Evidence map›Paper›PMID 35108533›Full record

ArticleCell reports2022

Inhibition, but not excitation, recovers from partial cone loss with greater spatiotemporal integration, synapse density, and frequency.

Joo Yeun Lee, Rachel A Care, David B Kastner, Luca Della Santina, Felice A Dunn

Open access · goldAbstract 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-weighted citation impact, top 15% 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, 21 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Joo Yeun LeeDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94143-0518, USA. Electronic address: jooyeun.lee@ucsf.edu.
Rachel A CareDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94143-0518, USA.
David B KastnerDepartment of Psychiatry and Behavioral Sciences, University of California, San Francisco, San Francisco, CA 94143-0518, USA.
Luca Della SantinaDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94143-0518, USA; Bakar Computational Health Science Institute, University of California, San Francisco, San Francisco, CA 94143-0518, USA.
Felice A DunnDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94143-0518, USA. Electronic address: felice.dunn@ucsf.edu.
University of California, San Francisco · US

Funding

Rapid-Prototyping and Design CoreP30EY002162 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LAMBA, DEEPAK ASHOK · 1985 to 2024
$16.8M
Synaptic and circuit mechanisms of compensation following loss of cone inputs in the mature retinaR01EY029772 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Felice A Dunn · 2019 to 2026
$3.7M
NEI NIH HHS P30 EY002162NEI NIH HHS R01 EY029772
6 · The paper itself

Abstract

Neural circuits function in the face of changing inputs, either caused by normal variation in stimuli or by cell death. To maintain their ability to perform essential computations with partial inputs, neural circuits make modifications. Here, we study the retinal circuit's responses to changes in light stimuli or in photoreceptor inputs by inducing partial cone death in the mature mouse retina. Can the retina withstand or recover from input loss? We find that the excitatory pathways exhibit functional loss commensurate with cone death and with some aspects predicted by partial light stimulation. However, inhibitory pathways recover functionally from lost input by increasing spatiotemporal integration in a way that is not recapitulated by partially stimulating the control retina. Anatomically, inhibitory synapses are upregulated on secondary bipolar cells and output ganglion cells. These findings demonstrate the greater capacity for inhibition, compared with excitation, to modify spatiotemporal processing with fewer cone inputs.

Indexed as

AnimalsMiceRetinaRetinal Cone Photoreceptor CellsRetinal Ganglion CellsRetinal Rod Photoreceptor CellsSynapsesVisual Pathwayscellular and systems neurosciencedegenerationdiseaseganglion cellshomeostatic plasticityperceptionphotoreceptorsreceptive fieldretinavision

Identifiers

PMID35108533
PMCPMC8865908
OpenAlexW4226424761

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.