact factor: 4.562

10.  Catweasel mice: a novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndrome.

Authors:  Erika A Bosman; Elizabeth Quint; Helmut Fuchs; Martin Hrabé de Angelis; Karen P Steel
Journal:  Dev Biol       Date:  2009-02-02       Impact factor: 3.582

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