Evidence map›Paper›PMID 23516351›Full record

ArticlePLoS computational biology2013

Directional summation in non-direction selective retinal ganglion cells.

Syed Y Abbas, Khaldoun C Hamade, Ellen J Yang, Scott Nawy, Robert G Smith, Diana L Pettit

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% of its field
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

5 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Short-term depression, temporal summation, and onset inhibition shape interval tuning in midbrain neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  5. 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

6 authors at 2 institutions in 1 country.

Syed Y AbbasDominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, New York, New York, USA.
Khaldoun C Hamade
Ellen J Yang
Scott Nawy
Robert G Smith
Diana L Pettit
Albert Einstein College of Medicine · USUniversity of Pennsylvania · US

Funding

MECHANISMS OF SYNAPTIC TRANSMISSION IN THE RETINAR01EY010254 · NEI · YESHIVA UNIVERSITY · PI NAWY, SCOTT · 1993 to 2013
$4.2M
Retinal circuits for precise signalingR01EY016607 · NEI · UNIVERSITY OF PENNSYLVANIA · PI SMITH, ROBERT G · 2006 to 2014
$2.7M
Inhibitory Microcircuits in the Piriform CortexR21DC010860 · NIDCD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI PETTIT, DIANA LESLIE · 2010 to 2011
$449k
NEI NIH HHS 1R01EY010254NEI NIH HHS 1R01EY016607NEI NIH HHS R01 EY010254NEI NIH HHS R01 EY016607NIDCD NIH HHS R21 DC010860NIDCD NIH HHS R21DC010860
6 · The paper itself

Abstract

Retinal ganglion cells receive inputs from multiple bipolar cells which must be integrated before a decision to fire is made. Theoretical studies have provided clues about how this integration is accomplished but have not directly determined the rules regulating summation of closely timed inputs along single or multiple dendrites. Here we have examined dendritic summation of multiple inputs along On ganglion cell dendrites in whole mount rat retina. We activated inputs at targeted locations by uncaging glutamate sequentially to generate apparent motion along On ganglion cell dendrites in whole mount retina. Summation was directional and dependent13 on input sequence. Input moving away from the soma (centrifugal) resulted in supralinear summation, while activation sequences moving toward the soma (centripetal) were linear. Enhanced summation for centrifugal activation was robust as it was also observed in cultured retinal ganglion cells. This directional summation was dependent on hyperpolarization activated cyclic nucleotide-gated (HCN) channels as blockade with ZD7288 eliminated directionality. A computational model confirms that activation of HCN channels can override a preference for centripetal summation expected from cell anatomy. This type of direction selectivity could play a role in coding movement similar to the axial selectivity seen in locust ganglion cells which detect looming stimuli. More generally, these results suggest that non-directional retinal ganglion cells can discriminate between input sequences independent of the retina network.

Indexed as

Models, NeurologicalAnimalsComputational BiologyCyclic Nucleotide-Gated Cation ChannelsDendritesGlutamatesHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsPhotochemical ProcessesPostsynaptic Potential SummationPotassium ChannelsPyrimidinesRatsRats, Sprague-DawleyRetinal Ganglion CellsCyclic Nucleotide-Gated Cation ChannelsGlutamatesHCN4 protein, ratHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsICI D2788Potassium ChannelsPyrimidines

Identifiers

PMID23516351
PMCPMC3597528
OpenAlexW2063702150

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.