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果蝇 TRPA1 通道在味觉受体神经元中介导化学回避。

Drosophila TRPA1 channel mediates chemical avoidance in gustatory receptor neurons.

机构信息

Departmentsof Biological Chemistry and Neuroscience, Center for Sensory Biology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

出版信息

Proc Natl Acad Sci U S A. 2010 May 4;107(18):8440-5. doi: 10.1073/pnas.1001425107. Epub 2010 Apr 19.

Abstract

Mammalian sweet, bitter, and umami taste is mediated by a single transduction pathway that includes a phospholipase C (PLC)beta and one cation channel, TRPM5. However, in insects such as the fruit fly, Drosophila melanogaster, it is unclear whether different tastants, such as bitter compounds, are sensed in gustatory receptor neurons (GRNs) through one or multiple ion channels, as the cation channels required in insect GRNs are unknown. Here, we set out to explore additional sensory roles for the Drosophila TRPA1 channel, which was known to function in thermosensation. We found that TRPA1 was expressed in GRNs that respond to aversive compounds. Elimination of TRPA1 had no impact on the responses to nearly all bitter compounds tested, including caffeine, quinine, and strychnine. Rather, we found that TRPA1 was required in a subset of avoidance GRNs for the behavioral and electrophysiological responses to aristolochic acid. TRPA1 did not appear to be activated or inhibited directly by aristolochic acid. We found that elimination of the same PLC that leads to activation of TRPA1 in thermosensory neurons was also required in the TRPA1-expressing GRNs for avoiding aristolochic acid. Given that mammalian TRPA1 is required for responding to noxious chemicals, many of which cause pain and injury, our analysis underscores the evolutionarily conserved role for TRPA1 channels in chemical avoidance.

摘要

哺乳动物的甜味、苦味和鲜味由单一的转导途径介导,该途径包括磷脂酶 C (PLC)β 和一个阳离子通道,TRPM5。然而,在果蝇等昆虫中,尚不清楚不同的味觉物质,如苦味化合物,是否通过一个或多个阳离子通道在味觉受体神经元 (GRNs) 中被感知,因为昆虫 GRNs 所需的阳离子通道尚不清楚。在这里,我们着手探索果蝇 TRPA1 通道的其他感觉作用,该通道已知在热敏性中起作用。我们发现 TRPA1 在对厌恶化合物有反应的 GRNs 中表达。消除 TRPA1 对测试的几乎所有苦味化合物(包括咖啡因、奎宁和士的宁)的反应没有影响。相反,我们发现 TRPA1 在回避 GRNs 的亚群中对马兜铃酸的行为和电生理反应是必需的。TRPA1 似乎没有被马兜铃酸直接激活或抑制。我们发现,导致热敏神经元中 TRPA1 激活的相同 PLC 的消除对于 TRPA1 表达的 GRNs 中对马兜铃酸的回避也是必需的。鉴于哺乳动物 TRPA1 对有害化学物质的反应是必需的,其中许多化学物质会引起疼痛和伤害,我们的分析强调了 TRPA1 通道在化学回避中的进化保守作用。

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