Evidence map›Paper›PMID 23363774›Full record

Trial reportJournal of innate immunity2013

Exocytosis of neutrophil granule subsets and activation of prolyl isomerase 1 are required for respiratory burst priming.

Kenneth R McLeish, Silvia M Uriarte, Shweta Tandon, Timothy M Creed, Junyi Le, Richard A Ward

Abstract readClinical Trial
In one paragraph

Trial report in Journal of innate immunity, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Observational
  6. The Hunger Games:Frontiers in immunology · 2021
    Article
  7. Review
  8. Article
  9. Therapeutic targeting of neutrophil exocytosis.Journal of leukocyte biology · 2020
    Review
  10. Human Neutrophil Granule Exocytosis in Response toPathogens (Basel, Switzerland) · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Endocytosis is required for exocytosis and priming of respiratory burst activity in human neutrophils.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2017
    Article
  15. Article
  16. Adenosine effectively restores endotoxin-induced inhibition of human neutrophil chemotaxis via A1 receptor-p38 pathway.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2017
    Article
  17. Multiple Phenotypic Changes Define Neutrophil Priming.Frontiers in cellular and infection microbiology · 2017
    Review
  18. Review
  19. Article
  20. Back to the Present.Journal of innate immunity · 2015
    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

6 authors at 1 institution in 1 country.

Kenneth R McLeishDepartment of Medicine, University of Louisville, Louisville, KY 40202, USA. k.mcleish@louisville.edu
Silvia M Uriarte
Shweta Tandon
Timothy M Creed
Junyi Le
Richard A Ward
University of Louisville · US

Funding

Granule exocytosis and neutrophil activationR00HL087924 · NHLBI · UNIVERSITY OF LOUISVILLE · PI URIARTE, SILVIA M · 2011 to 2013
$721k
Mechanism of Neutrophil ActivationI01BX001838 · VA · LOUISVILLE VA MEDICAL MEDICAL CENTER · PI MCLEISH, KENNETH R · 2013 to 2016
–
BLRD VA I01 BX001838NHLBI NIH HHS 4R00 HL087924NHLBI NIH HHS R00 HL087924
6 · The paper itself

Abstract

This study tested the hypothesis that priming the neutrophil respiratory burst requires both granule exocytosis and activation of the prolyl isomerase Pin1. Fusion proteins containing the TAT cell permeability sequence and either the SNARE domain of syntaxin-4 or the N-terminal SNARE domain of SNAP-23 were used to examine the role of granule subsets in TNF-mediated respiratory burst priming using human neutrophils. Concentration-inhibition curves for exocytosis of individual granule subsets and for priming of fMLF-stimulated superoxide release and phagocytosis-stimulated H2O2 production were generated. Maximal inhibition of priming ranged from 72 to 88%. Linear regression lines for inhibition of priming versus inhibition of exocytosis did not differ from the line of identity for secretory vesicles and gelatinase granules, while the slopes or the y-intercepts were different from the line of identity for specific and azurophilic granules. Inhibition of Pin1 reduced priming by 56%, while exocytosis of secretory vesicles and specific granules was not affected. These findings indicate that exocytosis of secretory vesicles and gelatinase granules and activation of Pin1 are independent events required for TNF-mediated priming of neutrophil respiratory burst.

Indexed as

Enzyme ActivationExocytosisFemaleHumansMaleNeutrophilsN-Formylmethionine Leucyl-PhenylalanineNIMA-Interacting Peptidylprolyl IsomerasePeptidylprolyl IsomeraseQa-SNARE ProteinsQb-SNARE ProteinsQc-SNARE ProteinsRespiratory BurstSecretory VesiclesTumor Necrosis Factor-alphaN-Formylmethionine Leucyl-PhenylalanineNIMA-Interacting Peptidylprolyl IsomerasePeptidylprolyl IsomerasePIN1 protein, humanQa-SNARE ProteinsQb-SNARE ProteinsQc-SNARE ProteinsSNAP23 protein, humanTumor Necrosis Factor-alpha

Identifiers

PMID23363774
PMCPMC3691856
OpenAlexW1981754471

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.