Yamashita Daisuke, Minami Shujiro B, Kanzaki Sho, Ogawa Kaoru, Miller Josef M
Kresge Hearing Research Institute, University of Michigan, Ann Arbor, Michigan 48109-0506, USA.
J Neurosci Res. 2008 Mar;86(4):920-8. doi: 10.1002/jnr.21533.
Proteins of the Bcl-2 family have been implicated in control of apoptotic pathways modulating neuronal cell death, including noise-induced hearing loss. In this study, we assessed the expressions of anti- and proapoptotic Bcl-2 genes, represented by Bcl-xL and Bak following noise exposures, which yielded temporary threshold shift (TTS) or permanent threshold shift (PTS). Auditory brainstem responses (ABRs) were assessed at 4, 8, and 16 kHz before exposure and on days 1, 3, 7, and 10 following exposure to 100 dB SPL, 4 kHz OBN, 1 hr (TTS) or 120 dB SPL, 4 kHz OBN, 5 hr (PTS). On day 10, subjects were euthanized. ABR thresholds increased following both exposures, fully recovered following the TTS exposure, and showed a 22.6 dB (4 kHz), 42.5 dB (8 kHz), and 44.9 dB (16 kHz) mean shift on day 10 following the PTS exposure. PTS was accompanied by outer hair cell loss progressing epically and basally from the 4-kHz region. Additional animals were euthanized for immunohistochemical assessment. BcL-xL was robustly expressed in outer hair cells following TTS exposure, whereas Bak was expressed following PTS exposure. These results indicate an important role of the Bcl-2 family proteins in regulating sensory cell survival or death following intense noise. Bcl-xL plays an essential role in prevention of sensory cell death following TTS levels of noise, and PTS exposure provokes the expression of Bak and, with that, cell death.
Bcl-2家族蛋白与调控凋亡途径有关,这些途径可调节神经元细胞死亡,包括噪声性听力损失。在本研究中,我们评估了噪声暴露后抗凋亡和促凋亡Bcl-2基因(以Bcl-xL和Bak为代表)的表达,这些噪声暴露导致了暂时性阈移(TTS)或永久性阈移(PTS)。在暴露前以及暴露于100 dB SPL、4 kHz窄带噪声、1小时(TTS)或120 dB SPL、4 kHz窄带噪声、5小时(PTS)后的第1、3、7和10天,分别在4、8和16 kHz频率评估听觉脑干反应(ABR)。在第10天,对实验对象实施安乐死。两种暴露后ABR阈值均升高,TTS暴露后阈值完全恢复,而PTS暴露后在第10天平均阈值分别在4 kHz处偏移22.6 dB、8 kHz处偏移42.5 dB、16 kHz处偏移44.9 dB。PTS伴有外毛细胞损失,从4 kHz区域开始向顶部和底部发展。另外处死一些动物用于免疫组织化学评估。TTS暴露后BcL-xL在外毛细胞中强烈表达,而PTS暴露后Bak表达。这些结果表明Bcl-2家族蛋白在调节强噪声后感觉细胞的存活或死亡中起重要作用。Bcl-xL在预防TTS水平噪声后的感觉细胞死亡中起关键作用,而PTS暴露会引发Bak的表达,进而导致细胞死亡。