Evidence map›Paper›PMID 29212659›Full record

ArticleThe Journal of cell biology2018

Unconventional secretion of FABP4 by endosomes and secretory lysosomes.

Julien Villeneuve, Laia Bassaganyas, Sebastien Lepreux, Marioara Chiritoiu, Pierre Costet, Jean Ripoche, Vivek Malhotra, Randy Schekman

Abstract read
In one paragraph

Article in The Journal of cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
2.8field-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

61 citing papers in PubMed, 99 citations in OpenAlex.

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  9. Observational
  10. Review
  11. Endocytic tethers modulate unconventional GAPDH secretion.Cell surface (Amsterdam, Netherlands) · 2025
    Article
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  19. Canonical and noncanonical autophagy: involvement in Parkinson's disease.Frontiers in cell and developmental biology · 2025
    Review
  20. Review

1 more citing papers are in PubMed but not listed here.

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

8 authors at 5 institutions in 3 countries.

Julien VilleneuveCenter for Genomic Regulation, Barcelona Institute of Science and Technology, Barcelona, Spain.ORCID 0000-0002-5430-1680
Laia BassaganyasCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA.ORCID 0000-0002-4575-0214
Sebastien LepreuxInstitut National de la Santé et de la Recherche Médicale U1026, Université de Bordeaux, Bordeaux, France.
Marioara ChiritoiuCenter for Genomic Regulation, Barcelona Institute of Science and Technology, Barcelona, Spain.
Pierre CostetService des Animaleries, Université de Bordeaux, Bordeaux, France.
Jean RipocheInstitut National de la Santé et de la Recherche Médicale U1026, Université de Bordeaux, Bordeaux, France.
Vivek MalhotraCenter for Genomic Regulation, Barcelona Institute of Science and Technology, Barcelona, Spain vivek.malhotra@crg.eu.ORCID 0000-0001-6198-7943
Randy SchekmanDepartment of Molecular and Cell Biology and Howard Hughes Medical Institute, University of California, Berkeley, Berkeley, CA schekman@berkeley.edu.ORCID 0000-0001-8615-6409
Université de Bordeaux · FRHoward Hughes Medical Institute · USCentre for Genomic Regulation · ESInstitució Catalana de Recerca i Estudis Avançats · ESUniversity of California, San Francisco · US

Funding

A Zeiss Elyra S1 Structured Illumination Microscope for the Biological Imaging FaS10OD018136 · OD · UNIVERSITY OF CALIFORNIA BERKELEY · PI RUZIN, STEVEN EARL · 2014 to 2014
$600k
A Zeiss LSM 710 confocal microscope for the Biological Imaging Facility at the US10RR026866 · NCRR · UNIVERSITY OF CALIFORNIA BERKELEY · PI RUZIN, STEVEN EARL · 2010 to 2010
$419k
NCRR NIH HHS S10 RR026866NIH HHS S10 OD018136
6 · The paper itself

Abstract

An appreciation of the functional properties of the cytoplasmic fatty acid binding protein 4 (FABP4) has advanced with the recent demonstration that an extracellular form secreted by adipocytes regulates a wide range of physiological functions. Little, however, is known about the mechanisms that mediate the unconventional secretion of FABP4. Here, we demonstrate that FABP4 secretion is mediated by a membrane-bounded compartment, independent of the conventional endoplasmic reticulum-Golgi secretory pathway. We show that FABP4 secretion is also independent of GRASP proteins, autophagy, and multivesicular bodies but involves enclosure within endosomes and secretory lysosomes. We highlight the physiological significance of this pathway with the demonstration that an increase in plasma levels of FABP4 is inhibited by chloroquine treatment of mice. These findings chart the pathway of FABP4 secretion and provide a potential therapeutic means to control metabolic disorders associated with its dysregulated secretion.

Indexed as

3T3-L1 CellsAnimalsCells, CulturedEndosomesFatty Acid-Binding ProteinsLysosomesMiceMice, Inbred C57BLSecretory PathwayFabp4 protein, mouseFatty Acid-Binding Proteins

Identifiers

PMID29212659
PMCPMC5800802
OpenAlexW2774288517

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.