Literature DB >> 9263030

Immortalized cell lines from embryonic avian and murine otocysts: tools for molecular studies of the developing inner ear.

K F Barald1, K H Lindberg, K Hardiman, A I Kavka, J E Lewis, J C Victor, C A Gardner, A Poniatowski.   

Abstract

Recently, our studies have focused on genes expressed at the earliest stages of inner ear development. Our aim is to identify and characterize genes that are involved in determining the axes of the semicircular canals, in otic crest delamination and in early innervation of the inner ear. Many elegant studies of auditory development have been done in animal models. However, the need for large amounts of well-characterized embryonic material for molecular studies makes the development of otocyst cell lines with different genetic repertoires attractive. We have therefore derived immortalized otocyst cells from two of the most widely used animal models of ear development: avians and mice. Avian cell isolates were produced from quail otocysts (embryonic stage 19) that were transformed with temperature-sensitive variants of the Rous sarcoma virus (RSV). Among the individual transformed cells are those that produce neuron-like derivatives in response to treatment with 10(-9) M retinoic acid. Mammalian cell isolates were derived from otocysts, of 9 day (post coitus) embryos of the H2kbtsA58 transgenic mouse (Immortomouse), which carries a temperature-sensitive variant of the Simian Virus 40 Tumor antigen. The vast majority of cells of the Immortomouse are capable of being immortalized at 33 degrees C, the permissive temperature for transgene expression, in the presence of gamma-interferon. Several putative clones et these cells differentiated into neuron-like cells after temperature shift and withdrawal of gamma-interferon; another isolate of cells assumed a neuron-like morphology on exposure to brain-derived neurotrophic factor even at the permissive temperature. We describe also a cell isolate that expresses the Pax-2 protein product and two putative cell lines that express the protein product of the chicken equivalent of the Drosophila segmentation gene engrailed. These genes and their protein products are expressed in specific subpopulation of otocyst cells at early stages. Both mouse and quail immortalized cell lines will be used to study inner ear development at the molecular level.

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Year:  1997        PMID: 9263030     DOI: 10.1016/s0736-5748(96)00108-6

Source DB:  PubMed          Journal:  Int J Dev Neurosci        ISSN: 0736-5748            Impact factor:   2.457


  12 in total

1.  Differentiation of mammalian vestibular hair cells from conditionally immortal, postnatal supporting cells.

Authors:  P Lawlor; W Marcotti; M N Rivolta; C J Kros; M C Holley
Journal:  J Neurosci       Date:  1999-11-01       Impact factor: 6.167

2.  Immortalized CNS pericytes are quiescent smooth muscle actin-negative and pluripotent.

Authors:  Paula Dore-Duffy; Afroza Mehedi; Xueqian Wang; Michael Bradley; Richard Trotter; Alexander Gow
Journal:  Microvasc Res       Date:  2011-04-15       Impact factor: 3.514

3.  Identification of direct downstream targets of Dlx5 during early inner ear development.

Authors:  Samin A Sajan; John L R Rubenstein; Mark E Warchol; Michael Lovett
Journal:  Hum Mol Genet       Date:  2011-01-12       Impact factor: 6.150

4.  Evolution of periodontal regeneration: from the roots' point of view.

Authors:  M J Somerman; H J Ouyang; J E Berry; N E Saygin; C L Strayhorn; J A D'Errico; T Hullinger; W V Giannobile
Journal:  J Periodontal Res       Date:  1999-10       Impact factor: 4.419

5.  Immortalized mouse inner ear cell lines demonstrate a role for chemokines in promoting the growth of developing statoacoustic ganglion neurons.

Authors:  Lynne M Bianchi; Zeeba Daruwalla; Therese M Roth; Naweah P Attia; Nicholas W Lukacs; Ayo-Lynn Richards; Ian O White; Susan J Allen; Kate F Barald
Journal:  J Assoc Res Otolaryngol       Date:  2005-12

6.  A Gata3 3' Distal Otic Vesicle Enhancer Directs Inner Ear-Specific Gata3 Expression.

Authors:  Takashi Moriguchi; Tomofumi Hoshino; Arvind Rao; Lei Yu; Jun Takai; Satoshi Uemura; Kazue Ise; Yasuhiro Nakamura; Kim-Chew Lim; Ritsuko Shimizu; Masayuki Yamamoto; James Douglas Engel
Journal:  Mol Cell Biol       Date:  2018-10-15       Impact factor: 4.272

7.  Retinoic acid repression of bone morphogenetic protein 4 in inner ear development.

Authors:  Deborah L Thompson; Lisa M Gerlach-Bank; Kate F Barald; Ronald J Koenig
Journal:  Mol Cell Biol       Date:  2003-04       Impact factor: 4.272

Review 8.  Therapeutic potential of neurotrophins for treatment of hearing loss.

Authors:  W Q Gao
Journal:  Mol Neurobiol       Date:  1998       Impact factor: 5.590

Review 9.  Drug screening for hearing loss: using the zebrafish lateral line to screen for drugs that prevent and cause hearing loss.

Authors:  Henry C Ou; Felipe Santos; David W Raible; Julian A Simon; Edwin W Rubel
Journal:  Drug Discov Today       Date:  2010-01-22       Impact factor: 7.851

10.  Macrophage migration inhibitory factor acts as a neurotrophin in the developing inner ear.

Authors:  Lisa M Bank; Lynne M Bianchi; Fumi Ebisu; Dov Lerman-Sinkoff; Elizabeth C Smiley; Yu-chi Shen; Poornapriya Ramamurthy; Deborah L Thompson; Therese M Roth; Christine R Beck; Matthew Flynn; Ryan S Teller; Luming Feng; G Nicholas Llewellyn; Brandon Holmes; Cyrrene Sharples; Jaeda Coutinho-Budd; Stephanie A Linn; Andrew P Chervenak; David F Dolan; Jennifer Benson; Ariane Kanicki; Catherine A Martin; Richard Altschuler; Alisa E Koch; Alicia E Koch; Ethan M Jewett; John A Germiller; Kate F Barald
Journal:  Development       Date:  2012-12       Impact factor: 6.868

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