Evidence map›Paper›PMID 29386117›Full record

ArticleCell reports2018

Stellate Cells in the Medial Entorhinal Cortex Are Required for Spatial Learning.

Sarah A Tennant, Lukas Fischer, Derek L F Garden, Klára Zsófia Gerlei, Cristina Martinez-Gonzalez, Christina McClure, Emma R Wood, Matthew F Nolan

Abstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

44 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Interneuron theta phase locking controls seizure susceptibility.bioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Article
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  14. Article
  15. Progressive Excitability Changes in the Medial Entorhinal Cortex in the 3xTg Mouse Model of Alzheimer's Disease Pathology.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  16. A consistent map in the medial entorhinal cortex supports spatial memory.bioRxiv : the preprint server for biology · 2023
    Article
  17. Review
  18. Article
  19. Article
  20. Reduced grid-like theta modulation in schizophrenia.Brain : a journal of neurology · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Sarah A TennantCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK.
Lukas FischerCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK.
Derek L F GardenCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK.
Klára Zsófia GerleiCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK.
Cristina Martinez-GonzalezCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK.
Christina McClureCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK.
Emma R WoodCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK.
Matthew F NolanCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK. Electronic address: mattnolan@ed.ac.uk.

Funding

Biotechnology and Biological Sciences Research Council BB/H020284/1Biotechnology and Biological Sciences Research Council BB/L010496/1Biotechnology and Biological Sciences Research Council BB/M010996/1Wellcome TrustWellcome Trust 200855/Z/16/ZWellcome Trust WT093295MA
6 · The paper itself

Abstract

Spatial learning requires estimates of location that may be obtained by path integration or from positional cues. Grid and other spatial firing patterns of neurons in the superficial medial entorhinal cortex (MEC) suggest roles in behavioral estimation of location. However, distinguishing the contributions of path integration and cue-based signals to spatial behaviors is challenging, and the roles of identified MEC neurons are unclear. We use virtual reality to dissociate linear path integration from other strategies for behavioral estimation of location. We find that mice learn to path integrate using motor-related self-motion signals, with accuracy that decreases steeply as a function of distance. We show that inactivation of stellate cells in superficial MEC impairs spatial learning in virtual reality and in a real world object location recognition task. Our results quantify contributions of path integration to behavior and corroborate key predictions of models in which stellate cells contribute to location estimation.

Indexed as

AnimalsEntorhinal CortexMiceNeuronsSpatial Learningbehaviorcue-based navigationentorhinal cortexlearninglocation estimationmemoryneural computationpath integrationspatial cognitionvirtual reality

Identifiers

PMID29386117
PMCPMC5809635

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.