Modulation of activator protein 1/DNA binding activity by acoustic overstimulation in the guinea-pig cochlea

被引:13
|
作者
Matsunobu, T
Ogita, K
Schacht, J
机构
[1] Univ Michigan, Kresge Hearing Res Inst, Ann Arbor, MI 48109 USA
[2] Keio Univ, Sch Med, Dept Otolaryngol, Shinjuku Ku, Tokyo 1608582, Japan
[3] Setsunan Univ, Dept Pharmacol, Hirakata, Osaka 5730101, Japan
关键词
auditory system; inner ear; noise trauma; transcription factors; immediate early genes;
D O I
10.1016/j.neuroscience.2003.10.022
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Changes in gene expression are part of the homeostatic machinery with which cells respond to external stimuli or assaults. The activity of the early response transcriptional factor activator protein-1 (AP-1) can be modulated by a variety of environmental stimuli including those that alter the cellular oxidation/reduction status. This study investigates the activation of AP-1/DNA binding in the guinea-pig cochlea in response to acoustic overstimulation which produces reactive oxygen species. Electrophoretic mobility shift assays revealed that binding of AP-1 to its radiolabeled oligonucleotide probe markedly changed in nuclear extracts of inner ear tissues following intense noise exposure (4 kHz octave band, 115 dB, 5 h). AP-1/DNA binding increased in the organ of Corti and the lateral wall tissues immediately after the exposure, returning to near-baseline levels 5 h later. At 15 h after noise, a second peak of binding activity occurred in the organ of Corti whereas stria vascularis showed a lesser but more sustained activity. Binding in nuclear extracts from the spiral ganglion did not change. Incubation of nuclear extracts with antibodies against Fos/Jun family proteins prior to a supershift assay showed Fra-2 as a major component of the AP-1 complex immediately after the noise exposure. In the organ of Corti, Fra-2 immunoreactivity was localized to the middle turn, i.e. the region which is most affected by the 4-kHz octave band exposure. The results suggest the modulation of gene expression via the activation of AP-1 as a consequence of noise trauma but also demonstrate differential responses in cochlear tissues. (C) 2004 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1037 / 1043
页数:7
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