Literature DB >> 33510164

Mouse entorhinal cortex encodes a diverse repertoire of self-motion signals.

Caitlin S Mallory1, Kiah Hardcastle1, Malcolm G Campbell1, Alexander Attinger1, Isabel I C Low1, Jennifer L Raymond1, Lisa M Giocomo2.   

Abstract

Neural circuits generate representations of the external world from multiple information streams. The navigation system provides an exceptional lens through which we may gain insights about how such computations are implemented. Neural circuits in the medial temporal lobe construct a map-like representation of space that supports navigation. This computation integrates multiple sensory cues, and, in addition, is thought to require cues related to the individual's movement through the environment. Here, we identify multiple self-motion signals, related to the position and velocity of the head and eyes, encoded by neurons in a key node of the navigation circuitry of mice, the medial entorhinal cortex (MEC). The representation of these signals is highly integrated with other cues in individual neurons. Such information could be used to compute the allocentric location of landmarks from visual cues and to generate internal representations of space.

Entities:  

Year:  2021        PMID: 33510164      PMCID: PMC7844029          DOI: 10.1038/s41467-021-20936-8

Source DB:  PubMed          Journal:  Nat Commun        ISSN: 2041-1723            Impact factor:   14.919


  56 in total

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Review 3.  Path integration and the neural basis of the 'cognitive map'.

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Journal:  Nat Rev Neurosci       Date:  2006-08       Impact factor: 34.870

4.  Genome-wide atlas of gene expression in the adult mouse brain.

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Authors:  Elisha P Merriam; Justin L Gardner; J Anthony Movshon; David J Heeger
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6.  Visual landmarks facilitate rodent spatial navigation in virtual reality environments.

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Journal:  Learn Mem       Date:  2012-02-15       Impact factor: 2.460

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Authors:  R W Stackman; J S Taube
Journal:  J Neurosci       Date:  1998-11-01       Impact factor: 6.167

8.  Streamlined sensory motor communication through cortical reciprocal connectivity in a visually guided eye movement task.

Authors:  Takahide Itokazu; Masashi Hasegawa; Rui Kimura; Hironobu Osaki; Urban-Raphael Albrecht; Kazuhiro Sohya; Shubhodeep Chakrabarti; Hideaki Itoh; Tetsufumi Ito; Tatsuo K Sato; Takashi R Sato
Journal:  Nat Commun       Date:  2018-01-23       Impact factor: 14.919

9.  A unified approach to linking experimental, statistical and computational analysis of spike train data.

Authors:  Liang Meng; Mark A Kramer; Steven J Middleton; Miles A Whittington; Uri T Eden
Journal:  PLoS One       Date:  2014-01-17       Impact factor: 3.240

10.  Visual landmarks sharpen grid cell metric and confer context specificity to neurons of the medial entorhinal cortex.

Authors:  José Antonio Pérez-Escobar; Olga Kornienko; Patrick Latuske; Laura Kohler; Kevin Allen
Journal:  Elife       Date:  2016-07-23       Impact factor: 8.140

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  4 in total

1.  The Neurodata Without Borders ecosystem for neurophysiological data science.

Authors:  Oliver Rübel; Andrew Tritt; Ryan Ly; Benjamin K Dichter; Satrajit Ghosh; Lawrence Niu; Pamela Baker; Ivan Soltesz; Lydia Ng; Karel Svoboda; Loren Frank; Kristofer E Bouchard
Journal:  Elife       Date:  2022-10-04       Impact factor: 8.713

2.  Mapping vestibular and visual contributions to angular head velocity tuning in the cortex.

Authors:  Eivind Hennestad; Aree Witoelar; Anna R Chambers; Koen Vervaeke
Journal:  Cell Rep       Date:  2021-12-21       Impact factor: 9.423

3.  Multisensory coding of angular head velocity in the retrosplenial cortex.

Authors:  Sepiedeh Keshavarzi; Edward F Bracey; Richard A Faville; Dario Campagner; Adam L Tyson; Stephen C Lenzi; Tiago Branco; Troy W Margrie
Journal:  Neuron       Date:  2021-11-16       Impact factor: 17.173

4.  Angular and linear speed cells in the parahippocampal circuits.

Authors:  Davide Spalla; Alessandro Treves; Charlotte N Boccara
Journal:  Nat Commun       Date:  2022-04-07       Impact factor: 14.919

  4 in total

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