电压门控离子通道TRP/ pain - less调节鳞翅目幼虫马氏小管的排泄功能。

IF 2.8 2区 生物学 Q2 BIOLOGY
Jocelyne Dates, Alexis Castaneda, Serena Farrell, Nancy Ramirez, Dennis Kolosov
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引用次数: 0

摘要

鳞翅目幼虫是一种食性强、生长迅速的农业害虫,需要一个高效的排泄系统,由功能相当于人类肾脏的马尔比氏小管(MTs)和后肠组成。鳞翅类幼虫的MTs远端嵌入一种称为直肠复体的特殊器官中,能够从饮食中提取离子和水,从而驱动其MTs中的液体分泌和排泄。毛虫MTs的一个独特特征是,它们可以快速(约10分钟)在使用血淋巴离子和饮食离子之间切换,以在面对不断变化的饮食离子供应时保持恒定的液体分泌。先前的转录组学研究表明,电压门控离子通道(vgic)在白菜环虫(Trichoplusia ni)幼虫的MTs中表达,为实现这种快速离子转运开关的机制之一提供了基础。在本研究中,我们证明了Ca2+渗透性TRP/Painless(以及其他VGICs)在毛虫、家蚕、雌雄蛾、小菜蛾和frugiperda幼虫的DIP中表达。在T. ni幼虫中,我们发现TRP/Painless存在于远端回肠丛(DIP)的次级细胞中,其mRNA丰度在分泌DIP时更高。此外,药物抑制TRP/Painless可降低经上皮膜电位、主细胞K+转运和液体分泌速率,而TRP/Painless激活则相反。我们的数据表明,TRP/无痛调节鳞翅目mtts上皮中的离子运输。这项工作可能为未来针对鳞翅目幼虫的综合害虫管理策略提供目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Voltage-gated ion channel TRP/Painless regulates the excretory function of the Malpighian tubules in larval lepidopterans.

Lepidopteran larvae are agricultural pests that feed voraciously and grow rapidly, requiring an efficient excretory system, consisting of a combo functionally equivalent to the human kidney - Malpighian tubules (MTs) and hindgut. In larval lepidopterans, distal ends of MTs are embedded into a specialized organ termed rectal complex, enabling dietary extraction of ions and water, which drives fluid secretion and excretion in their MTs. A unique feature of caterpillar MTs is that they can rapidly (∼10 min) switch between using haemolymph ions and dietary ions to maintain constant fluid secretion in the face of changing dietary ion availability. Previous transcriptomic studies suggested that voltage-gated ion channels (VGICs) are expressed in the MTs of the larval cabbage looper Trichoplusia ni, providing the basis for one of the mechanisms enabling this rapid ion transport switch. In the current study, we demonstrate that Ca2+-permeable TRP/Painless (and other VGICs) are expressed in the DIP of Trichoplusia ni, Bombyx mori, Manduca sexta, Plutella xylostella, and Spodoptera frugiperda larvae. In larval T. ni, we demonstrate that TRP/Painless is found in the secondary cells of the distal ileac plexus (DIP) and its mRNA abundance is higher in secreting DIP. Moreover, pharmacological inhibition of TRP/Painless reduces transepithelial membrane potential, K+ transport by principal cells, and fluid secretion rate, while TRP/Painless activation does the opposite. Our data demonstrate that TRP/Painless regulates ion transport in epithelia of lepidopteran MTs. This work may provide targets for future integrated pest management strategies aimed specifically at lepidopteran larvae in the agricultural setting.

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来源期刊
CiteScore
5.50
自引率
10.70%
发文量
494
审稿时长
1 months
期刊介绍: Journal of Experimental Biology is the leading primary research journal in comparative physiology and publishes papers on the form and function of living organisms at all levels of biological organisation, from the molecular and subcellular to the integrated whole animal.
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