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痕量胺相关受体:配体、神经回路及行为

Trace amine-associated receptors: ligands, neural circuits, and behaviors.

作者信息

Liberles Stephen D

机构信息

Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Curr Opin Neurobiol. 2015 Oct;34:1-7. doi: 10.1016/j.conb.2015.01.001. Epub 2015 Jan 20.

Abstract

Trace amine-associated receptors (TAARs) are G Protein-Coupled Receptors that function as vertebrate olfactory receptors. Like odorant receptors, TAARs constitute an ever-evolving sensory subsystem, with individual TAARs recognizing particular chemicals and some evoking stereotyped behaviors. Several TAARs mediate aversion or attraction towards volatile amines that include the mouse odor trimethylamine, the predator odor 2-phenylethylamine, and the death-associated odor cadaverine. TAAR-expressing sensory neurons achieve monoallelic receptor expression, use canonical olfactory signaling molecules, and target a dedicated olfactory bulb region. In mouse, TAAR4 and TAAR5 are encoded by adjacent genes and localize to adjacent glomeruli, yet mediate opposing behaviors. Future studies are needed to understand how TAAR-expressing sensory neurons engage higher-order neural circuits to encode odor valence.

摘要

痕量胺相关受体(TAARs)是作为脊椎动物嗅觉受体发挥作用的G蛋白偶联受体。与气味受体一样,TAARs构成了一个不断进化的感觉子系统,其中单个TAARs识别特定化学物质,有些还会引发刻板行为。几种TAARs介导对挥发性胺的厌恶或吸引,这些挥发性胺包括小鼠气味三甲胺、捕食者气味2-苯乙胺和与死亡相关的气味尸胺。表达TAAR的感觉神经元实现单等位基因受体表达,使用经典嗅觉信号分子,并靶向专门的嗅球区域。在小鼠中,TAAR4和TAAR5由相邻基因编码并定位于相邻的肾小球,但介导相反的行为。未来需要开展研究以了解表达TAAR的感觉神经元如何参与高阶神经回路来编码气味效价。

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本文引用的文献

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Aversion and attraction through olfaction.通过嗅觉产生的厌恶与吸引。
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Olfactory receptor patterning in a higher primate.一种高等灵长类动物的嗅觉受体模式形成
J Neurosci. 2014 Sep 10;34(37):12241-52. doi: 10.1523/JNEUROSCI.1779-14.2014.
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High-affinity olfactory receptor for the death-associated odor cadaverine.高亲和力嗅觉受体对与死亡相关的气味尸胺。
Proc Natl Acad Sci U S A. 2013 Nov 26;110(48):19579-84. doi: 10.1073/pnas.1318596110. Epub 2013 Nov 11.
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Mammalian pheromones.哺乳动物信息素。
Annu Rev Physiol. 2014;76:151-75. doi: 10.1146/annurev-physiol-021113-170334. Epub 2013 Aug 26.

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