DYSGENESIS OF MELANOCYTES AND COCHLEAR DYSFUNCTION IN MUTANT MICROPHTHALMIA (MI) MICE

Citation
H. Motohashi et al., DYSGENESIS OF MELANOCYTES AND COCHLEAR DYSFUNCTION IN MUTANT MICROPHTHALMIA (MI) MICE, Hearing research, 80(1), 1994, pp. 10-20
Citations number
44
Categorie Soggetti
Neurosciences,Acoustics
Journal title
ISSN journal
03785955
Volume
80
Issue
1
Year of publication
1994
Pages
10 - 20
Database
ISI
SICI code
0378-5955(1994)80:1<10:DOMACD>2.0.ZU;2-U
Abstract
In order to evaluate the cytological homology of intermediate cells an d melanocytes, and to investigate the function of melanocytes in the i nner ear, hearing acuity and cochlear pathology were studied in three strains of mice, namely, wild type mice (+/+), albino mice without mel anin (c(2J)/c(2J)) and microphthalmia mice with no melanocytes (mi(bw) /mi(bw)). Our histochemical data indicated that intermediate cells sho wed cytological characteristics almost identical to those of melanocyt es and that disorders of melanin and/or melanocytes were reflected in the stria vascularis of each mouse. While c(2J)/c(2J) presented the sa me normal hearing acuity and normal structure of the stria vascularis as +/+, the hearing acuity of mi(bw)/mi(bw) mutants was severely impai red. Their stria vascularis was abnormally thin, lacking intermediate cells. According to these results, lack of melanin has little influenc e on hearing acuity; however, the absence of intermediate cells or mel anocytes causes severe hearing loss, presumably due to a strial dysfun ction.