Evidence map›Paper›PMID 9435318›Full record

ArticleThe Journal of clinical investigation1998

Neutrophils exposed to bacterial lipopolysaccharide upregulate NADPH oxidase assembly.

F R DeLeo, J Renee, S McCormick, M Nakamura, M Apicella, J P Weiss, W M Nauseef

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 4% 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

109 citing papers in PubMed, 2 syntheses or guidelines pooled it, 313 citations in OpenAlex.

  1. NADPH oxidase p22phox C242T polymorphism and ischemic cerebrovascular disease: an updated meta-analysis.Medical science monitor : international medical journal of experimental and clinical research · 2015
    Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Sulfate Import inInfection and immunity · 2021
    Article
  19. Neutrophils in innate immunity and systems biology-level approaches.Wiley interdisciplinary reviews. Systems biology and medicine · 2020
    Article
  20. Review

49 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

7 authors at 3 institutions in 2 countries.

F R DeLeoDepartment of Medicine and the Inflammation Program, Veterans Administration Medical Center and University of Iowa, Iowa City, Iowa 52246, USA.
J Renee
S McCormick
M Nakamura
M Apicella
J P Weiss
W M Nauseef
University of Iowa · USNagasaki University · JPNew York University · US

Funding

RESEARCH TRAINING IN INFECTIOUS DISEASEST32AI007343 · NIAID · UNIVERSITY OF IOWA · PI STAPLETON, JACK T. · 1988 to 2024
$5.0M
MICROBICIDAL ACTIVITY OF LEUKOCYTES: MEMBRANE FACTORSR01DK005472 · NIDDK · UNIVERSITY OF IOWA · PI WEISS, JERROLD P · 1986 to 2002
$958k
Human neutrophils, phospholipase A2 and S.aureus: microbial targets and responsesI01BX000513 · VA · IOWA CITY VA MEDICAL CENTER · PI NAUSEEF, WILLIAM M. · 2009 to 2017
–
MICROBICIDAL ACTIVITY OF LEUKOCYTES: ACTIVE FACTORSR37DK005472 · NIDDK · NEW YORK UNIVERSITY · PI ELSBACH, PETER · 1987 to 1994
–
BLRD VA I01 BX000513NIAID NIH HHS 5-T32-AI07343-09NIAID NIH HHS AI-HL35879NIDDK NIH HHS DK05472
6 · The paper itself

Abstract

Bacterial LPS is a pluripotent agonist for PMNs. Although it does not activate the NADPH-dependent oxidase directly, LPS renders PMNs more responsive to other stimuli, a phenomenon known as "priming." Since the mechanism of LPS-dependent priming is incompletely understood, we investigated its effects on assembly and activation of the NADPH oxidase. LPS pretreatment increased superoxide (O2-) generation nearly 10-fold in response to N-formyl methionyl leucyl phenylalanine (fMLP). In a broken-cell O2--generating system, activity was increased in plasma membrane-rich fractions and concomitantly decreased in specific granule-rich fractions from LPS-treated cells. Oxidation-reduction spectroscopy and flow cytometry indicated LPS increased plasma membrane association of flavocytochrome b558. Immunoblots of plasma membrane vesicles from LPS-treated PMNs demonstrated translocation of p47-phox but not of p67-phox or Rac2. However, PMNs treated sequentially with LPS and fMLP showed a three- to sixfold increase (compared with either agent alone) in plasma membrane-associated p47-phox, p67-phox, and Rac2, and translocation paralleled augmented O2- generation by intact PMNs. LPS treatment caused limited phosphorylation of p47-phox, and plasma membrane-enriched fractions from LPS- and/or fMLP-treated cells contained fewer acidic species of p47-phox than did those from cells treated with PMA. Taken together, these studies suggest that redistribution of NADPH oxidase components may underlie LPS priming of the respiratory burst.

Indexed as

Cell MembraneCytochrome b GroupCytosolHumansLipopolysaccharidesNADPH OxidasesNeutrophilsN-Formylmethionine Leucyl-PhenylalaninePhosphoproteinsPhosphorylationRespiratory BurstSuperoxidescytochrome b558Cytochrome b GroupLipopolysaccharidesNADPH Oxidasesneutrophil cytosol factor 67Kneutrophil cytosolic factor 1N-Formylmethionine Leucyl-PhenylalaninePhosphoproteinsSuperoxides

Identifiers

PMID9435318
PMCPMC508585
OpenAlexW2065172724

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.