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A hypothalamic novelty signal modulates hippocampal memory

Author

Listed:
  • Shuo Chen

    (RIKEN Center for Brain Science)

  • Linmeng He

    (RIKEN Center for Brain Science
    The University of Tokyo)

  • Arthur J. Y. Huang

    (RIKEN Center for Brain Science)

  • Roman Boehringer

    (RIKEN Center for Brain Science)

  • Vincent Robert

    (Université de Paris, INSERM UMRS1266)

  • Marie E. Wintzer

    (RIKEN Center for Brain Science)

  • Denis Polygalov

    (RIKEN Center for Brain Science)

  • Adam Z. Weitemier

    (RIKEN Center for Brain Science)

  • Yanqiu Tao

    (RIKEN Center for Brain Science)

  • Mingxiao Gu

    (RIKEN Center for Brain Science)

  • Steven J. Middleton

    (RIKEN Center for Brain Science)

  • Kana Namiki

    (RIKEN Center for Brain Science)

  • Hiroshi Hama

    (RIKEN Center for Brain Science)

  • Ludivine Therreau

    (Université de Paris, INSERM UMRS1266)

  • Vivien Chevaleyre

    (Université de Paris, INSERM UMRS1266
    GHU PARIS Psychiatry and Neuroscience)

  • Hiroyuki Hioki

    (Juntendo University Graduate School of Medicine)

  • Atsushi Miyawaki

    (RIKEN Center for Brain Science
    RIKEN Center for Advanced Photonics)

  • Rebecca A. Piskorowski

    (Université de Paris, INSERM UMRS1266
    GHU PARIS Psychiatry and Neuroscience)

  • Thomas J. McHugh

    (RIKEN Center for Brain Science
    The University of Tokyo)

Abstract

The ability to recognize information that is incongruous with previous experience is critical for survival. Novelty signals have therefore evolved in the mammalian brain to enhance attention, perception and memory1,2. Although the importance of regions such as the ventral tegmental area3,4 and locus coeruleus5 in broadly signalling novelty is well-established, these diffuse monoaminergic transmitters have yet to be shown to convey specific information on the type of stimuli that drive them. Whether distinct types of novelty, such as contextual and social novelty, are differently processed and routed in the brain is unknown. Here we identify the supramammillary nucleus (SuM) as a novelty hub in the hypothalamus6. The SuM region is unique in that it not only responds broadly to novel stimuli, but also segregates and selectively routes different types of information to discrete cortical targets—the dentate gyrus and CA2 fields of the hippocampus—for the modulation of mnemonic processing. Using a new transgenic mouse line, SuM-Cre, we found that SuM neurons that project to the dentate gyrus are activated by contextual novelty, whereas the SuM–CA2 circuit is preferentially activated by novel social encounters. Circuit-based manipulation showed that divergent novelty channelling in these projections modifies hippocampal contextual or social memory. This content-specific routing of novelty signals represents a previously unknown mechanism that enables the hypothalamus to flexibly modulate select components of cognition.

Suggested Citation

  • Shuo Chen & Linmeng He & Arthur J. Y. Huang & Roman Boehringer & Vincent Robert & Marie E. Wintzer & Denis Polygalov & Adam Z. Weitemier & Yanqiu Tao & Mingxiao Gu & Steven J. Middleton & Kana Namiki , 2020. "A hypothalamic novelty signal modulates hippocampal memory," Nature, Nature, vol. 586(7828), pages 270-274, October.
  • Handle: RePEc:nat:nature:v:586:y:2020:i:7828:d:10.1038_s41586-020-2771-1
    DOI: 10.1038/s41586-020-2771-1
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    Citations

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    Cited by:

    1. Stefano Garofalo & Germana Cocozza & Alessandro Mormino & Giovanni Bernardini & Eleonora Russo & Donald Ielpo & Diego Andolina & Rossella Ventura & Katiuscia Martinello & Massimiliano Renzi & Sergio F, 2023. "Natural killer cells and innate lymphoid cells 1 tune anxiety-like behavior and memory in mice via interferon-γ and acetylcholine," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    2. Elise C. Cope & Samantha H. Wang & Renée C. Waters & Isha R. Gore & Betsy Vasquez & Blake J. Laham & Elizabeth Gould, 2023. "Activation of the CA2-ventral CA1 pathway reverses social discrimination dysfunction in Shank3B knockout mice," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    3. Susanna Molas & Timothy G. Freels & Rubing Zhao-Shea & Timothy Lee & Pablo Gimenez-Gomez & Melanie Barbini & Gilles E. Martin & Andrew R. Tapper, 2024. "Dopamine control of social novelty preference is constrained by an interpeduncular-tegmentum circuit," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    4. Ruy Gómez-Ocádiz & Massimiliano Trippa & Chun-Lei Zhang & Lorenzo Posani & Simona Cocco & Rémi Monasson & Christoph Schmidt-Hieber, 2022. "A synaptic signal for novelty processing in the hippocampus," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    5. Qingtao Sun & Jianping Zhang & Anan Li & Mei Yao & Guangcai Liu & Siqi Chen & Yue Luo & Zhi Wang & Hui Gong & Xiangning Li & Qingming Luo, 2022. "Acetylcholine deficiency disrupts extratelencephalic projection neurons in the prefrontal cortex in a mouse model of Alzheimer’s disease," Nature Communications, Nature, vol. 13(1), pages 1-22, December.

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