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通过免疫定位和RNA干扰(RNAi)阐明曼氏血吸虫中5-羟色胺转运体的功能作用。

The functional role of a serotonin transporter in Schistosoma mansoni elucidated through immunolocalization and RNA interference (RNAi).

作者信息

Patocka Nicholas, Ribeiro Paula

机构信息

Institute of Parasitology, McGill University, Macdonald Campus, 21, Ste-Anne-de-Bellevue, Quebec, Canada H9X 3V9.

出版信息

Mol Biochem Parasitol. 2013 Jan;187(1):32-42. doi: 10.1016/j.molbiopara.2012.11.008. Epub 2012 Dec 14.

Abstract

Serotonin is an important neurotransmitter in both vertebrates and invertebrates. In the parasitic flatworm, Schistosoma mansoni, serotonin stimulates worm movement and potentiates muscle contraction. A specific serotonin transporter (SmSERT) was previously cloned from S. mansoni and characterized in vitro. Here we conduct a first investigation of the native protein in the worm so as to elucidate the biological role of SmSERT and to assess its drug targeting potential. Confocal immunofluorescence studies using specific antibodies determined that SmSERT is expressed predominantly in the nervous system both in adult worms and larvae (schistosomula). SmSERT immunoreactivity was detected in the main nerve cords of the central nervous system and the peripheral nerve plexus of the body wall in adult males and females, in apparent nerve endings of the male tubercles and possibly the male tegument. In the larvae, SmSERT localized mainly to the peripheral nerve plexus of the body wall. Co-localization experiments showed that the pattern of SmSERT expression coincides with that of serotonin itself, suggesting that SmSERT is present in serotonergic neurons. To test whether SmSERT is involved in the motor effects of serotonin, we treated S. mansoni schistosomula with SmSERT blockers or SmSERT-specific short-interfering RNAs (siRNAs) and then recorded larval motility, using a quantitative imaging assay. In both cases, the treatment produced a strongly hyperactive phenotype, corresponding to a 3-fold increase in larval motility, roughly the same effect as treatment with an excess of exogenous serotonin. The siRNA effect correlated with a ≈50% decrease in expression of the SmSERT when tested by real-time qPCR. To test if SmSERT mediates transport of exogenous serotonin across the tegument, uptake assays were also performed in intact schistosomula treated with SmSERT siRNAs or an irrelevant siRNA. We found a significant but modest decrease (25%) in serotonin uptake in the siRNA-suppressed larvae when compared to the negative controls. These results suggest that the SmSERT's function is primarily neuromuscular and may also play a secondary role in the uptake of exogenous (host-derived) serotonin.

摘要

血清素是脊椎动物和无脊椎动物体内一种重要的神经递质。在寄生扁虫曼氏血吸虫中,血清素可刺激虫体运动并增强肌肉收缩。此前已从曼氏血吸虫中克隆出一种特定的血清素转运体(SmSERT)并在体外进行了表征。在此,我们首次对该蠕虫体内的天然蛋白进行研究,以阐明SmSERT的生物学作用并评估其作为药物靶点的潜力。使用特异性抗体进行的共聚焦免疫荧光研究确定,SmSERT在成虫和幼虫(血吸虫幼虫)的神经系统中均主要表达。在成年雄性和雌性的中枢神经系统主要神经索以及体壁的外周神经丛中检测到SmSERT免疫反应性,在雄性结节的明显神经末梢以及可能的雄性体表中也检测到。在幼虫中,SmSERT主要定位于体壁的外周神经丛。共定位实验表明,SmSERT的表达模式与血清素本身的模式一致,这表明SmSERT存在于血清素能神经元中。为了测试SmSERT是否参与血清素的运动效应,我们用SmSERT阻滞剂或SmSERT特异性短干扰RNA(siRNA)处理曼氏血吸虫幼虫,然后使用定量成像测定法记录幼虫的运动能力。在这两种情况下,处理均产生了强烈的多动表型,对应于幼虫运动能力增加约3倍,与用过量外源性血清素处理的效果大致相同。通过实时定量PCR检测,siRNA的作用与SmSERT表达降低约50%相关。为了测试SmSERT是否介导外源性血清素跨体表的转运,还在用SmSERT siRNA或无关siRNA处理的完整血吸虫幼虫中进行了摄取测定。我们发现,与阴性对照相比,siRNA抑制的幼虫中血清素摄取有显著但适度的降低(约25%)。这些结果表明,SmSERT的功能主要是神经肌肉性的,也可能在外源性(宿主来源)血清素的摄取中起次要作用。

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