Suppr超能文献

声过载刺激可改变耳蜗感觉上皮细胞中 Mcl-1 的表达。

Acoustic overstimulation modifies Mcl-1 expression in cochlear sensory epithelial cells.

机构信息

Center for Hearing and Deafness, State University of New York at Buffalo, Buffalo, New York 14214, USA.

出版信息

J Neurosci Res. 2010 Jun;88(8):1812-21. doi: 10.1002/jnr.22333.

Abstract

Acoustic overstimulation causes apoptotic cell death in the cochlea. This death process is mediated, in part, by the mitochondrial signaling pathway involving Bcl-2 family proteins. Myeloid cell leukemia sequence 1 (Mcl-l) is an antiapoptotic member of the Bcl-2 family. Its involvement in noise-induced hair cell death has not been characterized. Here we report the endogenous expression and the noise-induced expression of Mcl-1 in Sprague Dawley rat cochleae. In the sensory epithelia of normal cochleae, there is strong constitutive expression of Mcl-1 mRNA, with an expression level higher than that of many other Bcl-2 family genes. The Mcl-1 protein is preferentially expressed in outer hair cells. After exposure to a high level of continuous noise at 115-dB sound pressure level for 1 hr, Mcl-1 expression displays a time-dependent alteration, with up-regulation of Mcl-1 mRNA at 4 hr postexposure and protein up-regulation at 1 day postexposure. Western blot analysis reveals the up-regulated Mcl-1 as the full-length form of Mcl-1. Immunolabeling of the Mcl-1 protein reveals the early increase in Mcl-1 immunoreactivity in the nuclear region of the hair cells displaying apoptotic phenotypes and a subsequent increase in survival hair cells. These results suggest that Mcl-1 is involved in the regulation of hair cell pathogenesis resulting from acoustic stress, possibly by influencing the nuclear events of apoptosis.

摘要

声过强刺激会引起耳蜗中的细胞凋亡。这个死亡过程部分是由涉及 Bcl-2 家族蛋白的线粒体信号通路介导的。髓样细胞白血病序列 1(Mcl-1)是 Bcl-2 家族的一种抗凋亡成员。其在噪声诱导的毛细胞死亡中的作用尚未确定。在这里,我们报告了 Sprague Dawley 大鼠耳蜗中 Mcl-1 的内源性表达和噪声诱导表达。在正常耳蜗的感觉上皮中,Mcl-1 mRNA 有强烈的组成型表达,其表达水平高于许多其他 Bcl-2 家族基因。Mcl-1 蛋白在外毛细胞中优先表达。在 115 分贝声压级的连续高声暴露 1 小时后,Mcl-1 表达呈现出时间依赖性变化,暴露后 4 小时 Mcl-1 mRNA 上调,暴露后 1 天蛋白上调。Western blot 分析显示上调的 Mcl-1 为全长形式的 Mcl-1。Mcl-1 蛋白的免疫标记显示,在显示凋亡表型的毛细胞的核区,Mcl-1 免疫反应性早期增加,随后存活的毛细胞增加。这些结果表明,Mcl-1 参与了声应激引起的毛细胞发病机制的调节,可能通过影响凋亡的核事件。

相似文献

1
Acoustic overstimulation modifies Mcl-1 expression in cochlear sensory epithelial cells.
J Neurosci Res. 2010 Jun;88(8):1812-21. doi: 10.1002/jnr.22333.
2
Age-related changes in the ratio of Mcl-1/Bax expression in the rat cochlea.
Acta Otolaryngol. 2012 Feb;132(2):123-32. doi: 10.3109/00016489.2011.631191. Epub 2011 Dec 27.
3
Modulation of Mcl-1 expression reduces age-related cochlear degeneration.
Neurobiol Aging. 2013 Nov;34(11):2647-58. doi: 10.1016/j.neurobiolaging.2013.05.012. Epub 2013 Jun 19.
4
The miR-183/Taok1 target pair is implicated in cochlear responses to acoustic trauma.
PLoS One. 2013;8(3):e58471. doi: 10.1371/journal.pone.0058471. Epub 2013 Mar 5.
6
Transcriptional changes in adhesion-related genes are site-specific during noise-induced cochlear pathogenesis.
Neurobiol Dis. 2012 Feb;45(2):723-32. doi: 10.1016/j.nbd.2011.10.018. Epub 2011 Oct 25.
10
Differential expression of apoptosis-related genes in the cochlea of noise-exposed rats.
Neuroscience. 2009 Jul 7;161(3):915-25. doi: 10.1016/j.neuroscience.2009.03.072. Epub 2009 Apr 5.

引用本文的文献

1
New Insights on the Effect of TNF Alpha Blockade by Gene Silencing in Noise-Induced Hearing Loss.
Int J Mol Sci. 2020 Apr 13;21(8):2692. doi: 10.3390/ijms21082692.
2
Validation of Reference Genes for RT-qPCR Analysis in Noise-Induced Hearing Loss: A Study in Wistar Rat.
PLoS One. 2015 Sep 14;10(9):e0138027. doi: 10.1371/journal.pone.0138027. eCollection 2015.
4
Molecular profile of cochlear immunity in the resident cells of the organ of Corti.
J Neuroinflammation. 2014 Oct 14;11:173. doi: 10.1186/s12974-014-0173-8.
5
Wistar rats: a forgotten model of age-related hearing loss.
Front Aging Neurosci. 2014 Mar 5;6:29. doi: 10.3389/fnagi.2014.00029. eCollection 2014.
6
Modulation of Mcl-1 expression reduces age-related cochlear degeneration.
Neurobiol Aging. 2013 Nov;34(11):2647-58. doi: 10.1016/j.neurobiolaging.2013.05.012. Epub 2013 Jun 19.
7
Transcriptome characterization by RNA-Seq reveals the involvement of the complement components in noise-traumatized rat cochleae.
Neuroscience. 2013 Sep 17;248:1-16. doi: 10.1016/j.neuroscience.2013.05.038. Epub 2013 May 30.
8
The miR-183/Taok1 target pair is implicated in cochlear responses to acoustic trauma.
PLoS One. 2013;8(3):e58471. doi: 10.1371/journal.pone.0058471. Epub 2013 Mar 5.
10
Age-related changes in the ratio of Mcl-1/Bax expression in the rat cochlea.
Acta Otolaryngol. 2012 Feb;132(2):123-32. doi: 10.3109/00016489.2011.631191. Epub 2011 Dec 27.

本文引用的文献

1
Noise induced changes in the expression of p38/MAPK signaling proteins in the sensory epithelium of the inner ear.
J Proteomics. 2011 Dec 21;75(2):410-24. doi: 10.1016/j.jprot.2011.08.007. Epub 2011 Aug 16.
3
Selective vulnerability of the cochlear Basal turn to acrylonitrile and noise.
J Toxicol. 2009;2009:908596. doi: 10.1155/2009/908596. Epub 2009 May 6.
5
L-selectin: role in regulating homeostasis and cutaneous inflammation.
J Dermatol Sci. 2009 Dec;56(3):141-7. doi: 10.1016/j.jdermsci.2009.10.001. Epub 2009 Nov 3.
7
Differential expression of apoptosis-related genes in the cochlea of noise-exposed rats.
Neuroscience. 2009 Jul 7;161(3):915-25. doi: 10.1016/j.neuroscience.2009.03.072. Epub 2009 Apr 5.
8
Gap junctions and connexins in the inner ear: their roles in homeostasis and deafness.
Curr Opin Otolaryngol Head Neck Surg. 2008 Oct;16(5):452-7. doi: 10.1097/MOO.0b013e32830e20b0.
9
Use of Bordetella pertussis BP3385 to establish a cutoff value for an IS481-targeted real-time PCR assay.
J Clin Microbiol. 2008 Nov;46(11):3798-9. doi: 10.1128/JCM.01551-08. Epub 2008 Sep 10.
10
Heterotopic rat heart transplantation (Lewis to F344): early ICAM-1 expression after 8 hours of cold ischemia.
J Heart Lung Transplant. 2008 Sep;27(9):1031-5. doi: 10.1016/j.healun.2008.06.001. Epub 2008 Jul 26.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验