Find-Health-Articles.com - making medical research available to everyone
Research article summary (published 21 Sep 2009):

A chimera analysis of prestin knock-out mice.

Full 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.

 

Author information

Author/s: Cheatham, Mary Ann (MA); Low-Zeddies, Sharon (S); Naik, Khurram (K); Edge, Roxanne (R); Zheng, Jing (J); Anderson, Charles T (CT); Dallos, Peter (P);

Affiliation: Departments of Communication Sciences and Disorders, The Hugh Knowles Center, Northwestern University, Evanston, Illinois 60208, USA. m-cheatham(-atsign-)northwestern.edu

Grants: 5R44MH066670 (Agency:NIMH NIH HHS) ; DC00089 (Agency:NIDCD NIH HHS)

Journal and publication information

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience (J Neurosci), published in United States. (Language: eng)

Reference: 2009-Sep; vol 29 (issue 38) : pp 12000-8

Dates: Created 2009/09/24; Completed 2009/10/09;

PMID: 19776286, status: MEDLINE (last retrieved date: 10/9/2009)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

External Links for this article
(including full text providers, if available):

Click Electronic Full-text Provider Links to see options for finding the electronic full text links to this article. Note there may be a subscription or fee required for access to the full text. See our FAQ for information on finding FREE full text articles.

This article may also be located in paper journal collections available in many libraries. Use the Journal and Publication Information above to find the full article.

MeSH headings (categories)

This article was linked to the MeSH Headings (categories) shown below.

Note: Bold headings indicate primary MeSH headings or qualifiers.

Associated Chemicals: Molecular Motor Proteins (0) ; Pres protein, mouse (0)

Related articles

These are the most related articles currently in our database:

See 100+ related articles.

Related Article Map

6/29/1994
5/6/2008
Higher Relevance Score (100)
Lower Relevance Score (68)

Legend: - FREE Full text Article. - Abstract only. - Title only. More help.

See a larger map of 100+ related articles.

© Advanogy LLC 2003-2010 - All rights reserved. Terms of Use | Contact Us | Index