Evidence map›Paper›PMID 34348156›Full record

ArticleCell reports2021

Disassembly and rewiring of a mature converging excitatory circuit following injury.

Luca Della Santina, Alfred K Yu, Scott C Harris, Manuel Soliño, Tonatiuh Garcia Ruiz, Jesse Most, Yien-Ming Kuo, Felice A Dunn, Yvonne Ou

Abstract read
In one paragraph

Article in Cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 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

9 authors.

Luca Della SantinaDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94158, USA; Bakar Computational Health Sciences Institute, University of California, San Francisco, San Francisco, CA 94158, USA. Electronic address: luca.dellasantina@ucsf.edu.
Alfred K YuDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94158, USA.
Scott C HarrisDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94158, USA; Neuroscience Graduate Program, University of California, San Francisco, San Francisco, CA 94158, USA.
Manuel SoliñoDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94158, USA.
Tonatiuh Garcia RuizDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94158, USA.
Jesse MostDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94158, USA.
Yien-Ming KuoDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94158, USA.
Felice A DunnDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94158, USA.
Yvonne OuDepartment of Ophthalmology, University of California, San Francisco, San Francisco, CA 94158, USA. Electronic address: yvonne.ou@ucsf.edu.

Funding

Rapid-Prototyping and Design CoreP30EY002162 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LAMBA, DEEPAK ASHOK · 1985 to 2024
$16.8M
Neuronal plasticity in glaucomaR01EY028148 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI OU, YVONNE · 2018 to 2022
$2.2M
NEI NIH HHS P30 EY002162NEI NIH HHS R01 EY028148
6 · The paper itself

Abstract

Specificity and timing of synapse disassembly in the CNS are essential to learning how individual circuits react to neurodegeneration of the postsynaptic neuron. In sensory systems such as the mammalian retina, synaptic connections of second-order neurons are known to remodel and reconnect in the face of sensory cell loss. Here we analyzed whether degenerating third-order neurons can remodel their local presynaptic connectivity. We injured adult retinal ganglion cells by transiently elevating intraocular pressure. We show that loss of presynaptic structures occurs before postsynaptic density proteins and accounts for impaired transmission from presynaptic neurons, despite no evidence of presynaptic cell loss, axon terminal shrinkage, or reduced functional input. Loss of synapses is biased among converging presynaptic neuron types, with preferential loss of the major excitatory cone-driven partner and increased connectivity with rod-driven presynaptic partners, demonstrating that this adult neural circuit is capable of structural plasticity while undergoing neurodegeneration.

Indexed as

AnimalsFemaleIntraocular PressureLightMaleMiceNerve NetPresynaptic TerminalsRetinal Bipolar CellsRetinal Ganglion CellsSynapsesWounds and InjuriesBipolar CellConvergenceExcitationNeurodegenerationPlasticityRetinal Ganglion CellRewiringRibbonSynapse

Identifiers

PMID34348156
PMCPMC8381591

What OpenQuestion holds

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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.