Suprachiasmatic nucleus VIPergic fibers show a circadian rhythm of expansion and retraction
In animals, overt circadian rhythms of physiology and behavior are centrally regulated by a circadian clock located in specific brain regions. In the fruit fly Drosophila and in mammals, these clocks rely on single-cell oscillators, but critical for their function as central circadian pacemakers are...
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Published in: | Current biology Vol. 34; no. 17; p. 4056 |
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09-09-2024
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Abstract | In animals, overt circadian rhythms of physiology and behavior are centrally regulated by a circadian clock located in specific brain regions. In the fruit fly Drosophila and in mammals, these clocks rely on single-cell oscillators, but critical for their function as central circadian pacemakers are network properties that change dynamically throughout the circadian cycle as well as in response to environmental stimuli.
In the fly, this plasticity involves circadian rhythms of expansion and retraction of clock neuron fibers.
Whether these drastic structural changes are a universal property of central neuronal pacemakers is unknown. To address this question, we studied neurons of the mouse suprachiasmatic nucleus (SCN) that express vasoactive intestinal polypeptide (VIP), which are critical for the SCN to function as a central circadian pacemaker. By targeting the expression of the fluorescent protein tdTomato to these neurons and using tissue clearing techniques to visualize all SCN VIPergic neurons and their fibers, we show that, similar to clock neurons in the fly, VIPergic fibers undergo a daily rhythm of expansion and retraction, with maximal branching during the day. This rhythm is circadian, as it persists under constant environmental conditions and is present in both males and females. We propose that circadian structural remodeling of clock neurons represents a key feature of central circadian pacemakers that is likely critical to regulate network properties, the response to environmental stimuli, and the regulation of circadian outputs. |
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AbstractList | In animals, overt circadian rhythms of physiology and behavior are centrally regulated by a circadian clock located in specific brain regions. In the fruit fly Drosophila and in mammals, these clocks rely on single-cell oscillators, but critical for their function as central circadian pacemakers are network properties that change dynamically throughout the circadian cycle as well as in response to environmental stimuli.
In the fly, this plasticity involves circadian rhythms of expansion and retraction of clock neuron fibers.
Whether these drastic structural changes are a universal property of central neuronal pacemakers is unknown. To address this question, we studied neurons of the mouse suprachiasmatic nucleus (SCN) that express vasoactive intestinal polypeptide (VIP), which are critical for the SCN to function as a central circadian pacemaker. By targeting the expression of the fluorescent protein tdTomato to these neurons and using tissue clearing techniques to visualize all SCN VIPergic neurons and their fibers, we show that, similar to clock neurons in the fly, VIPergic fibers undergo a daily rhythm of expansion and retraction, with maximal branching during the day. This rhythm is circadian, as it persists under constant environmental conditions and is present in both males and females. We propose that circadian structural remodeling of clock neurons represents a key feature of central circadian pacemakers that is likely critical to regulate network properties, the response to environmental stimuli, and the regulation of circadian outputs. |
Author | Ellisman, Mark H Carter, Bryn M de la Iglesia, Horacio O Ceriani, M Fernanda Neitz, Alexandra F |
Author_xml | – sequence: 1 givenname: Alexandra F surname: Neitz fullname: Neitz, Alexandra F organization: Department of Biology, University of Washington, Seattle, WA 98195-1800, USA; Molecular & Cellular Biology Graduate Program, University of Washington, Seattle, WA 98195, USA – sequence: 2 givenname: Bryn M surname: Carter fullname: Carter, Bryn M organization: Department of Biology, University of Washington, Seattle, WA 98195-1800, USA – sequence: 3 givenname: M Fernanda surname: Ceriani fullname: Ceriani, M Fernanda organization: Fundación Instituto Leloir, Buenos Aires C1405, Argentina – sequence: 4 givenname: Mark H surname: Ellisman fullname: Ellisman, Mark H organization: National Center for Molecular Imaging Research, Department of Neurosciences, School of Medicine, University of California, San Diego, La Jolla, CA 92093-0608, USA – sequence: 5 givenname: Horacio O surname: de la Iglesia fullname: de la Iglesia, Horacio O email: horaciod@uw.edu organization: Department of Biology, University of Washington, Seattle, WA 98195-1800, USA; Molecular & Cellular Biology Graduate Program, University of Washington, Seattle, WA 98195, USA. Electronic address: horaciod@uw.edu |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39127047$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Animals Circadian Rhythm - physiology Female Male Mice Mice, Inbred C57BL Neurons - metabolism Neurons - physiology Suprachiasmatic Nucleus - metabolism Suprachiasmatic Nucleus - physiology Vasoactive Intestinal Peptide - metabolism |
Title | Suprachiasmatic nucleus VIPergic fibers show a circadian rhythm of expansion and retraction |
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