Literature DB >> 25381571

Inner ear development: building a spiral ganglion and an organ of Corti out of unspecified ectoderm.

Bernd Fritzsch1, Ning Pan, Israt Jahan, Karen L Elliott.   

Abstract

The mammalian inner ear develops from a placodal thickening into a complex labyrinth of ducts with five sensory organs specialized to detect position and movement in space. The mammalian ear also develops a spiraled cochlear duct containing the auditory organ, the organ of Corti (OC), specialized to translate sound into hearing. Development of the OC from a uniform sheet of ectoderm requires unparalleled precision in the topological developmental engineering of four different general cell types, namely sensory neurons, hair cells, supporting cells, and general otic epithelium, into a mosaic of ten distinctly recognizable cell types in and around the OC, each with a unique distribution. Moreover, the OC receives unique innervation by ear-derived spiral ganglion afferents and brainstem-derived motor neurons as efferents and requires neural-crest-derived Schwann cells to form myelin and neural-crest-derived cells to induce the stria vascularis. This transformation of a sheet of cells into a complicated interdigitating set of cells necessitates the orchestrated expression of multiple transcription factors that enable the cellular transformation from ectoderm into neurosensory cells forming the spiral ganglion neurons (SGNs), while simultaneously transforming the flat epithelium into a tube, the cochlear duct, housing the OC. In addition to the cellular and conformational changes forming the cochlear duct with the OC, changes in the surrounding periotic mesenchyme form passageways for sound to stimulate the OC. We review molecular developmental data, generated predominantly in mice, in order to integrate the well-described expression changes of transcription factors and their actions, as revealed in mutants, in the formation of SGNs and OC in the correct position and orientation with suitable innervation. Understanding the molecular basis of these developmental changes leading to the formation of the mammalian OC and highlighting the gaps in our knowledge might guide in vivo attempts to regenerate this most complicated cellular mosaic of the mammalian body for the reconstitution of hearing in a rapidly growing population of aging people suffering from hearing loss.

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Year:  2014        PMID: 25381571      PMCID: PMC4426086          DOI: 10.1007/s00441-014-2031-5

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  136 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.  Dual embryonic origin of the mammalian otic vesicle forming the inner ear.

Authors:  Laina Freyer; Vimla Aggarwal; Bernice E Morrow
Journal:  Development       Date:  2011-12       Impact factor: 6.868

3.  Ancient deuterostome origins of vertebrate brain signalling centres.

Authors:  Ariel M Pani; Erin E Mullarkey; Jochanan Aronowicz; Stavroula Assimacopoulos; Elizabeth A Grove; Christopher J Lowe
Journal:  Nature       Date:  2012-03-14       Impact factor: 49.962

Review 4.  The genesis of neural crest and epidermal placodes: a reinterpretation of vertebrate origins.

Authors:  R G Northcutt; C Gans
Journal:  Q Rev Biol       Date:  1983-03       Impact factor: 4.875

5.  Pax2 contributes to inner ear patterning and optic nerve trajectory.

Authors:  M Torres; E Gómez-Pardo; P Gruss
Journal:  Development       Date:  1996-11       Impact factor: 6.868

6.  The Atoh1-lineage gives rise to hair cells and supporting cells within the mammalian cochlea.

Authors:  Elizabeth Carroll Driver; Laura Sillers; Thomas M Coate; Matthew F Rose; Matthew W Kelley
Journal:  Dev Biol       Date:  2013-01-11       Impact factor: 3.582

7.  Disruption of fibroblast growth factor receptor 3 signaling results in defects in cellular differentiation, neuronal patterning, and hearing impairment.

Authors:  Chandrakala Puligilla; Feng Feng; Kotaro Ishikawa; Stefano Bertuzzi; Alain Dabdoub; Andrew J Griffith; Bernd Fritzsch; Matthew W Kelley
Journal:  Dev Dyn       Date:  2007-07       Impact factor: 3.780

8.  Sox2 is required for sensory organ development in the mammalian inner ear.

Authors:  Amy E Kiernan; Anna L Pelling; Keith K H Leung; Anna S P Tang; Donald M Bell; Charles Tease; Robin Lovell-Badge; Karen P Steel; Kathryn S E Cheah
Journal:  Nature       Date:  2005-04-21       Impact factor: 49.962

9.  The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype.

Authors:  Sally H Cross; Lisa McKie; Katrine West; Emma L Coghill; Jack Favor; Shoumo Bhattacharya; Steve D M Brown; Ian J Jackson
Journal:  Hum Mol Genet       Date:  2010-10-13       Impact factor: 6.150

10.  Differentiation of the lateral compartment of the cochlea requires a temporally restricted FGF20 signal.

Authors:  Sung-Ho Huh; Jennifer Jones; Mark E Warchol; David M Ornitz
Journal:  PLoS Biol       Date:  2012-01-03       Impact factor: 8.029

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  34 in total

1.  Spatio-temporal dynamics of β-tubulin isotypes during the development of the sensory auditory organ in rat.

Authors:  Justine Renauld; Nicolas Johnen; Nicolas Thelen; Marie Cloes; Marc Thiry
Journal:  Histochem Cell Biol       Date:  2015-07-26       Impact factor: 4.304

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.  Deterioration of the Medial Olivocochlear Efferent System Accelerates Age-Related Hearing Loss in Pax2-Isl1 Transgenic Mice.

Authors:  Tetyana Chumak; Romana Bohuslavova; Iva Macova; Nicole Dodd; Daniela Buckiova; Bernd Fritzsch; Josef Syka; Gabriela Pavlinkova
Journal:  Mol Neurobiol       Date:  2015-05-20       Impact factor: 5.590

4.  Ear manipulations reveal a critical period for survival and dendritic development at the single-cell level in Mauthner neurons.

Authors:  Karen L Elliott; Douglas W Houston; Rhonda DeCook; Bernd Fritzsch
Journal:  Dev Neurobiol       Date:  2015-03-20       Impact factor: 3.964

5.  Npr2 null mutants show initial overshooting followed by reduction of spiral ganglion axon projections combined with near-normal cochleotopic projection.

Authors:  Hannes Schmidt; Bernd Fritzsch
Journal:  Cell Tissue Res       Date:  2019-06-14       Impact factor: 5.249

6.  Understanding Molecular Evolution and Development of the Organ of Corti Can Provide Clues for Hearing Restoration.

Authors:  Israt Jahan; Karen L Elliott; Bernd Fritzsch
Journal:  Integr Comp Biol       Date:  2018-08-01       Impact factor: 3.326

7.  Auditory system: development, genetics, function, aging, and diseases.

Authors:  Bernd Fritzsch; Marlies Knipper; Eckhard Friauf
Journal:  Cell Tissue Res       Date:  2015-07       Impact factor: 5.249

8.  Fbxo2VHC mouse and embryonic stem cell reporter lines delineate in vitro-generated inner ear sensory epithelia cells and enable otic lineage selection and Cre-recombination.

Authors:  Byron H Hartman; Robert Bӧscke; Daniel C Ellwanger; Sawa Keymeulen; Mirko Scheibinger; Stefan Heller
Journal:  Dev Biol       Date:  2018-09-01       Impact factor: 3.582

Review 9.  Gene, cell, and organ multiplication drives inner ear evolution.

Authors:  Bernd Fritzsch; Karen L Elliott
Journal:  Dev Biol       Date:  2017-09-01       Impact factor: 3.582

Review 10.  Neural crest contributions to the ear: Implications for congenital hearing disorders.

Authors:  K Elaine Ritter; Donna M Martin
Journal:  Hear Res       Date:  2018-11-14       Impact factor: 3.208

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