Evidence map›Paper›PMID 33459145›Full record

ArticleAutophagy2021

Decrease of neuronal FKBP4/FKBP52 modulates perinuclear lysosomal positioning and MAPT/Tau behavior during MAPT/Tau-induced proteotoxic stress.

Béatrice Chambraud, Corentin Daguinot, Kevin Guillemeau, Melanie Genet, Omar Dounane, Geri Meduri, Christian Poüs, Etienne Emile Baulieu, Julien Giustiniani

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

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  15. Autophagy and Tau Protein.International journal of molecular sciences · 2021
    Review
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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 at 1 institution in 1 country.

Béatrice ChambraudINSERM U1195, Université Paris-Saclay, Kremlin-Bicêtre, France.
Corentin DaguinotINSERM U1195, Université Paris-Saclay, Kremlin-Bicêtre, France.
Kevin GuillemeauINSERM U1195, Université Paris-Saclay, Kremlin-Bicêtre, France.
Melanie GenetINSERM U1195, Université Paris-Saclay, Kremlin-Bicêtre, France.
Omar DounaneINSERM U1195, Université Paris-Saclay, Kremlin-Bicêtre, France.
Geri MeduriINSERM U1195, Université Paris-Saclay, Kremlin-Bicêtre, France.
Christian PoüsINSERM UMR-S-1193, Université Paris-Saclay, Châtenay-Malabry, France.
Etienne Emile BaulieuINSERM U1195, Université Paris-Saclay, Kremlin-Bicêtre, France.
Julien GiustinianiINSERM U1195, Université Paris-Saclay, Kremlin-Bicêtre, France.ORCID 0000-0003-0373-5857
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defects of autophagy-lysosomal protein degradation are thought to contribute to the pathogenesis of several neurodegenerative diseases, and the accumulation of aggregation prone proteins such as MAPT/Tau in Alzheimer disease (AD). We previously showed the localization of the immunophilin FKBP4/FKBP52 in the lysosomal system of healthy human neurons suggesting its possible role in lysosome function. We also showed that decreased FKBP4 levels in AD brain neurons correlate with abnormal MAPT accumulation and aggregation. In this study, we demonstrate that FKBP4 decrease in a human neuronal cell line (SH-SY5Y) and in dorsal root ganglion (DRG) neurons from human MAPT

Indexed as

AgedAged, 80 and overAlzheimer DiseaseAnimalsAutophagyBrainCell LineCells, CulturedFemaleHumansLysosomesMaleMiceMice, TransgenicMicrotubule-Associated ProteinsMiddle AgedMAP1LC3A protein, humanMAPT protein, humanMicrotubule-Associated ProteinsSequestosome-1 ProteinSQSTM1 protein, humantacrolimus binding protein 4Tacrolimus Binding Proteinstau ProteinsAlzheimer diseaseautophagyFKBP52lysosomesproteotoxic stressTau

Identifiers

PMID33459145
PMCPMC8632305
OpenAlexW3126143611

What OpenQuestion holds

Textmetadata
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.