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Drosophila Nociceptors Mediate Larval Aversion to Dry Surface Environments Utilizing Both the Painless TRP Channel and the DEG/ENaC Subunit, PPK1

机译:果蝇伤害感受器通过无痛的TRP通道和DEG / ENaC亚基PPK1介导幼虫对干燥表面环境的厌恶。

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摘要

A subset of sensory neurons embedded within the Drosophila larval body wall have been characterized as high-threshold polymodal nociceptors capable of responding to noxious heat and noxious mechanical stimulation. They are also sensitized by UV-induced tissue damage leading to both thermal hyperalgesia and allodynia very similar to that observed in vertebrate nociceptors. We show that the class IV multiple-dendritic(mdIV) nociceptors are also required for a normal larval aversion to locomotion on to a dry surface environment. Drosophila melanogaster larvae are acutely susceptible to desiccation displaying a strong aversion to locomotion on dry surfaces severely limiting the distance of movement away from a moist food source. Transgenic inactivation of mdIV nociceptor neurons resulted in larvae moving inappropriately into regions of low humidity at the top of the vial reflected as an increased overall pupation height and larval desiccation. This larval lethal desiccation phenotype was not observed in wild-type controls and was completely suppressed by growth in conditions of high humidity. Transgenic hyperactivation of mdIV nociceptors caused a reciprocal hypersensitivity to dry surfaces resulting in drastically decreased pupation height but did not induce the writhing nocifensive response previously associated with mdIV nociceptor activation by noxious heat or harsh mechanical stimuli. Larvae carrying mutations in either the Drosophila TRP channel, Painless, or the degenerin/epithelial sodium channel subunit Pickpocket1(PPK1), both expressed in mdIV nociceptors, showed the same inappropriate increased pupation height and lethal desiccation observed with mdIV nociceptor inactivation. Larval aversion to dry surfaces appears to utilize the same or overlapping sensory transduction pathways activated by noxious heat and harsh mechanical stimulation but with strikingly different sensitivities and disparate physiological responses.
机译:果蝇幼虫体壁内嵌入的感觉神经元的子集已被表征为能够响应有害热量和有害机械刺激的高阈值多峰伤害感受器。它们还被紫外线诱导的组织损伤所致,导致热痛觉过敏和异常性疼痛,这与脊椎动物伤害感受器中观察到的非常相似。我们表明,类IV多树突状(mdIV)伤害感受器也需要正常的幼虫厌恶运动到干燥的表面环境。果蝇的幼虫极易干燥,对干燥表面的运动表现出强烈的反感,严重限制了远离潮湿食物源的运动距离。 mdIV伤害感受器神经元的转基因失活导致幼虫不适当地进入小瓶顶部的低湿度区域,这反映为整体化up高度和幼虫干燥增加。在野生型对照中未观察到这种幼虫致死的干燥表型,并在高湿度条件下被生长完全抑制。 mdIV伤害感受器的转基因超活化导致对干燥表面的相互超敏反应,导致化ation高度急剧降低,但并未诱导以前与有毒热或刺激性机械刺激引起的mdIV伤害感受器活化相关的扭曲的伤害反应。果蝇TRP通道,无痛或简并蛋白/上皮钠通道亚基Pickpocket1(PPK1)中携带突变的幼虫,均在mdIV伤害感受器中表达,显示出相同的不适当的化ation高度增加和mdIV伤害感受器失活观察到的致命干燥。幼虫对干燥表面的厌恶似乎利用了有毒的热和苛刻的机械刺激激活的相同或重叠的感官转导途径,但敏感性和完全不同的生理反应却截然不同。

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