Literature DB >> 10562438

Establishment and characterization of conditionally immortalized organ of corti cell lines.

F Kalinec1, G Kalinec, M Boukhvalova, B Kachar.   

Abstract

A culture of cells was isolated from the organ of Corti of 2-week-old H-2Kb-tsA58 (Immortomouse) transgenic mice. All cells of these mice harbor a mutant of the simian virus 40 A-gene, encoding a thermolabile large T-antigen (Tag) protein. At 33 degrees C the Tag protein is functional and induces cell proliferation, but at 39 degrees C it is rapidly denatured and inactivated. Isolated organ of Corti cells growing at 33 degrees C were predominantly small, rounded or fusiform and proliferated rapidly. When moved to 39 degrees C, the cells reduced their rate of proliferation and differentiated into specific morphological phenotypes. Four cell lines were cloned by limiting dilution and characterized by immunofluorescence microscopy and Western blot. The cell lines, named OC-k1, OC-k2, OC-k3 and OC-k4, have been passaged at least 50 times with retention of a stable phenotype. These cell lines were all positive for the neuroepithelial precursor cell marker nestin and for the inner ear cell marker OCP2. In addition, the cells showed reactivity to epithelial and neuronal cell markers, but with a pattern of protein expression different for each clone and different between cells of the same clone growing at 33 degrees C or 39 degrees C. Some of the clones exhibited asymmetric cell division which is a characteristic commonly ascribed to stem cells. These cell lines can be used advantageously to study mechanisms and signals involved in the control of cell differentiation and morphogenesis of the mammalian inner ear and to isolate inner ear specific proteins. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10562438     DOI: 10.1006/cbir.1998.0339

Source DB:  PubMed          Journal:  Cell Biol Int        ISSN: 1065-6995            Impact factor:   3.612


  12 in total

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3.  Corticotropin-releasing factor-2 activation prevents gentamicin-induced oxidative stress in cells derived from the inner ear.

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4.  Protective effect of acetyl-l-carnitine against cisplatin ototoxicity: role of apoptosis-related genes and pro-inflammatory cytokines.

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5.  Ototoxicity from combined Cisplatin and radiation treatment: an in vitro study.

Authors:  Wong-Kein Low; Sylvia W W Kong; Michelle G K Tan
Journal:  Int J Otolaryngol       Date:  2010-12-01

Review 6.  Drug screening for hearing loss: using the zebrafish lateral line to screen for drugs that prevent and cause hearing loss.

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7.  Directed differentiation of mouse cochlear neural progenitors in vitro.

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9.  Sox2 in the differentiation of cochlear progenitor cells.

Authors:  Judith S Kempfle; Jack L Turban; Albert S B Edge
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10.  Pharmacogenetic variants in TPMT alter cellular responses to cisplatin in inner ear cell lines.

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Journal:  PLoS One       Date:  2017-04-13       Impact factor: 3.240

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