Evidence map›Paper›PMID 36346388›Full record

ArticleeLife2022

Spatiotemporal properties of glutamate input support direction selectivity in the dendrites of retinal starburst amacrine cells.

Prerna Srivastava, Geoff de Rosenroll, Akihiro Matsumoto, Tracy Michaels, Zachary Turple, Varsha Jain, Santhosh Sethuramanujam, Benjamin L Murphy-Baum, Keisuke Yonehara, Gautam Bhagwan Awatramani

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Compartmentalized pooling generates orientation selectivity in wide-field amacrine cells.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Optimization in Visual Motion Estimation.Annual review of vision science · 2024
    Review
  5. Neural Circuits Underlying Multifeature Extraction in the Retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

10 authors at 2 institutions in 2 countries.

Prerna Srivastava *Department of Biology, University of Victoria, Victoria, Canada.ORCID 0000-0002-3429-7039
Geoff de Rosenroll *Department of Biology, University of Victoria, Victoria, Canada.ORCID 0000-0002-5431-2814
Akihiro MatsumotoDanish Research Institute of Translational Neuroscience, Nordic-EMBL Partnership for Molecular Medicine, Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Tracy MichaelsDepartment of Biology, University of Victoria, Victoria, Canada.
Zachary TurpleDepartment of Biology, University of Victoria, Victoria, Canada.
Varsha JainDepartment of Biology, University of Victoria, Victoria, Canada.
Santhosh SethuramanujamDepartment of Biology, University of Victoria, Victoria, Canada.
Benjamin L Murphy-BaumDepartment of Biology, University of Victoria, Victoria, Canada.ORCID 0000-0001-6746-3091
Keisuke YoneharaDanish Research Institute of Translational Neuroscience, Nordic-EMBL Partnership for Molecular Medicine, Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Gautam Bhagwan AwatramaniDepartment of Biology, University of Victoria, Victoria, Canada.ORCID 0000-0002-0610-5271
University of Victoria · CAAarhus University · DK

Funding

CIHR 159444European Research Council 638730
6 · The paper itself

Abstract

The asymmetric summation of kinetically distinct glutamate inputs across the dendrites of retinal 'starburst' amacrine cells is one of the several mechanisms that have been proposed to underlie their direction-selective properties, but experimentally verifying input kinetics has been a challenge. Here, we used two-photon glutamate sensor (iGluSnFR) imaging to directly measure the input kinetics across individual starburst dendrites. We found that signals measured from proximal dendrites were relatively sustained compared to those measured from distal dendrites. These differences were observed across a range of stimulus sizes and appeared to be shaped mainly by excitatory rather than inhibitory network interactions. Temporal deconvolution analysis suggests that the steady-state vesicle release rate was ~3 times larger at proximal sites compared to distal sites. Using a connectomics-inspired computational model, we demonstrate that input kinetics play an important role in shaping direction selectivity at low stimulus velocities. Taken together, these results provide direct support for the 'space-time wiring' model for direction selectivity.

Indexed as

Amacrine CellsGlutamic AcidDendritesKineticsPhotonsGlutamic Acidbipolar cellsdirection selectivityiGluSnFRmouseneuroscienceretinal circuitryspace-time wiringstarburst amacrine cells

Identifiers

PMID36346388
PMCPMC9674338
OpenAlexW4308509969

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.