Evidence map›Paper›PMID 34848853›Full record

ArticleCell death and differentiation2022

Vinexin contributes to autophagic decline in brain ageing across species.

So Jung Park, Rebecca A Frake, Cansu Karabiyik, Sung Min Son, Farah H Siddiqi, Carla F Bento, Peter Sterk, Mariella Vicinanza, Mariana Pavel, David C Rubinsztein

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

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  12. IncreasedAutophagy · 2023
    Article
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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

10 authors at 1 institution in 2 countries.

So Jung Park *Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.
Rebecca A Frake *Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.ORCID http://orcid.org/0000-0003-2016-2368
Cansu KarabiyikCambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.
Sung Min SonCambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.
Farah H SiddiqiCambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.
Carla F BentoCambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.
Peter SterkCambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.
Mariella VicinanzaCambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.
Mariana PavelCambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.ORCID http://orcid.org/0000-0002-2802-5993
David C RubinszteinCambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK. dcr1000@cam.ac.uk.ORCID http://orcid.org/0000-0001-5002-5263
University of Cambridge · GB

Funding

Medical Research Council UKDRI-2002Wellcome TrustWellcome Trust 095317/Z/11/ZWellcome Trust 100140/Z/12/Z
6 · The paper itself

Abstract

Autophagic decline is considered a hallmark of ageing. The activity of this intracytoplasmic degradation pathway decreases with age in many tissues and autophagy induction ameliorates ageing in many organisms, including mice. Autophagy is a critical protective pathway in neurons and ageing is the primary risk factor for common neurodegenerative diseases. Here, we describe that autophagosome biogenesis declines with age in mouse brains and that this correlates with increased expression of the SORBS3 gene (encoding vinexin) in older mouse and human brain tissue. We characterise vinexin as a negative regulator of autophagy. SORBS3 knockdown increases F-actin structures, which compete with YAP/TAZ for binding to their negative regulators, angiomotins, in the cytosol. This promotes YAP/TAZ translocation into the nucleus, thereby increasing YAP/TAZ transcriptional activity and autophagy. Our data therefore suggest brain autophagy decreases with age in mammals and that this is likely, in part, mediated by increasing levels of vinexin.

Indexed as

Adaptor Proteins, Signal TransducingMuscle ProteinsTranscription FactorsAgingAnimalsAutophagyBrainHumansMammalsMicePhosphoproteinsYAP-Signaling ProteinsAdaptor Proteins, Signal TransducingMuscle ProteinsPhosphoproteinsSORBS3 protein, humanSorbs3 protein, mouseTranscription FactorsYAP-Signaling Proteins

Identifiers

PMID34848853
PMCPMC9090768
OpenAlexW3216292309

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.