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Signaling of Pigment-Dispersing Factor (PDF) in the Madeira Cockroach Rhyparobia maderae

机译:马德拉蟑螂Rhyparobia maderae中的色素分散因子(PDF)信号

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摘要

The insect neuropeptide pigment-dispersing factor (PDF) is a functional ortholog of vasoactive intestinal polypeptide, the coupling factor of the mammalian circadian pacemaker. Despite of PDF's importance for synchronized circadian locomotor activity rhythms its signaling is not well understood. We studied PDF signaling in primary cell cultures of the accessory medulla, the circadian pacemaker of the Madeira cockroach. In Ca2+ imaging studies four types of PDF-responses were distinguished. In regularly bursting type 1 pacemakers PDF application resulted in dose-dependent long-lasting increases in Ca2+ baseline concentration and frequency of oscillating Ca2+ transients. Adenylyl cyclase antagonists prevented PDF-responses in type 1 cells, indicating that PDF signaled via elevation of intracellular cAMP levels. In contrast, in type 2 pacemakers PDF transiently raised intracellular Ca2+ levels even after blocking adenylyl cyclase activity. In patch clamp experiments the previously characterized types 1–4 could not be identified. Instead, PDF-responses were categorized according to ion channels affected. Application of PDF inhibited outward potassium or inward sodium currents, sometimes in the same neuron. In a comparison of Ca2+ imaging and patch clamp experiments we hypothesized that in type 1 cells PDF-dependent rises in cAMP concentrations block primarily outward K+ currents. Possibly, this PDF-dependent depolarization underlies PDF-dependent phase advances of pacemakers. Finally, we propose that PDF-dependent concomitant modulation of K+ and Na+ channels in coupled pacemakers causes ultradian membrane potential oscillations as prerequisite to efficient synchronization via resonance.
机译:昆虫神经肽色素分散因子(PDF)是血管活性肠多肽(哺乳动物昼夜节律起搏器的耦合因子)的功能直系同源物。尽管PDF对于同步的昼夜运动活动节律很重要,但其信号传导尚不清楚。我们研究了辅助髓质(马德拉蟑螂的昼夜节律起搏器)的原代细胞培养物中的PDF信号传导。在Ca 2 + 成像研究中,区分了四种类型的PDF响应。在定期爆裂的1型起搏器中,PDF应用导致Ca 2 + 基线浓度和Ca 2 + 瞬态振荡频率的剂量依赖性长期增加。腺苷酸环化酶拮抗剂可防止1型细胞发生PDF应答,表明PDF通过升高细胞内cAMP水平发出信号。相反,在2型起搏器中,即使阻断了腺苷酸环化酶的活性,PDF也会暂时升高细胞内Ca 2 + 的水平。在膜片钳实验中,无法确定先前表征的类型1-4。相反,PDF响应根据受影响的离子通道进行分类。 PDF的应用有时会在同一神经元中抑制向外的钾或向内的钠电流。在对Ca 2 + 成像和膜片钳实验的比较中,我们假设在1型细胞中,依赖cAMP的PDF依赖性升高主要阻断了向外的K + 电流。可能,这种依赖于PDF的去极化是起搏器依赖于PDF的阶段发展的基础。最后,我们提出耦合起搏器中K + 和Na + 通道的PDF依赖性伴随调制会引起超膜电位振荡,这是通过共振有效同步的前提。

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