The rapid developmental rise of somatic inhibition disengages hippocampal dynamics from self-motion

  1. Robin F Dard
  2. Erwan Leprince
  3. Julien Denis
  4. Shrisha Rao Balappa
  5. Dmitrii Suchkov
  6. Richard Boyce
  7. Catherine Lopez
  8. Marie Giorgi-Kurz
  9. Tom Szwagier
  10. Théo Dumont
  11. Hervé Rouault
  12. Marat Minlebaev
  13. Agnès Baude
  14. Rosa Cossart  Is a corresponding author
  15. Michel A Picardo  Is a corresponding author
  1. Aix Marseille Univ, INSERM, INMED U1249, France
  2. Aix-Marseille Univ, Université de Toulon, CNRS, CPT (UMR 7332), France
  3. Mines ParisTech, France

Abstract

Early electrophysiological brain oscillations recorded in preterm babies and newborn rodents are initially mostly driven by bottom-up sensorimotor activity and only later can detach from external inputs. This is a hallmark of most developing brain areas including the hippocampus, which in the adult brain, functions in integrating external inputs onto internal dynamics. Such developmental disengagement from external inputs is likely a fundamental step for the proper development of cognitive internal models. Despite its importance, the developmental timeline and circuit basis for this disengagement remain unknown. To address this issue, we have investigated the daily evolution of CA1 dynamics and underlying circuits during the first two postnatal weeks of mouse development using two-photon calcium imaging in non-anesthetized pups. We show that the first postnatal week ends with an abrupt shift in the representation of self-motion in CA1. Indeed, most CA1 pyramidal cells switch from activated to inhibited by self-generated movements at the end of the first postnatal week whereas the majority of GABAergic neurons remain positively modulated throughout this period. This rapid switch occurs within two days and follows the rapid anatomical and functional surge of local somatic GABAergic innervation. The observed change in dynamics is consistent with a two-population model undergoing a strengthening of inhibition. We propose that this abrupt developmental transition inaugurates the emergence of internal hippocampal dynamics.

Data availability

NWB dataset is available at DANDI Archive (https://dandiarchive.org 000219).All codes are on GITLAB (Cossart Lab - GitLab).

The following data sets were generated

Article and author information

Author details

  1. Robin F Dard

    Turing Centre for Living systems, Aix Marseille Univ, INSERM, INMED U1249, Marseille, France
    Competing interests
    The authors declare that no competing interests exist.
  2. Erwan Leprince

    Turing Centre for Living systems, Aix Marseille Univ, INSERM, INMED U1249, Marseille, France
    Competing interests
    The authors declare that no competing interests exist.
  3. Julien Denis

    Turing Centre for Living systems, Aix Marseille Univ, INSERM, INMED U1249, Marseille, France
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-0537-6483
  4. Shrisha Rao Balappa

    Turing Centre for Living systems, Aix-Marseille Univ, Université de Toulon, CNRS, CPT (UMR 7332), Marseille, France
    Competing interests
    The authors declare that no competing interests exist.
  5. Dmitrii Suchkov

    Turing Centre for Living systems, Aix Marseille Univ, INSERM, INMED U1249, Marseille, France
    Competing interests
    The authors declare that no competing interests exist.
  6. Richard Boyce

    Turing Centre for Living systems, Aix Marseille Univ, INSERM, INMED U1249, Marseille, France
    Competing interests
    The authors declare that no competing interests exist.
  7. Catherine Lopez

    Turing Centre for Living systems, Aix Marseille Univ, INSERM, INMED U1249, Marseille, France
    Competing interests
    The authors declare that no competing interests exist.
  8. Marie Giorgi-Kurz

    Turing Centre for Living systems, Aix Marseille Univ, INSERM, INMED U1249, Marseille, France
    Competing interests
    The authors declare that no competing interests exist.
  9. Tom Szwagier

    Mines ParisTech, Paris, France
    Competing interests
    The authors declare that no competing interests exist.
  10. Théo Dumont

    Mines ParisTech, Paris, France
    Competing interests
    The authors declare that no competing interests exist.
  11. Hervé Rouault

    Turing Centre for Living systems, Aix-Marseille Univ, Université de Toulon, CNRS, CPT (UMR 7332), Marseille, France
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-4997-2711
  12. Marat Minlebaev

    Turing Centre for Living systems, Aix Marseille Univ, INSERM, INMED U1249, Marseille, France
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-0722-7027
  13. Agnès Baude

    Turing Centre for Living systems, Aix Marseille Univ, INSERM, INMED U1249, Marseille, France
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-7025-364X
  14. Rosa Cossart

    Turing Centre for Living systems, Aix Marseille Univ, INSERM, INMED U1249, Marseille, France
    For correspondence
    rosa.cossart@inserm.fr
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-2111-6638
  15. Michel A Picardo

    Turing Centre for Living systems, Aix Marseille Univ, INSERM, INMED U1249, Marseille, France
    For correspondence
    michel.picardo@inserm.fr
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-1198-3930

Funding

European Resuscitation Council (646925)

  • Rosa Cossart

Fondation Bettencourt Schueller

  • Rosa Cossart

Neurodata Without Borders (R20046AA)

  • Michel A Picardo

Agence Nationale de la Recherche (ANR-16-CONV-0001)

  • Rosa Cossart

Ministère de l'Education Nationale, de l'Enseignement Superieur et de la Recherche (MESR)

  • Robin F Dard
  • Erwan Leprince

Fondation pour la Recherche Médicale (FDT202106012824)

  • Robin F Dard

Fondation pour la Recherche Médicale (FDM20170638339)

  • Julien Denis

Fondation pour la Recherche Médicale (ARF20160936186)

  • Michel A Picardo

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Ethics

Animal experimentation: All experiments were performed under the guidelines of the French National Ethics Committee forSciences and Health report on "Ethical Principles for Animal Experimentation" in agreement with theEuropean Community Directive 86/609/EEC (Apafis#18-185 and #30-959).

Copyright

© 2022, Dard et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 2,227
    views
  • 363
    downloads
  • 28
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Robin F Dard
  2. Erwan Leprince
  3. Julien Denis
  4. Shrisha Rao Balappa
  5. Dmitrii Suchkov
  6. Richard Boyce
  7. Catherine Lopez
  8. Marie Giorgi-Kurz
  9. Tom Szwagier
  10. Théo Dumont
  11. Hervé Rouault
  12. Marat Minlebaev
  13. Agnès Baude
  14. Rosa Cossart
  15. Michel A Picardo
(2022)
The rapid developmental rise of somatic inhibition disengages hippocampal dynamics from self-motion
eLife 11:e78116.
https://doi.org/10.7554/eLife.78116

Share this article

https://doi.org/10.7554/eLife.78116

Further reading

    1. Neuroscience
    Gergely F Turi, Sasa Teng ... Yueqing Peng
    Research Article

    Synchronous neuronal activity is organized into neuronal oscillations with various frequency and time domains across different brain areas and brain states. For example, hippocampal theta, gamma, and sharp wave oscillations are critical for memory formation and communication between hippocampal subareas and the cortex. In this study, we investigated the neuronal activity of the dentate gyrus (DG) with optical imaging tools during sleep-wake cycles in mice. We found that the activity of major glutamatergic cell populations in the DG is organized into infraslow oscillations (0.01–0.03 Hz) during NREM sleep. Although the DG is considered a sparsely active network during wakefulness, we found that 50% of granule cells and about 25% of mossy cells exhibit increased activity during NREM sleep, compared to that during wakefulness. Further experiments revealed that the infraslow oscillation in the DG was correlated with rhythmic serotonin release during sleep, which oscillates at the same frequency but in an opposite phase. Genetic manipulation of 5-HT receptors revealed that this neuromodulatory regulation is mediated by Htr1a receptors and the knockdown of these receptors leads to memory impairment. Together, our results provide novel mechanistic insights into how the 5-HT system can influence hippocampal activity patterns during sleep.

    1. Neuroscience
    Ulrike Pech, Jasper Janssens ... Patrik Verstreken
    Research Article

    The classical diagnosis of Parkinsonism is based on motor symptoms that are the consequence of nigrostriatal pathway dysfunction and reduced dopaminergic output. However, a decade prior to the emergence of motor issues, patients frequently experience non-motor symptoms, such as a reduced sense of smell (hyposmia). The cellular and molecular bases for these early defects remain enigmatic. To explore this, we developed a new collection of five fruit fly models of familial Parkinsonism and conducted single-cell RNA sequencing on young brains of these models. Interestingly, cholinergic projection neurons are the most vulnerable cells, and genes associated with presynaptic function are the most deregulated. Additional single nucleus sequencing of three specific brain regions of Parkinson’s disease patients confirms these findings. Indeed, the disturbances lead to early synaptic dysfunction, notably affecting cholinergic olfactory projection neurons crucial for olfactory function in flies. Correcting these defects specifically in olfactory cholinergic interneurons in flies or inducing cholinergic signaling in Parkinson mutant human induced dopaminergic neurons in vitro using nicotine, both rescue age-dependent dopaminergic neuron decline. Hence, our research uncovers that one of the earliest indicators of disease in five different models of familial Parkinsonism is synaptic dysfunction in higher-order cholinergic projection neurons and this contributes to the development of hyposmia. Furthermore, the shared pathways of synaptic failure in these cholinergic neurons ultimately contribute to dopaminergic dysfunction later in life.