Rhythmic cilia changes support SCN neuron coherence in circadian clock

The suprachiasmatic nucleus (SCN) drives circadian clock coherence through intercellular coupling, which is resistant to environmental perturbations. We report that primary cilia are required for intercellular coupling among SCN neurons to maintain the robustness of the internal clock in mice. Cilia...

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Published inScience (American Association for the Advancement of Science) Vol. 380; no. 6648; pp. 972 - 979
Main Authors Tu, Hai-Qing, Li, Sen, Xu, Yu-Ling, Zhang, Yu-Cheng, Li, Pei-Yao, Liang, Li-Yun, Song, Guang-Ping, Jian, Xiao-Xiao, Wu, Min, Song, Zeng-Qing, Li, Ting-Ting, Hu, Huai-Bin, Yuan, Jin-Feng, Shen, Xiao-Lin, Li, Jia-Ning, Han, Qiu-Ying, Wang, Kai, Zhang, Tao, Zhou, Tao, Li, Ai-Ling, Zhang, Xue-Min, Li, Hui-Yan
Format Journal Article
LanguageEnglish
Published United States The American Association for the Advancement of Science 02.06.2023
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Abstract The suprachiasmatic nucleus (SCN) drives circadian clock coherence through intercellular coupling, which is resistant to environmental perturbations. We report that primary cilia are required for intercellular coupling among SCN neurons to maintain the robustness of the internal clock in mice. Cilia in neuromedin S–producing (NMS) neurons exhibit pronounced circadian rhythmicity in abundance and length. Genetic ablation of ciliogenesis in NMS neurons enabled a rapid phase shift of the internal clock under jet-lag conditions. The circadian rhythms of individual neurons in cilia-deficient SCN slices lost their coherence after external perturbations. Rhythmic cilia changes drive oscillations of Sonic Hedgehog (Shh) signaling and clock gene expression. Inactivation of Shh signaling in NMS neurons phenocopied the effects of cilia ablation. Thus, cilia-Shh signaling in the SCN aids intercellular coupling. Coordination of physiology with daily rhythms is regulated by the neurons of the suprachiasmatic nucleus (SCN), the central pacemaker of the biological clock. Tu et al . describe a signaling mechanism at cilia in these neurons that keeps the individual cells of the SCN synchronized (see the Perspective by Kim and Blackshaw). The length and abundance of primary cilia in SCN neurons oscillated with daily light-dark cycles. Cilia organize signaling by the morphogen Sonic Hedgehog (SHH), and regulation of the expression of this gene was required for synchrony of the SCN cells. In mice exposed to an altered light cycle to induce experimental jet lag, disrupting SHH signaling allowed the animals to adjust more quickly to the altered environment. —L. Bryan Ray Signaling at cilia helps couple neurons in the master biological clock in the brain.
AbstractList Editor’s summaryCoordination of physiology with daily rhythms is regulated by the neurons of the suprachiasmatic nucleus (SCN), the central pacemaker of the biological clock. Tu et al. describe a signaling mechanism at cilia in these neurons that keeps the individual cells of the SCN synchronized (see the Perspective by Kim and Blackshaw). The length and abundance of primary cilia in SCN neurons oscillated with daily light-dark cycles. Cilia organize signaling by the morphogen Sonic Hedgehog (SHH), and regulation of the expression of this gene was required for synchrony of the SCN cells. In mice exposed to an altered light cycle to induce experimental jet lag, disrupting SHH signaling allowed the animals to adjust more quickly to the altered environment. —L. Bryan Ray
The suprachiasmatic nucleus (SCN) drives circadian clock coherence through intercellular coupling, which is resistant to environmental perturbations. We report that primary cilia are required for intercellular coupling among SCN neurons to maintain the robustness of the internal clock in mice. Cilia in neuromedin S-producing (NMS) neurons exhibit pronounced circadian rhythmicity in abundance and length. Genetic ablation of ciliogenesis in NMS neurons enabled a rapid phase shift of the internal clock under jet-lag conditions. The circadian rhythms of individual neurons in cilia-deficient SCN slices lost their coherence after external perturbations. Rhythmic cilia changes drive oscillations of Sonic Hedgehog (Shh) signaling and clock gene expression. Inactivation of Shh signaling in NMS neurons phenocopied the effects of cilia ablation. Thus, cilia-Shh signaling in the SCN aids intercellular coupling.
The suprachiasmatic nucleus (SCN) drives circadian clock coherence through intercellular coupling, which is resistant to environmental perturbations. We report that primary cilia are required for intercellular coupling among SCN neurons to maintain the robustness of the internal clock in mice. Cilia in neuromedin S-producing (NMS) neurons exhibit pronounced circadian rhythmicity in abundance and length. Genetic ablation of ciliogenesis in NMS neurons enabled a rapid phase shift of the internal clock under jet-lag conditions. The circadian rhythms of individual neurons in cilia-deficient SCN slices lost their coherence after external perturbations. Rhythmic cilia changes drive oscillations of Sonic Hedgehog (Shh) signaling and clock gene expression. Inactivation of Shh signaling in NMS neurons phenocopied the effects of cilia ablation. Thus, cilia-Shh signaling in the SCN aids intercellular coupling.The suprachiasmatic nucleus (SCN) drives circadian clock coherence through intercellular coupling, which is resistant to environmental perturbations. We report that primary cilia are required for intercellular coupling among SCN neurons to maintain the robustness of the internal clock in mice. Cilia in neuromedin S-producing (NMS) neurons exhibit pronounced circadian rhythmicity in abundance and length. Genetic ablation of ciliogenesis in NMS neurons enabled a rapid phase shift of the internal clock under jet-lag conditions. The circadian rhythms of individual neurons in cilia-deficient SCN slices lost their coherence after external perturbations. Rhythmic cilia changes drive oscillations of Sonic Hedgehog (Shh) signaling and clock gene expression. Inactivation of Shh signaling in NMS neurons phenocopied the effects of cilia ablation. Thus, cilia-Shh signaling in the SCN aids intercellular coupling.
The suprachiasmatic nucleus (SCN) drives circadian clock coherence through intercellular coupling, which is resistant to environmental perturbations. We report that primary cilia are required for intercellular coupling among SCN neurons to maintain the robustness of the internal clock in mice. Cilia in neuromedin S–producing (NMS) neurons exhibit pronounced circadian rhythmicity in abundance and length. Genetic ablation of ciliogenesis in NMS neurons enabled a rapid phase shift of the internal clock under jet-lag conditions. The circadian rhythms of individual neurons in cilia-deficient SCN slices lost their coherence after external perturbations. Rhythmic cilia changes drive oscillations of Sonic Hedgehog (Shh) signaling and clock gene expression. Inactivation of Shh signaling in NMS neurons phenocopied the effects of cilia ablation. Thus, cilia-Shh signaling in the SCN aids intercellular coupling. Coordination of physiology with daily rhythms is regulated by the neurons of the suprachiasmatic nucleus (SCN), the central pacemaker of the biological clock. Tu et al . describe a signaling mechanism at cilia in these neurons that keeps the individual cells of the SCN synchronized (see the Perspective by Kim and Blackshaw). The length and abundance of primary cilia in SCN neurons oscillated with daily light-dark cycles. Cilia organize signaling by the morphogen Sonic Hedgehog (SHH), and regulation of the expression of this gene was required for synchrony of the SCN cells. In mice exposed to an altered light cycle to induce experimental jet lag, disrupting SHH signaling allowed the animals to adjust more quickly to the altered environment. —L. Bryan Ray Signaling at cilia helps couple neurons in the master biological clock in the brain.
Author Wu, Min
Zhang, Xue-Min
Song, Guang-Ping
Zhou, Tao
Yuan, Jin-Feng
Li, Ai-Ling
Li, Sen
Jian, Xiao-Xiao
Hu, Huai-Bin
Li, Pei-Yao
Shen, Xiao-Lin
Xu, Yu-Ling
Li, Jia-Ning
Song, Zeng-Qing
Han, Qiu-Ying
Li, Hui-Yan
Tu, Hai-Qing
Liang, Li-Yun
Wang, Kai
Zhang, Yu-Cheng
Li, Ting-Ting
Zhang, Tao
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Snippet The suprachiasmatic nucleus (SCN) drives circadian clock coherence through intercellular coupling, which is resistant to environmental perturbations. We report...
Editor’s summaryCoordination of physiology with daily rhythms is regulated by the neurons of the suprachiasmatic nucleus (SCN), the central pacemaker of the...
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SubjectTerms Animals
Biological clocks
Cilia
Cilia - metabolism
Cilia - physiology
Circadian Clocks - genetics
Circadian Rhythm - physiology
Circadian rhythms
Gene expression
Gene Expression Regulation
Hedgehog protein
Hedgehog Proteins - genetics
Hedgehog Proteins - metabolism
Jet lag
Mice
Mice, Transgenic
Neurons
Signal Transduction
Signaling
Suprachiasmatic nucleus
Suprachiasmatic Nucleus Neurons - physiology
Title Rhythmic cilia changes support SCN neuron coherence in circadian clock
URI https://www.ncbi.nlm.nih.gov/pubmed/37262147
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https://www.proquest.com/docview/2822371892
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