Evidence map›Paper›PMID 27244115›Full record

ArticleScientific reports2016

ALG-2 interacting protein-X (Alix) is essential for clathrin-independent endocytosis and signaling.

Vincent Mercier, Marine H Laporte, Olivier Destaing, Béatrice Blot, Cédric M Blouin, Karin Pernet-Gallay, Christine Chatellard, Yasmina Saoudi, Corinne Albiges-Rizo, Christophe Lamaze and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Enhanced insulin signaling via circulating ATG7: A potential therapeutic strategy for diabetes.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Review
  3. International journal of molecular sciences · 2024
    Article
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  5. Article
  6. Article
  7. Review
  8. Article
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  12. The Ins and Outs of Antigen Uptake in B cells.Frontiers in immunology · 2022
    Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Alix: A Candidate Serum Biomarker of Alzheimer's Disease.Frontiers in aging neuroscience · 2021
    Article
  18. Article
  19. Article
  20. Review
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

13 authors.

Vincent MercierInstitut National de la Santé et de la Recherche Médicale (INSERM), Unité 1216, F-38042 Grenoble, France.
Marine H LaporteInstitut National de la Santé et de la Recherche Médicale (INSERM), Unité 1216, F-38042 Grenoble, France.
Olivier DestaingINSERM U1209, Grenoble, F-38042, France.
Béatrice BlotInstitut National de la Santé et de la Recherche Médicale (INSERM), Unité 1216, F-38042 Grenoble, France.
Cédric M BlouinInstitut Curie, PSL Research University, Membrane Dynamics and Mechanics of Intracellular Signaling Laboratory, Paris, France.
Karin Pernet-GallayInstitut National de la Santé et de la Recherche Médicale (INSERM), Unité 1216, F-38042 Grenoble, France.
Christine ChatellardInstitut National de la Santé et de la Recherche Médicale (INSERM), Unité 1216, F-38042 Grenoble, France.
Yasmina SaoudiInstitut National de la Santé et de la Recherche Médicale (INSERM), Unité 1216, F-38042 Grenoble, France.
Corinne Albiges-RizoINSERM U1209, Grenoble, F-38042, France.
Christophe LamazeInstitut Curie, PSL Research University, Membrane Dynamics and Mechanics of Intracellular Signaling Laboratory, Paris, France.
Sandrine FrabouletInstitut National de la Santé et de la Recherche Médicale (INSERM), Unité 1216, F-38042 Grenoble, France.
Anne PetiotInstitut National de la Santé et de la Recherche Médicale (INSERM), Unité 1216, F-38042 Grenoble, France.
Rémy SadoulInstitut National de la Santé et de la Recherche Médicale (INSERM), Unité 1216, F-38042 Grenoble, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The molecular mechanisms and the biological functions of clathrin independent endocytosis (CIE) remain largely elusive. Alix (ALG-2 interacting protein X), has been assigned roles in membrane deformation and fission both in endosomes and at the plasma membrane. Using Alix ko cells, we show for the first time that Alix regulates fluid phase endocytosis and internalization of cargoes entering cells via CIE, but has no apparent effect on clathrin mediated endocytosis or downstream endosomal trafficking. We show that Alix acts with endophilin-A to promote CIE of cholera toxin and to regulate cell migration. We also found that Alix is required for fast endocytosis and downstream signaling of the interleukin-2 receptor giving a first indication that CIE is necessary for activation of at least some surface receptors. In addition to characterizing a new function for Alix, our results highlight Alix ko cells as a unique tool to unravel the biological consequences of CIE.

Indexed as

AcyltransferasesAnimalsB-LymphocytesCalcium-Binding ProteinsCell Cycle ProteinsCell Line, TumorCell MovementCholera ToxinClathrinEmbryo, MammalianEndocytosisEndosomal Sorting Complexes Required for TransportEndosomesFibroblastsGene ExpressionHumans2-acylglycerophosphate acyltransferaseAcyltransferasesCalcium-Binding ProteinsCell Cycle ProteinsCholera ToxinClathrinEndosomal Sorting Complexes Required for TransportPDCD6IP protein, humanPdcd6ip protein, mouseReceptors, Interleukin-2

Identifiers

PMID27244115
PMCPMC4886688

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Registered trials

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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.