Title |
The cerebellum promotes sequential foraging strategies and contributes to the directional modulation of hippocampal place cells |
Authors |
Zhang,Lu;Neuroscience Paris-Seine – Institut de biologie Paris-Seine, Sorbonne Université, INSERM, CNRS, Paris, France
Fournier,Julien;Neuroscience Paris-Seine – Institut de biologie Paris-Seine, Sorbonne Université, INSERM, CNRS, Paris, France;ORCID: 0000-0001-7167-8132
Fallahnezhad,Mehdi;Neuroscience Paris-Seine – Institut de biologie Paris-Seine, Sorbonne Université, INSERM, CNRS, Paris, France;ORCID: 0000-0002-7968-1771
Paradis,Anne-Lise;Neuroscience Paris-Seine – Institut de biologie Paris-Seine, Sorbonne Université, INSERM, CNRS, Paris, France;ORCID: 0000-0002-5933-0448
Rochefort,Christelle;Neuroscience Paris-Seine – Institut de biologie Paris-Seine, Sorbonne Université, INSERM, CNRS, Paris, France;ORCID: 0000-0001-8466-5218
Rondi-Reig,Laure;Neuroscience Paris-Seine – Institut de biologie Paris-Seine, Sorbonne Université, INSERM, CNRS, Paris, France;ORCID: 0000-0003-1006-0501
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Description |
The cerebellum contributes to spatial coding in the hippocampus.
When PKC-dependent mechanisms are impaired in cerebellar Purkinje cells,
hippocampal place cells indeed lose their spatial selectivity in the dark,
when the animal relies mostly on self-motion cues to navigate.
This impairment in PKC-dependent cerebellar functions additionally
leads to behavioral deficits in using both external and self-motion
cues when learning a goal-oriented navigation task. However, it is
unclear how cerebellum influences the exploration strategy used by
an animal during free foraging in an open environment.
Here we recorded hippocampal place cells in mice with impaired PKC-dependent
mechanisms (L7-PKCI) and in their littermate controls while they performed a
foraging task where they were rewarded for visiting a subset of
hidden locations. We found that L7-PKCI and control mice developed different
foraging strategies: while control mice repeated reliable spatial sequences
to maximize their rewards, L7-PKCI mice persisted to use a random foraging
strategy. The sequence-based strategy was associated with more place cells
exhibiting theta-phase precession and theta modulation. It was also correlated
with a larger fraction of place cells that were modulated concomitantly by
movement direction and speed. Finally, in the dark, the modulation of place
cells by movement direction was markedly reduced in L7-PKCI mice, demonstrating
that PKC-dependent cerebellar functions control how self-motion cues influence
not only position but also direction coding in the hippocampus. Thus, the cerebellum
contributes to the development of optimal sequential paths during foraging,
possibly by controlling how self-motion and theta signals contribute to place cells coding.
This data set includes behavioral tracking data corresponding to several
navigational variables such as position, movement direction, speed and
reward delivery. For sessions where behavior was combined with hippocampal
recordings, it also includes spike times from hippocampal single units and
LFP oscillations.
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License |
Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/)
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References |
Lu Zhang*, Julien Fournier*, Mehdi Fallahnezhad, Anne-Lise Paradis, Christelle Rochefort, Laure Rondi-Reig (2023). The cerebellum promotes sequential foraging strategies and contributes to the directional modulation of hippocampal place cells, iScience. [doi:tba] (IsSupplementTo)
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Funding |
Fondation pour la Recherche Médicale, DEQ20160334907-France
National Agency for Research, ANR-17-CE37-0015-01 and ANR-18-CE16-0010-02
Human Frontier Science program CDA 00058 -2019
Institut Universitaire de France
CNRS
INSERM
Sorbonne Universites
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Keywords |
Neuroscience
Navigation
Cerebellum
Hippocampus
Place cells
Theta phase precession
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Resource Type |
Dataset
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