Evidence map›Paper›PMID 18939952›Full record

ArticleTraffic (Copenhagen, Denmark)2008

The Rab27a effectors JFC1/Slp1 and Munc13-4 regulate exocytosis of neutrophil granules.

Agnieszka A Brzezinska, Jennifer L Johnson, Daniela B Munafo, Karine Crozat, Bruce Beutler, William B Kiosses, Beverly A Ellis, Sergio D Catz

Open access · bronzeAbstract read
In one paragraph

Article in Traffic (Copenhagen, Denmark), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

56 citing papers in PubMed, 89 citations in OpenAlex.

  1. Trial
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  11. Review
  12. Nexinhib20 Inhibits Neutrophil Adhesion and βJournal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Therapeutic targeting of neutrophil exocytosis.Journal of leukocyte biology · 2020
    Review
  18. Article
  19. Article
  20. Article
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 1 institution in 1 country.

Agnieszka A BrzezinskaDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Jennifer L Johnson
Daniela B Munafo
Karine Crozat
Bruce Beutler
William B Kiosses
Beverly A Ellis
Sergio D Catz
Scripps Research Institute · US

Funding

Vesicular trafficking mechanisms regulating granulocyte functionR01HL088256 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI Sergio Daniel Catz · 2009 to 2026
$9.0M
THE FUNCTION OF NORMAL AND MALIGNANT PHAGOCYTESR01AI024227 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI CATZ, SERGIO DANIEL · 1985 to 2007
$4.0M
FUNCTION OF NORMAL AND MALIGNANT PHAGOCYTESR37AI024227 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI BABIOR, BERNARD M · 1988 to 1997
–
NHLBI NIH HHS R01 HL088256NIAID NIH HHS AI-024227NIAID NIH HHS R01 AI024227
6 · The paper itself

Abstract

Neutrophil granules contain secretory molecules that contribute to the implementation of all neutrophil functions. The molecular components that regulate the exocytosis of neutrophil granules have not been characterized. In this study, using small interfering RNA gene-targeting approaches and granulocytes from genetically modified mice, we characterized the Rab27a effectors JFC1/Slp1 and Munc13-4 as components of the exocytic machinery of granulocytes. Using total internal reflection fluorescence microscopy analysis, we show that Rab27a and JFC1 colocalize in predocked and docked vesicles in granulocytes. Next, we demonstrate that JFC1-downregulated granulocytes have impaired myeloperoxidase secretion. Using immunological interference, we confirm that JFC1 plays an important role in azurophilic granule exocytosis in human neutrophils. Interference with Rab27a but not with JFC1 impaired gelatinase B secretion in neutrophils, suggesting that a different Rab27a effector modulates this process. In similar studies, we confirmed that Munc13-4 regulates gelatinase secretion. Immunofluorescence analysis indicates that Munc13-4 localizes at secretory organelles in neutrophils. Using neutrophils from a Munc13-4-deficient mouse model (Jinx), we demonstrate that Munc13-4 plays a central role in the regulation of exocytosis of various sets of secretory organelles. However, mobilization of CD11b was not affected in Munc13-4-deficient neutrophils, indicating that secretory defects in these cells are limited to a selective group of exocytosable organelles.

Indexed as

ExocytosisBase SequenceCells, CulturedCytoplasmic GranulesHumansMatrix Metalloproteinase 9Membrane ProteinsMicroscopy, Electron, TransmissionNeutrophilsrab27 GTP-Binding Proteinsrab GTP-Binding ProteinsRNA InterferenceVesicular Transport ProteinsMatrix Metalloproteinase 9Membrane ProteinsRAB27A protein, humanrab27 GTP-Binding Proteinsrab GTP-Binding ProteinsSYTL1 protein, humanUNC13D protein, humanVesicular Transport Proteins

Identifiers

PMID18939952
PMCPMC6363534
OpenAlexW2049727526

What OpenQuestion holds

Textmetadata
LicenceTDM
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.