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睡眠活跃神经元可在睡眠行为受到干扰时促进生存。

A sleep-active neuron can promote survival while sleep behavior is disturbed.

机构信息

BIOTEC, Technical University Dresden, Dresden, Germany.

出版信息

PLoS Genet. 2023 Mar 14;19(3):e1010665. doi: 10.1371/journal.pgen.1010665. eCollection 2023 Mar.

Abstract

Sleep is controlled by neurons that induce behavioral quiescence and physiological restoration. It is not known, however, how sleep neurons link sleep behavior and survival. In Caenorhabditis elegans, the sleep-active RIS neuron induces sleep behavior and is required for survival of starvation and wounding. Sleep-active neurons such as RIS might hypothetically promote survival primarily by causing sleep behavior and associated conservation of energy. Alternatively, RIS might provide a survival benefit that does not depend on behavioral sleep. To probe these hypotheses, we tested how activity of the sleep-active RIS neuron in Caenorhabditis elegans controls sleep behavior and survival during larval starvation. To manipulate the activity of RIS, we expressed constitutively active potassium channel (twk-18gf and egl-23gf) or sodium channel (unc-58gf) mutant alleles in this neuron. Low levels of unc-58gf expression in RIS increased RIS calcium transients and sleep. High levels of unc-58gf expression in RIS elevated baseline calcium activity and inhibited calcium activation transients, thus locking RIS activity at a high but constant level. This manipulation caused a nearly complete loss of sleep behavior but increased survival. Long-term optogenetic activation also caused constantly elevated RIS activity and a small trend towards increased survival. Disturbing sleep by lethal blue-light stimulation also overactivated RIS, which again increased survival. FLP-11 neuropeptides were important for both, induction of sleep behavior and starvation survival, suggesting that FLP-11 might have divergent roles downstream of RIS. These results indicate that promotion of sleep behavior and survival are separable functions of RIS. These two functions may normally be coupled but can be uncoupled during conditions of strong RIS activation or when sleep behavior is impaired. Through this uncoupling, RIS can provide survival benefits under conditions when behavioral sleep is disturbed. Promoting survival in the face of impaired sleep might be a general function of sleep neurons.

摘要

睡眠受诱导行为静止和生理恢复的神经元控制。然而,尚不清楚睡眠神经元如何将睡眠行为与生存联系起来。在秀丽隐杆线虫中,睡眠活跃的 RIS 神经元诱导睡眠行为,并且是饥饿和受伤时生存所必需的。像 RIS 这样的睡眠活跃神经元可能从理论上主要通过引起睡眠行为和相关的能量保存来促进生存。或者,RIS 可能提供一种不依赖于行为性睡眠的生存益处。为了探究这些假设,我们测试了秀丽隐杆线虫中活跃的睡眠神经元 RIS 的活动如何控制幼虫饥饿期间的睡眠行为和生存。为了操纵 RIS 的活动,我们在这个神经元中表达组成型活性钾通道(twk-18gf 和 egl-23gf)或钠通道(unc-58gf)突变等位基因。RIS 中低水平的 unc-58gf 表达增加了 RIS 的钙瞬变和睡眠。RIS 中高水平的 unc-58gf 表达提高了基线钙活性并抑制了钙激活瞬变,从而将 RIS 活性锁定在一个高但恒定的水平。这种操作导致几乎完全丧失睡眠行为,但增加了生存。长期光遗传学激活也导致 RIS 活性持续升高,并略有增加生存的趋势。通过致死性蓝光刺激扰乱睡眠也过度激活了 RIS,这再次增加了生存。FLP-11 神经肽对于诱导睡眠行为和饥饿生存都很重要,这表明 FLP-11 可能在 RIS 下游具有不同的作用。这些结果表明,促进睡眠行为和生存是 RIS 的分离功能。这两个功能通常是耦合的,但在 RIS 强烈激活或睡眠行为受损的情况下可以解耦。通过这种解耦,RIS 可以在行为性睡眠受到干扰的情况下提供生存益处。在睡眠受损的情况下促进生存可能是睡眠神经元的一般功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7765/10038310/df1e4260819c/pgen.1010665.g001.jpg

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