Literature DB >> 19776286

A chimera analysis of prestin knock-out mice.

Mary Ann Cheatham1, Sharon Low-Zeddies, Khurram Naik, Roxanne Edge, Jing Zheng, Charles T Anderson, Peter Dallos.   

Abstract

A chimera is a genetic composite containing a unique mix of cells derived from more than one zygote. This mouse model allows one to learn how cells of contrasting genotype functionally interact in vivo. Here, we investigate the effect that different proportions of prestin-containing outer hair cells (OHC) have on cochlear amplification. To address this issue, we developed a prestin chimeric mouse in which both ROSA26 wild-type (WT) and prestin knock-out (KO) genotypes are present in a single cochlea. The WT ROSA26 mice express a cell marker, allowing one to identify cells originating from the WT genome. Examination of cochlear tissue indicated that prestin chimeric mice demonstrate a mosaic in which mutant and normal OHCs interleave along the cochlear partition, similar to all other chimeric mouse models. The anatomical distribution of prestin-containing OHCs was compared with physiological data including thresholds and tuning curves for the compound action potential (CAP) recorded in anesthetized mice. Analysis of these measures did not reveal mixed phenotypes in which the distribution of prestin-containing OHCs impacted sensitivity and frequency selectivity to different degrees. However, by reducing the number of prestin-containing OHCs, phenotypes intermediate between WT and KO response patterns were obtained. Accordingly, we demonstrate a proportional reduction in sensitivity and in the tip length of CAP tuning curves as the number of OHCs derived from the KO genome increases; i.e., genotype ratio and phenotype are closely related.

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Year:  2009        PMID: 19776286      PMCID: PMC2801582          DOI: 10.1523/JNEUROSCI.1651-09.2009

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  44 in total

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Journal:  Nature       Date:  2000-05-11       Impact factor: 49.962

4.  Disruption of overlapping transcripts in the ROSA beta geo 26 gene trap strain leads to widespread expression of beta-galactosidase in mouse embryos and hematopoietic cells.

Authors:  B P Zambrowicz; A Imamoto; S Fiering; L A Herzenberg; W G Kerr; P Soriano
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-15       Impact factor: 11.205

5.  Cell lineage relationships in the development of the mammalian CNS. II. Bilateral independence of CNS clones.

Authors:  K Herrup; R Wetts; T J Diglio
Journal:  J Neurogenet       Date:  1984-12       Impact factor: 1.250

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Authors:  M L Oster-Granite; J Gearhart
Journal:  Dev Biol       Date:  1981-07-15       Impact factor: 3.582

7.  Neuronal lineages in chimeric mouse forebrain are segregated between compartments and in the rostrocaudal and radial planes.

Authors:  G Fishell; J Rossant; D van der Kooy
Journal:  Dev Biol       Date:  1990-09       Impact factor: 3.582

8.  Cochlear cytogenesis visualized through pulse labeling of chick embryos in culture.

Authors:  A Katayama; J T Corwin
Journal:  J Comp Neurol       Date:  1993-07-01       Impact factor: 3.215

9.  Prestin-based outer hair cell electromotility in knockin mice does not appear to adjust the operating point of a cilia-based amplifier.

Authors:  Jiangang Gao; Xiang Wang; Xudong Wu; Sal Aguinaga; Kristin Huynh; Shuping Jia; Keiji Matsuda; Manish Patel; Jing Zheng; Maryann Cheatham; David Z He; Peter Dallos; Jian Zuo
Journal:  Proc Natl Acad Sci U S A       Date:  2007-07-18       Impact factor: 11.205

10.  Frizzled6 controls hair patterning in mice.

Authors:  Nini Guo; Charles Hawkins; Jeremy Nathans
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-28       Impact factor: 11.205

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  7 in total

Review 1.  Progress in cochlear physiology after Békésy.

Authors:  John J Guinan; Alec Salt; Mary Ann Cheatham
Journal:  Hear Res       Date:  2012-05-23       Impact factor: 3.208

2.  Reduced electromotility of outer hair cells associated with connexin-related forms of deafness: an in silico study of a cochlear network mechanism.

Authors:  Pavel Mistrík; Jonathan F Ashmore
Journal:  J Assoc Res Otolaryngol       Date:  2010-07-16

3.  Normal hearing sensitivity at low-to-middle frequencies with 34% prestin-charge density.

Authors:  Tetsuji Yamashita; Jie Fang; Jiangang Gao; Yiling Yu; Marcia Mellado Lagarde; Jian Zuo
Journal:  PLoS One       Date:  2012-09-21       Impact factor: 3.240

4.  Hearing consequences in Gjb2 knock-in mice: implications for human p.V37I mutation.

Authors:  Xin Lin; Gen Li; Yu Zhang; Jingjing Zhao; Jiawen Lu; Yunge Gao; Huihui Liu; Geng-Lin Li; Tao Yang; Lei Song; Hao Wu
Journal:  Aging (Albany NY)       Date:  2019-09-27       Impact factor: 5.682

5.  Prestin regulation and function in residual outer hair cells after noise-induced hearing loss.

Authors:  Anping Xia; Yohan Song; Rosalie Wang; Simon S Gao; Will Clifton; Patrick Raphael; Sung-il Chao; Fred A Pereira; Andrew K Groves; John S Oghalai
Journal:  PLoS One       Date:  2013-12-20       Impact factor: 3.240

6.  Loss of the Cochlear Amplifier Prestin Reduces Temporal Processing Efficacy in the Central Auditory System.

Authors:  Joseph P Walton; Adam C Dziorny; Olga N Vasilyeva; Anne E Luebke
Journal:  Front Cell Neurosci       Date:  2018-09-21       Impact factor: 5.505

7.  Selective ablation of pillar and deiters' cells severely affects cochlear postnatal development and hearing in mice.

Authors:  Marcia M Mellado Lagarde; Brandon C Cox; Jie Fang; Ruth Taylor; Andrew Forge; Jian Zuo
Journal:  J Neurosci       Date:  2013-01-23       Impact factor: 6.167

  7 in total

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