Evidence map›Paper›PMID 27558339›Full record

ReviewImmunological reviews2016

Molecular mechanisms regulating secretory organelles and endosomes in neutrophils and their implications for inflammation.

Mahalakshmi Ramadass, Sergio D Catz

Abstract readReview
In one paragraph

Review in Immunological reviews, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Neutrophils and Anesthetic Drugs: Implications in Onco-Anesthesia.International journal of molecular sciences · 2024
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. The role of neutrophils in chorioamnionitis.Frontiers in immunology · 2023
    Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  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

2 authors.

Mahalakshmi RamadassDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA, USA.
Sergio D CatzDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA, USA.

Funding

Vesicular trafficking mechanisms regulating granulocyte functionR01HL088256 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI Sergio Daniel Catz · 2009 to 2026
$9.0M
Modulators of granulocyte regulated secretion for control of inflammationR01GM105894 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI CATZ, SERGIO DANIEL, ROSEN, HUGH · 2013 to 2015
$1.1M
NHLBI NIH HHS R01 HL088256NIGMS NIH HHS R01 GM105894
6 · The paper itself

Abstract

Neutrophils constitute the first line of cellular defense against invading microorganisms and modulate the subsequent innate and adaptive immune responses. In order to execute a rapid and precise response to infections, neutrophils rely on preformed effector molecules stored in a variety of intracellular granules. Neutrophil granules contain microbicidal factors, the membrane-bound components of the respiratory burst oxidase, membrane-bound adhesion molecules, and receptors that facilitate the execution of all neutrophil functions including adhesion, transmigration, phagocytosis, degranulation, and neutrophil extracellular trap formation. The rapid mobilization of intracellular organelles is regulated by vesicular trafficking mechanisms controlled by effector molecules that include small GTPases and their interacting proteins. In this review, we focus on recent discoveries of mechanistic processes that are at center stage of the regulation of neutrophil function, highlighting the discrete and selective pathways controlled by trafficking modulators. In particular, we describe novel pathways controlled by the Rab27a effectors JFC1 and Munc13-4 in the regulation of degranulation, reactive oxygen species and neutrophil extracellular trap production, and endolysosomal signaling. Finally, we discuss the importance of understanding these molecular mechanisms in order to design novel approaches to modulate neutrophil-mediated inflammatory processes in a targeted fashion.

Indexed as

PhagocytosisAnimalsCell DegranulationEndosomesHumansInflammationMembrane ProteinsNeutrophilsProtein Transportrab27 GTP-Binding Proteinsrab GTP-Binding ProteinsSecretory VesiclesMembrane ProteinsRAB27A protein, humanrab27 GTP-Binding Proteinsrab GTP-Binding ProteinsSYTL1 protein, humanUNC13D protein, humaninflammationneutrophil functionRab GTPasevesicular trafficking

Identifiers

PMID27558339
PMCPMC6363536

What OpenQuestion holds

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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.