Literature DB >> 18571907

Cochlear stem/progenitor cells from a postnatal cochlea respond to Jagged1 and demonstrate that notch signaling promotes sphere formation and sensory potential.

Etienne Savary1, Jean Charles Sabourin, Julien Santo, Jean Philippe Hugnot, Christian Chabbert, Thomas Van De Water, Alain Uziel, Azel Zine.   

Abstract

Hair cells and supporting cells of the mammalian cochlea terminally differentiate during development. Recent in vitro evidence suggests the presence of hair cell progenitors in the postnatal cochlea. Phenotypic properties of these cells and factors that promote their ability to generate spheres in aggregate cultures have not been reported. We define an in vitro system that allows stem/progenitor cells harvested from the early postnatal cochlea to develop into spheres. These spheres contain Abcg2, Jagged1 and Notch1 positive progenitor cells that can divide and generate new hair cell-like cells, i.e. immunopositive for specific hair cell markers, including Myosin VI, Myosin VIIa, Math1 and ability to uptake FM1-43. We demonstrate that reducing Notch signaling with a gamma secretase inhibitor decreases the number of spheres generated following treatment of the stem/progenitor cell cultures. Additionally, activation of Notch by an exogenous soluble form of a Notch ligand, i.e. Jagged1 protein, promotes sphere formation and the sensory potential of cochlear stem/progenitor cells. Our findings suggest that Notch1/Jagged1 signaling plays a role in maintaining a population of Abcg2 sensory stem/progenitor cells in the postnatal cochlea.

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Year:  2008        PMID: 18571907     DOI: 10.1016/j.mod.2008.05.001

Source DB:  PubMed          Journal:  Mech Dev        ISSN: 0925-4773            Impact factor:   1.882


  15 in total

1.  [Characterization of stem cells derived from the neonatal auditory sensory epithelium].

Authors:  M Diensthuber; S Heller
Journal:  HNO       Date:  2010-11       Impact factor: 1.284

2.  Stem/progenitor cells derived from the cochlear sensory epithelium give rise to spheres with distinct morphologies and features.

Authors:  Marc Diensthuber; Kazuo Oshima; Stefan Heller
Journal:  J Assoc Res Otolaryngol       Date:  2009-02-27

3.  Tympanic border cells are Wnt-responsive and can act as progenitors for postnatal mouse cochlear cells.

Authors:  Taha Adnan Jan; Renjie Chai; Zahra Nabi Sayyid; Renée van Amerongen; Anping Xia; Tian Wang; Saku Tapani Sinkkonen; Yi Arial Zeng; Jared Ruben Levin; Stefan Heller; Roel Nusse; Alan Gi-Lun Cheng
Journal:  Development       Date:  2013-03       Impact factor: 6.868

4.  Isolating LacZ-expressing cells from mouse inner ear tissues using flow cytometry.

Authors:  Taha A Jan; Renjie Chai; Zahra N Sayyid; Alan G Cheng
Journal:  J Vis Exp       Date:  2011-12-23       Impact factor: 1.355

5.  Notch signaling alters sensory or neuronal cell fate specification of inner ear stem cells.

Authors:  Sang-Jun Jeon; Masato Fujioka; Shi-Chan Kim; Albert S B Edge
Journal:  J Neurosci       Date:  2011-06-08       Impact factor: 6.167

Review 6.  Postnatal development, maturation and aging in the mouse cochlea and their effects on hair cell regeneration.

Authors:  Bradley J Walters; Jian Zuo
Journal:  Hear Res       Date:  2012-11-16       Impact factor: 3.208

7.  Notch signaling in mammalian hair cell regeneration.

Authors:  Amber D Slowik; Olivia Bermingham-McDonogh
Journal:  Trends Dev Biol       Date:  2013

8.  Intrinsic regenerative potential of murine cochlear supporting cells.

Authors:  Saku T Sinkkonen; Renjie Chai; Taha A Jan; Byron H Hartman; Roman D Laske; Felix Gahlen; Wera Sinkkonen; Alan G Cheng; Kazuo Oshima; Stefan Heller
Journal:  Sci Rep       Date:  2011-06-29       Impact factor: 4.379

9.  Retention of progenitor cell phenotype in otospheres from guinea pig and mouse cochlea.

Authors:  Jeanne Oiticica; Luiz Carlos M Barboza-Junior; Ana Carla Batissoco; Karina Lezirovitz; Regina C Mingroni-Netto; Luciana A Haddad; Ricardo F Bento
Journal:  J Transl Med       Date:  2010-11-18       Impact factor: 5.531

10.  Spiral ganglion stem cells can be propagated and differentiated into neurons and glia.

Authors:  Marc Diensthuber; Veronika Zecha; Jens Wagenblast; Stefan Arnhold; Albert S B Edge; Timo Stöver
Journal:  Biores Open Access       Date:  2014-06-01
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