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A longitudinal study of Caenorhabditis elegans larvae reveals a novel locomotion switch regulated by Gαs signaling

机译:对秀丽隐杆线虫幼虫的纵向研究揭示了一种新的运动开关受Gαs信号调节

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摘要

Despite their simplicity, longitudinal studies of invertebrate models are rare. We thus sought to characterize behavioral trends of Caenorhabditis elegans, from the mid fourth larval stage through the mid young adult stage. We found that, outside of lethargus, animals exhibited abrupt switching between two distinct behavioral states: active wakefulness and quiet wakefulness. The durations of epochs of active wakefulness exhibited non-Poisson statistics. Increased Gαs signaling stabilized the active wakefulness state before, during and after lethargus. In contrast, decreased Gαs signaling, decreased neuropeptide release, or decreased CREB activity destabilized active wakefulness outside of, but not during, lethargus. Taken together, our findings support a model in which protein kinase A (PKA) stabilizes active wakefulness, at least in part through two of its downstream targets: neuropeptide release and CREB. However, during lethargus, when active wakefulness is strongly suppressed, the native role of PKA signaling in modulating locomotion and quiescence may be minor.>DOI:
机译:尽管简单,但无脊椎动物模型的纵向研究却很少。因此,我们试图表征秀丽隐杆线虫的行为趋势,从第四幼虫中期到年轻成年中期。我们发现,在食虫之外,动物表现出两种截然不同的行为状态之间的突然切换:主动觉醒和安静觉醒。主动觉醒的持续时间显示出非泊松统计。增加的Gαs信号可稳定嗜睡之前,之中和之后的活跃觉醒状态。相反,降低的Gαs信号传导,降低的神经肽释放或降低的CREB活性使嗜睡之外(但不是在此期间)使活跃的觉醒不稳定。综上所述,我们的发现支持一种模型,其中蛋白激酶A(PKA)至少部分通过其两个下游靶标(神经肽释放和CREB)稳定主动唤醒。但是,在嗜睡过程中,如果强烈抑制主动觉醒,则PKA信号在调节运动和静止中的固有作用可能很小。> DOI:

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