Evidence map›Paper›PMID 1493922›Full record

ArticleImmunology1992

Characterization of platelet-activating factor synthesized by normal and granulocyte-macrophage colony-stimulating factor-primed human eosinophils.

M Triggiani, R P Schleimer, K Tomioka, W C Hubbard, F H Chilton

Open access · greenAbstract read
In one paragraph

Article in Immunology, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Regulation and metabolism of arachidonic acid.Clinical reviews in allergy & immunology
    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

5 authors at 1 institution in 1 country.

M TriggianiDivision of Clinical Immunology, Johns Hopkins Asthma & Allergy Center, Baltimore, Maryland.
R P Schleimer
K Tomioka
W C Hubbard
F H Chilton
Allergy, Asthma and Clinical Research Center · US

Funding

ARACHIDONIC ACID LIBERATION AND REMODELING IN MAST CELLSR01AI024985 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CHILTON, FLOYD H · 1993 to 1997
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RELATIONSHIP BETWEEN PLATELET ACTIVATING FACTOR &EICOSAR01AI026771 · NIAID · WAKE FOREST UNIVERSITY · PI CHILTON, FLOYD H · 1988 to 1992
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GLUCOCORTICOSTEROID ACTION IN INFLAMMATORY DISEASER01AM031891 · AM · JOHNS HOPKINS UNIVERSITY · PI SCHLEIMER, ROBERT P · 1985 to 1985
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BIOCHEMICAL INTERACTIONS BETWEEN LIPID MEDIATOR CLASSESR29AI024985 · NIAID · WAKE FOREST UNIVERSITY · PI CHILTON, FLOYD H · 1988 to 1992
–
NIADDK NIH HHS AM 31891NIAID NIH HHS AI 24985NIAID NIH HHS AI 26771
6 · The paper itself

Abstract

Platelet-activating factor (PAF; 1-alkyl-2-acetyl-sn-glycero-3- phosphocholine) is a mediator involved in the pathogenesis of inflammatory diseases associated with tissue eosinophil infiltration. Previous studies utilizing bioassay or assaying enzymes associated with PAF biosynthesis have suggested that human eosinophils produce PAF. The present study has extended these initial studies by identifying and quantifying the different PAF molecular species and analogues synthesized by human eosinophils in response to A23187 and f-Met-Leu-Phe (FMLP). Gas chromatography-mass spectrometric analysis indicated that A23187-stimulated eosinophils produce at least three molecular species of PAF. The predominant species is 1-hexadecyl-2-acetyl-GPC (16:0) followed by 1-octadecyl-2-acetyl-GPC (18:0) and 1-octadecyl-2-acetyl-GPC (18:1). Eosinophils stimulated with FMLP produce approximately 100-fold smaller quantities of PAF relative to those produced in response to A23187 and only the 16:0 molecular species could be measured. A small percentage (comprising between 2 and 5%) of the 2-acetylated phospholipids produced by eosinophils was the 1-acyl analogue of PAF. Long-term (72 hr) incubation with granulocyte-macrophage colony-stimulating factor (GM-CSF) resulted in a three- to fourfold increase in PAF synthesis from eosinophils stimulated with FMLP, without changes in the profile of PAF molecular species or in the percentage of the 1-acyl analogue of PAF. These data indicate that human eosinophils can produce various molecular species of PAF and that this process can be quantitatively enhanced by GM-CSF.

Indexed as

CalcimycinCells, CulturedEosinophilsGranulocyte-Macrophage Colony-Stimulating FactorHumansN-Formylmethionine Leucyl-PhenylalaninePlatelet Activating FactorCalcimycinGranulocyte-Macrophage Colony-Stimulating FactorN-Formylmethionine Leucyl-PhenylalaninePlatelet Activating Factor

Identifiers

PMID1493922
PMCPMC1421661
OpenAlexW18924823

What OpenQuestion holds

Textmetadata
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.