首页> 美国卫生研究院文献>Frontiers in Systems Neuroscience >Tyramine Actions on Drosophila Flight Behavior Are Affected by a Glial Dehydrogenase/Reductase
【2h】

Tyramine Actions on Drosophila Flight Behavior Are Affected by a Glial Dehydrogenase/Reductase

机译:酪胺对果蝇飞行行为的作用受胶质脱氢酶/还原酶的影响。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The biogenic amines octopamine (OA) and tyramine (TA) modulate insect motor behavior in an antagonistic manner. OA generally enhances locomotor behaviors such as Drosophila larval crawling and flight, whereas TA decreases locomotor activity. However, the mechanisms and cellular targets of TA modulation of locomotor activity are incompletely understood. This study combines immunocytochemistry, genetics and flight behavioral assays in the Drosophila model system to test the role of a candidate enzyme for TA catabolism, named Nazgul (Naz), in flight motor behavioral control. We hypothesize that the dehydrogenase/reductase Naz represents a critical step in TA catabolism. Immunocytochemistry reveals that Naz is localized to a subset of Repo positive glial cells with cell bodies along the motor neuropil borders and numerous positive Naz arborizations extending into the synaptic flight motor neuropil. RNAi knock down of Naz in Repo positive glial cells reduces Naz protein level below detection level by Western blotting. The resulting consequence is a reduction in flight durations, thus mimicking known motor behavioral phenotypes as resulting from increased TA levels. In accord with the interpretation that reduced TA degradation by Naz results in increased TA levels in the flight motor neuropil, the motor behavioral phenotype can be rescued by blocking TA receptors. Our findings indicate that TA modulates flight motor behavior by acting on central circuitry and that TA is normally taken up from the central motor neuropil by Repo-positive glial cells, desaminated and further degraded by Naz.
机译:生物胺章鱼胺(OA)和酪胺(TA)以拮抗方式调节昆虫的运动行为。 OA通常会增强运动行为,例如果蝇幼虫的爬行和飞行,而TA会降低运动活性。但是,尚未完全了解运动调节活性的TA调节机制和细胞靶标。这项研究结合了果蝇模型系统中的免疫细胞化学,遗传学和飞行行为分析,以测试名为Nazgul(Naz)的TA分解代谢候选酶在飞行运动行为控制中的作用。我们假设脱氢酶/还原酶Naz代表TA分解代谢的关键步骤。免疫细胞化学显示,Naz定位于Repo阳性神经胶质细胞的一个子集,其细胞体沿运动神经pil边界分布,并且许多阳性的Naz树突延伸到突触飞行运动神经pil。 RNAi敲除Repo阳性神经胶质细胞中的Naz,可通过Western印迹将Naz蛋白水平降低到检测水平以下。结果导致飞行时间的减少,从而模仿了由于增加的TA水平而导致的已知运动行为表型。与Naz减少TA降解导致飞行运动神经纤维中TA水平升高的解释一致,可以通过阻断TA受体来挽救运动行为表型。我们的发现表明,TA通过作用于中央电路来调节飞行运动行为,TA通常由正阳性神经胶质细胞从中央运动神经纤维中吸收,并被Naz脱去并进一步降解。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号