Literature DB >> 29300838

Correlated Variability in the Neurons With the Strongest Tuning Improves Direction Coding.

Elizabeth Zavitz1,2,3, Hsin-Hao Yu1,2,3, Marcello G P Rosa1,2,3, Nicholas S C Price1,2,3.   

Abstract

Sensory perception depends on neuronal populations creating an accurate representation of the external world. The amount of information that a population can represent depends on the tuning of individual neurons and the trial-by-trial variability shared among neurons. Although on average, pairwise spike-count correlations between neurons are positive, the distribution is wide, and the relationship between correlations and encoding is not straightforward. Here, we examine how single-neuron and population-level factors impact the efficacy of the neural code. We recorded responses to moving visual stimuli from motion-sensitive neurons in the middle temporal area of anesthetized marmosets (Callithrix jacchus) and trained decoders to assess how correlated and uncorrelated populations encoded stimulus motion direction. We found that the most responsive, direction-selective, and least variable neurons are the most relied-upon neurons in an uncorrelated population. In correlated populations, the same neurons do the most to shape the shared variability across the population in a way that facilitates decoding, and decoding is improved by the presence of temporally stable correlations. This suggests that the least variable neurons with the strongest stimulus representations enhance the population code by providing a strong signal and shaping correlations in variability orthogonally to the locus defined by the mean response.

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Year:  2019        PMID: 29300838     DOI: 10.1093/cercor/bhx344

Source DB:  PubMed          Journal:  Cereb Cortex        ISSN: 1047-3211            Impact factor:   5.357


  8 in total

1.  Dendritic Spikes Expand the Range of Well Tolerated Population Noise Structures.

Authors:  Alon Poleg-Polsky
Journal:  J Neurosci       Date:  2019-09-26       Impact factor: 6.167

2.  A simple linear readout of MT supports motion direction-discrimination performance.

Authors:  Jacob L Yates; Leor N Katz; Aaron J Levi; Jonathan W Pillow; Alexander C Huk
Journal:  J Neurophysiol       Date:  2019-12-18       Impact factor: 2.714

3.  Information-Limiting Correlations in Large Neural Populations.

Authors:  Ramon Bartolo; Richard C Saunders; Andrew R Mitz; Bruno B Averbeck
Journal:  J Neurosci       Date:  2020-01-15       Impact factor: 6.167

4.  Motion Perception in the Common Marmoset.

Authors:  Shaun L Cloherty; Jacob L Yates; Dina Graf; Gregory C DeAngelis; Jude F Mitchell
Journal:  Cereb Cortex       Date:  2020-04-14       Impact factor: 5.357

5.  Axonal Projections From the Middle Temporal Area in the Common Marmoset.

Authors:  Hiroshi Abe; Toshiki Tani; Hiromi Mashiko; Naohito Kitamura; Taku Hayami; Satoshi Watanabe; Kazuhisa Sakai; Wataru Suzuki; Hiroaki Mizukami; Akiya Watakabe; Tetsuo Yamamori; Noritaka Ichinohe
Journal:  Front Neuroanat       Date:  2018-10-30       Impact factor: 3.856

6.  Contrast and luminance adaptation alter neuronal coding and perception of stimulus orientation.

Authors:  Masoud Ghodrati; Elizabeth Zavitz; Marcello G P Rosa; Nicholas S C Price
Journal:  Nat Commun       Date:  2019-02-26       Impact factor: 14.919

7.  Understanding Sensory Information Processing Through Simultaneous Multi-area Population Recordings.

Authors:  Elizabeth Zavitz; Nicholas S C Price
Journal:  Front Neural Circuits       Date:  2019-01-09       Impact factor: 3.492

8.  Visual response characteristics of neurons in the second visual area of marmosets.

Authors:  Yin Yang; Ke Chen; Marcello G P Rosa; Hsin-Hao Yu; Li-Rong Kuang; Jie Yang
Journal:  Neural Regen Res       Date:  2021-09       Impact factor: 5.135

  8 in total

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