Evidence map›Paper›PMID 35196487›Full record

ArticleCell reports2022

Gain control by sparse, ultra-slow glycinergic synapses.

Varsha Jain, Laura Hanson, Santhosh Sethuramanujam, Tracy Michaels, Jerram Gawley, Ronald G Gregg, Ian Pyle, Chi Zhang, Robert G Smith, David Berson and 2 more

Abstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

12 authors.

Varsha JainDepartment of Biology, University of Victoria, Victoria, BC V8W 3N5 Canada.
Laura HansonDepartment of Biology, University of Victoria, Victoria, BC V8W 3N5 Canada.
Santhosh SethuramanujamDepartment of Biology, University of Victoria, Victoria, BC V8W 3N5 Canada.
Tracy MichaelsDepartment of Biology, University of Victoria, Victoria, BC V8W 3N5 Canada.
Jerram GawleyDepartment of Biology, University of Victoria, Victoria, BC V8W 3N5 Canada.
Ronald G GreggDepartment of Ophthalmology & Visual Sciences, University of Louisville, Louisville, KY 40202, USA.
Ian PyleDepartment of Anatomical Sciences & Neurobiology, University of Louisville, Louisville, KY 40202, USA.
Chi ZhangDepartment of Anatomical Sciences & Neurobiology, University of Louisville, Louisville, KY 40202, USA.
Robert G SmithDepartment of Neuroscience, University of Pennsylvania, Philadelphia, PA 19104, USA.
David BersonDepartment of Neuroscience, Brown University, Providence, RI 02912, USA.
Maureen A McCallDepartment of Ophthalmology & Visual Sciences, University of Louisville, Louisville, KY 40202, USA; Department of Anatomical Sciences & Neurobiology, University of Louisville, Louisville, KY 40202, USA. Electronic address: maureen.mccall@louisville.edu.
Gautam B AwatramaniDepartment of Biology, University of Victoria, Victoria, BC V8W 3N5 Canada. Electronic address: gautam@uvic.ca.

Funding

STRUCTURE AND FUNCTION OF MAMMALIAN GANGLION CELLSR01EY012793 · NEI · BROWN UNIVERSITY · PI BERSON, DAVID M. · 2000 to 2022
$9.3M
Ganglion Cell Function in Retinal DiseaseR01EY014701 · NEI · UNIVERSITY OF LOUISVILLE · PI MCCALL, MAUREEN A · 2004 to 2014
$3.5M
Retinal mechanisms for direction selectivityR01EY022070 · NEI · UNIVERSITY OF PENNSYLVANIA · PI SMITH, ROBERT G, TAYLOR, WILLIAM ROWLAND · 2012 to 2019
$2.8M
Glycine subunit specific inhibition and ganglion cell visual responsesR01EY029719 · NEI · UNIVERSITY OF LOUISVILLE · PI GREGG, RONALD G, MCCALL, MAUREEN A · 2019 to 2023
$2.6M
NEI NIH HHS R01 EY012793NEI NIH HHS R01 EY014701NEI NIH HHS R01 EY022070NEI NIH HHS R01 EY029719
6 · The paper itself

Abstract

In the retina, ON starburst amacrine cells (SACs) play a crucial role in the direction-selective circuit, but the sources of inhibition that shape their response properties remain unclear. Previous studies demonstrate that ∼95% of their inhibitory synapses are GABAergic, yet we find that the light-evoked inhibitory currents measured in SACs are predominantly glycinergic. Glycinergic inhibition is extremely slow, relying on non-canonical glycine receptors containing α4 subunits, and is driven by both the ON and OFF retinal pathways. These attributes enable glycine inputs to summate and effectively control the output gain of SACs, expanding the range over which they compute direction. Serial electron microscopic reconstructions reveal three specific types of ON and OFF narrow-field amacrine cells as the presumptive sources of glycinergic inhibition. Together, these results establish an unexpected role for specific glycinergic amacrine cells in the retinal computation of stimulus direction by SACs.

Indexed as

Amacrine CellsSynapsesGlycineRetinaGlycinealpha4 glycine receptorsdirection-selective ganglion celldirection selectivityGABA inhibitionGRAB-ACh3.0inhibitory neural circuitrynarrow-field amacrine cellsretinaserial block-face electron microscopystarburst amacrine cells

Identifiers

PMID35196487
PMCPMC8972185

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.