Evidence map›Paper›PMID 35430102›Full record

ReviewTrends in neurosciences2022

Intercellular signaling by ectodomain shedding at the synapse.

M Dolores Martín-de-Saavedra, Marc Dos Santos, Peter Penzes

Open access · greenAbstract readReview
In one paragraph

Review in Trends in neurosciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 22 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

3 authors at 3 institutions in 2 countries.

M Dolores Martín-de-SaavedraDepartment of Neuroscience, Northwestern University Feinberg School of Medicine, Chicago, 60611, IL, USA; Instituto Universitario de Investigación en Neuroquímica, Department of Biochemistry and Molecular Biology, School of Pharmacy, Complutense University of Madrid, 28040 Madrid, Spain.
Marc Dos SantosDepartment of Neuroscience, Northwestern University Feinberg School of Medicine, Chicago, 60611, IL, USA.
Peter PenzesDepartment of Neuroscience, Northwestern University Feinberg School of Medicine, Chicago, 60611, IL, USA; Northwestern Center for Autism and Neurodevelopment, Chicago, IL, USA; Department of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, Chicago, 60611, IL, USA; Department of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, 60611, IL, USA. Electronic address: p-penzes@northwestern.edu.
Center for Autism and Related Disorders · USNorthwestern University · USUniversidad Complutense de Madrid · ES

Funding

Synaptic and dendritic dysfunction in psychiatric disordersR01MH097216 · NIMH · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PENZES, PETER · 2012 to 2021
$6.1M
Postsynaptic functions of neuronal adhesion molecules: focus on Cntnap2R01NS100785 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PENZES, PETER · 2017 to 2020
$2.0M
Adhesion molecules and developmental epilepsy disordersR56NS100785 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PENZES, PETER · 2022 to 2022
$545k
NIMH NIH HHS R01 MH097216NINDS NIH HHS R01 NS100785NINDS NIH HHS R56 NS100785
6 · The paper itself

Abstract

Ectodomain shedding (ES) is a post-translational protein modification process that plays key roles in health and disease. Many neuronal and synaptic membrane proteins are known to undergo ES, but the complexity of functions regulated by the shed peptides is only beginning to be unraveled. Here, we provide an overview of emerging evidence demonstrating that synaptic ES can mediate autocrine and paracrine signaling. We also discuss how advances in large-scale proteomic analyses are leading to the identification of novel synaptic proteins undergoing ES, as well as the targets and functions of their soluble ectodomains. Finally, we provide an overview of how cerebrospinal fluid (CSF) analyses of shed proteins could be used as a potential source of new biomarkers for neuropsychiatric disorders.

Indexed as

ProteomicsSignal TransductionCell MembraneHumansMembrane ProteinsSynapsesMembrane Proteinsautismneurodegenerationplasticityproteomicssheddomesynapse

Identifiers

PMID35430102
PMCPMC9117472
OpenAlexW4224097730

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.