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嗅觉纤毛:连接感觉纤毛功能与人类疾病

Olfactory cilia: linking sensory cilia function and human disease.

作者信息

Jenkins Paul M, McEwen Dyke P, Martens Jeffrey R

机构信息

Department of Pharmacology, University of Michigan, 1301 MSRB III, Ann Arbor, MI 48109-5632, USA.

出版信息

Chem Senses. 2009 Jun;34(5):451-64. doi: 10.1093/chemse/bjp020. Epub 2009 Apr 30.

Abstract

The olfactory system gives us an awareness of our immediate environment by allowing us to detect airborne stimuli. The components necessary for detection of these odorants are compartmentalized in the cilia of olfactory sensory neurons. Cilia are microtubule-based organelles, which can be found projecting from the surface of almost any mammalian cell, and are critical for proper olfactory function. Mislocalization of ciliary proteins and/or the loss of cilia cause impaired olfactory function, which is now recognized as a clinical manifestation of a broad class of human diseases, termed ciliopathies. Future work investigating the mechanisms of olfactory cilia function will provide us important new information regarding the pathogenesis of human sensory perception diseases.

摘要

嗅觉系统通过让我们检测空气中的刺激物,使我们能够感知周围的环境。检测这些气味分子所需的成分被分隔在嗅觉感觉神经元的纤毛中。纤毛是以微管为基础的细胞器,几乎可以在任何哺乳动物细胞表面伸出,对正常的嗅觉功能至关重要。纤毛蛋白的错误定位和/或纤毛的丧失会导致嗅觉功能受损,现在这被认为是一大类人类疾病(称为纤毛病)的临床表现。未来研究嗅觉纤毛功能机制的工作将为我们提供有关人类感官知觉疾病发病机制的重要新信息。

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本文引用的文献

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OLFACTORY CILIA IN THE FROG.青蛙的嗅觉纤毛。
J Cell Biol. 1965 May 1;25(2):209-30. doi: 10.1083/jcb.25.2.209.
4
The proteome of rat olfactory sensory cilia.大鼠嗅觉感觉纤毛的蛋白质组
Proteomics. 2009 Jan;9(2):322-34. doi: 10.1002/pmic.200800149.
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Ciliary syndromes and treatment.纤毛综合征与治疗
Pathol Res Pract. 2008;204(2):77-88. doi: 10.1016/j.prp.2007.10.013.

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