Evidence map›Paper›PMID 31941925›Full record

ArticleNature communications2020

PI3KC2α-dependent and VPS34-independent generation of PI3P controls primary cilium-mediated autophagy in response to shear stress.

Asma Boukhalfa, Anna Chiara Nascimbeni, Damien Ramel, Nicolas Dupont, Emilio Hirsch, Stephanie Gayral, Muriel Laffargue, Patrice Codogno, Etienne Morel

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

44 citing papers in PubMed, 76 citations in OpenAlex.

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  8. Histone demethylases in autophagy and inflammation.Cell communication and signaling : CCS · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Asma BoukhalfaInstitut Necker-Enfants Malades (INEM), INSERM U1151 CNRS UMR 8253, Université Paris Descartes-Sorbonne Paris Cité, Paris, France.
Anna Chiara NascimbeniInstitut Necker-Enfants Malades (INEM), INSERM U1151 CNRS UMR 8253, Université Paris Descartes-Sorbonne Paris Cité, Paris, France.
Damien RamelInstitute of Metabolic and Cardiovascular Diseases, INSERM UMR 1048, Paul Sabatier University, Toulouse, France.ORCID http://orcid.org/0000-0002-9089-1497
Nicolas DupontInstitut Necker-Enfants Malades (INEM), INSERM U1151 CNRS UMR 8253, Université Paris Descartes-Sorbonne Paris Cité, Paris, France.
Emilio HirschMolecular Biotechnology Center, Department of Molecular Biotechnology and Health Sciences, University of Torino, Turin, Italy.ORCID http://orcid.org/0000-0002-9073-6024
Stephanie GayralInstitute of Metabolic and Cardiovascular Diseases, INSERM UMR 1048, Paul Sabatier University, Toulouse, France.
Muriel LaffargueInstitute of Metabolic and Cardiovascular Diseases, INSERM UMR 1048, Paul Sabatier University, Toulouse, France. muriel.laffargue@inserm.fr.
Patrice CodognoInstitut Necker-Enfants Malades (INEM), INSERM U1151 CNRS UMR 8253, Université Paris Descartes-Sorbonne Paris Cité, Paris, France. patrice.codogno@inserm.fr.
Etienne MorelInstitut Necker-Enfants Malades (INEM), INSERM U1151 CNRS UMR 8253, Université Paris Descartes-Sorbonne Paris Cité, Paris, France. etienne.morel@inserm.fr.ORCID http://orcid.org/0000-0002-4763-4954
Centre National de la Recherche Scientifique · FRUniversité Toulouse III - Paul Sabatier · FRDélégation Paris 5 · FRUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cells subjected to stress situations mobilize specific membranes and proteins to initiate autophagy. Phosphatidylinositol-3-phosphate (PI3P), a crucial lipid in membrane dynamics, is known to be essential in this context. In addition to nutriments deprivation, autophagy is also triggered by fluid-flow induced shear stress in epithelial cells, and this specific autophagic response depends on primary cilium (PC) signaling and leads to cell size regulation. Here we report that PI3KC2α, required for ciliogenesis and PC functions, promotes the synthesis of a local pool of PI3P upon shear stress. We show that PI3KC2α depletion in cells subjected to shear stress abolishes ciliogenesis as well as the autophagy and related cell size regulation. We finally show that PI3KC2α and VPS34, the two main enzymes responsible for PI3P synthesis, have different roles during autophagy, depending on the type of cellular stress: while VPS34 is clearly required for starvation-induced autophagy, PI3KC2α participates only in shear stress-dependent autophagy.

Indexed as

AnimalsAutophagyCell LineCell SizeCiliaClass III Phosphatidylinositol 3-KinasesGene Expression Regulation, EnzymologicGene Knockdown TechniquesHumansKidney Tubules, ProximalMice, Inbred C57BLMice, Mutant StrainsPhosphatidylinositol 3-KinasesPhosphatidylinositol PhosphatesStress, MechanicalClass III Phosphatidylinositol 3-KinasesPhosphatidylinositol 3-Kinasesphosphatidylinositol 3-phosphatePhosphatidylinositol PhosphatesPIK3C2A protein, humanPik3c2a protein, mousePIK3C3 protein, mouse

Identifiers

PMID31941925
PMCPMC6962367
OpenAlexW3000175340

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.