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Suprachiasmatic VIP neurons are required for normal circadian rhythmicity and comprised of molecularly distinct subpopulations

Author

Listed:
  • William D. Todd

    (University of Wyoming)

  • Anne Venner

    (Division of Sleep Medicine, Harvard Medical School)

  • Christelle Anaclet

    (University of Massachusetts Medical School)

  • Rebecca Y. Broadhurst

    (Division of Sleep Medicine, Harvard Medical School)

  • Roberto Luca

    (Division of Sleep Medicine, Harvard Medical School)

  • Sathyajit S. Bandaru

    (Division of Sleep Medicine, Harvard Medical School)

  • Lindsay Issokson

    (Division of Sleep Medicine, Harvard Medical School)

  • Lauren M. Hablitz

    (Oregon Health & Science University)

  • Olga Cravetchi

    (Oregon Health & Science University)

  • Elda Arrigoni

    (Division of Sleep Medicine, Harvard Medical School)

  • John N. Campbell

    (University of Virginia)

  • Charles N. Allen

    (Oregon Health & Science University)

  • David P. Olson

    (University of Michigan)

  • Patrick M. Fuller

    (Division of Sleep Medicine, Harvard Medical School)

Abstract

The hypothalamic suprachiasmatic (SCN) clock contains several neurochemically defined cell groups that contribute to the genesis of circadian rhythms. Using cell-specific and genetically targeted approaches we have confirmed an indispensable role for vasoactive intestinal polypeptide-expressing SCN (SCNVIP) neurons, including their molecular clock, in generating the mammalian locomotor activity (LMA) circadian rhythm. Optogenetic-assisted circuit mapping revealed functional, di-synaptic connectivity between SCNVIP neurons and dorsomedial hypothalamic neurons, providing a circuit substrate by which SCNVIP neurons may regulate LMA rhythms. In vivo photometry revealed that while SCNVIP neurons are acutely responsive to light, their activity is otherwise behavioral state invariant. Single-nuclei RNA-sequencing revealed that SCNVIP neurons comprise two transcriptionally distinct subtypes, including putative pacemaker and non-pacemaker populations. Altogether, our work establishes necessity of SCNVIP neurons for the LMA circadian rhythm, elucidates organization of circadian outflow from and modulatory input to SCNVIP cells, and demonstrates a subpopulation-level molecular heterogeneity that suggests distinct functions for specific SCNVIP subtypes.

Suggested Citation

  • William D. Todd & Anne Venner & Christelle Anaclet & Rebecca Y. Broadhurst & Roberto Luca & Sathyajit S. Bandaru & Lindsay Issokson & Lauren M. Hablitz & Olga Cravetchi & Elda Arrigoni & John N. Campb, 2020. "Suprachiasmatic VIP neurons are required for normal circadian rhythmicity and comprised of molecularly distinct subpopulations," Nature Communications, Nature, vol. 11(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17197-2
    DOI: 10.1038/s41467-020-17197-2
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    Cited by:

    1. Andrew E. Warfield & Pooja Gupta & Madison M. Ruhmann & Quiana L. Jeffs & Genevieve C. Guidone & Hannah W. Rhymes & McKenzi I. Thompson & William D. Todd, 2023. "A brainstem to circadian system circuit links Tau pathology to sundowning-related disturbances in an Alzheimer’s disease mouse model," Nature Communications, Nature, vol. 14(1), pages 1-17, December.

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