2009 Fiscal Year Final Research Report
Postnatal Developmental Expression in Gjb2 Transgenic Mice of the Organ of Corti
Project/Area Number |
20890219
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Research Category |
Grant-in-Aid for Young Scientists (Start-up)
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Allocation Type | Single-year Grants |
Research Field |
Otorhinolaryngology
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Research Institution | Juntendo University |
Principal Investigator |
INOSHITA Ayako Juntendo University, 医学部, 助教 (00514762)
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Project Period (FY) |
2008 – 2009
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Keywords | GJB2遺伝子変異 / コネキシン26 / 先天性難聴 / コルチ器 / アポトーシス |
Research Abstract |
A strikingly high proportion of congenital bilateral nonsyndromic sensorineural deafness cases among Japanese have been linked to mutations in the GJB2 coding for the connexin26. We aimed to evaluate the postnatal development of the organ of Corti in GJB2 mutations model mice. The mice showed incomplete development of the cochlear pillar cells and delayed apoptosis in GER. The present findings contribute strongly to one of basic remedies for the congenital deafness caused by Gjb2 mutation.
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[Journal Article] Cochlear outer hair cells in a dominant-negative connexin26 mutant mouse preserve non-linear capacitance in spite of impaired distortion product otoacoustic emission2009
Author(s)
A. MINEKAWA, T. ABE, A. INOSHITA, T. IIZUKA, S. KAKEHATA, Y. NARUI, T. KOIKE, K. KAMIYA, H. OKAMURA, H. SHINKAWA, K. IKEDA
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Journal Title
Neuroscience 164
Pages: 1312-1319
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