Evidence map›Paper›PMID 25597631›Full record

ArticleNature communications2015

Annexin A2 promotes phagophore assembly by enhancing Atg16L⁺ vesicle biogenesis and homotypic fusion.

Kateryna Morozova, Sunandini Sridhar, Sunandini Sidhar, Valerio Zolla, Cristina C Clement, Brian Scharf, Zoe Verzani, Antonio Diaz, Jorge N Larocca, Katherine A Hajjar and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
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  14. Extracellular vesicles fromFrontiers in immunology · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Annexin Animal Models-From Fundamental Principles to Translational Research.International journal of molecular sciences · 2021
    Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Kateryna MorozovaDepartment of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, New York 10461, USA.
Sunandini SridharDepartment of Developmental Molecular Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, New York 10461, USA.
Sunandini SidharDepartment of Developmental Molecular Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, New York 10461, USA.
Valerio ZollaDepartment of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, New York 10461, USA.
Cristina C ClementDepartment of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, New York 10461, USA.
Brian ScharfDepartment of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, New York 10461, USA.
Zoe Verzani1] Department of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, New York 10461, USA [2] Department of Cell and Developmental Biology, Weill Cornell Medical College, 1300 York Avenue, New York, New York 10065, USA.
Antonio DiazDepartment of Developmental Molecular Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, New York 10461, USA.
Jorge N LaroccaDepartment of Neurology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, New York 10461, USA.
Katherine A Hajjar1] Department of Cell and Developmental Biology, Weill Cornell Medical College, 1300 York Avenue, New York, New York 10065, USA [2] Department of Pediatrics, Weill Cornell Medical College, 1300 York Avenue, New York, New York 10065, USA.
Ana Maria CuervoDepartment of Developmental Molecular Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, New York 10461, USA.
Laura Santambrogio1] Department of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, New York 10461, USA [2] Department of Microbiology and Immunology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, New York 10461, USA.
Albert Einstein College of Medicine · USCornell University · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
Role of Autophagy in T Cell Function and Immunosenescence (Project 3)P01AG031782 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MACIAN, FERNANDO · 2009 to 2024
$36.2M
Special Animal CoreP30DK041296 · NIDDK · YESHIVA UNIVERSITY · PI WOLKOFF, ALLAN W · 1989 to 2018
$22.9M
Core-010UL1TR001073 · NCATS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI KELLER, MARLA J, SHAMOON, HARRY · 2013 to 2017
$21.3M
Einstein's Nathan Shock Center of Excellence in Basic Biology of AgingP30AG038072 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CUERVO, ANA MARIA · 2010 to 2024
$10.8M
Regulation of Endothelial Cell Function in AngiogenesisP01HL067839 · NHLBI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI RAFII, SHAHIN · 2001 to 2005
$6.7M
NEW THROMBOREGULATORY PROTEIN, ANNEXIN IIR01HL042493 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI HAJJAR, KATHERINE AMBERSON · 1989 to 2016
$4.9M
MHC class II-restricted immune response in immunosenescenceR01AG045223 · NIA · WEILL MEDICAL COLL OF CORNELL UNIV · PI SANTAMBROGIO, LAURA · 2014 to 2018
$1.7M
MASS SPECTROMETER SYSTEM: OBESITYS10RR019352 · NCRR · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI ANGELETTI, RUTH HOGUE · 2004 to 2004
$379k
NCATS NIH HHS UL1 TR001073NCI NIH HHS P30 CA013330NCRR NIH HHS 1S10RR019352NCRR NIH HHS S10 RR019352NHLBI NIH HHS HL042493NHLBI NIH HHS P01 HL067839NHLBI NIH HHS R01 HL042493NIA NIH HHS AG031782NIA NIH HHS P01 AG031782NIA NIH HHS P30 AG038072NIA NIH HHS R01 AG045223NIDDK NIH HHS P30 DK041296
6 · The paper itself

Abstract

Plasma membrane budding of Atg-16L-positive vesicles represents a very early event in the generation of the phagophore and in the process of macroautophagy. Here we show that the membrane curvature-inducing protein annexin A2 contributes to the formation of these vesicles and their fusion to form phagophores. Ultrastructural, proteomic and FACS analyses of Atg16L-positive vesicles reveal that 30% of Atg16L-positive vesicles are also annexin A2-positive. Lipidomic analysis of annexin A2-deficient mouse cells indicates that this protein plays a role in recruiting phosphatidylserine and phosphatidylinositides to Atg16L-positive vesicles. Absence of annexin A2 reduces both vesicle formation and homotypic Atg16L vesicle fusion. Ultimately, a reduction in LC3 flux and dampening of macroautophagy are observed in dendritic cells from Anxa2(-/-) mice. Together, our analyses highlight the importance of annexin A2 in vesiculation of a population of Atg16L-positive structures from the plasma membrane, and in their homotypic fusion to form phagophore structures.

Indexed as

AnimalsAnnexin A2Carrier ProteinsCell MembraneDendritic CellsFemaleFlow CytometryMiceMice, Inbred C57BLMicroscopy, Electron, TransmissionPhagosomesProtein TransportAnnexin A2Carrier Proteins

Identifiers

PMID25597631
PMCPMC4299943
OpenAlexW1995291945

What OpenQuestion holds

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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.