Evidence map›Paper›PMID 19171875›Full record

ArticleBlood2009

Mature human eosinophils express functional Notch ligands mediating eosinophil autocrine regulation.

Amy L Radke, Lauren E Reynolds, Rossana C N Melo, Ann M Dvorak, Peter F Weller, Lisa A Spencer

Open access · greenAbstract read
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Notch signaling pathway: architecture, disease, and therapeutics.Signal transduction and targeted therapy · 2022
    Review
  8. Review
  9. Article
  10. Multi-Faceted Notch in Allergic Airway Inflammation.International journal of molecular sciences · 2019
    Review
  11. Review
  12. Review
  13. Review
  14. Notch signaling in lung diseases: focus on Notch1 and Notch3.Therapeutic advances in respiratory disease · 2016
    Review
  15. The Regulatory Function of Eosinophils.Microbiology spectrum · 2016
    Review
  16. Increased risk for the development of preeclampsia in obese pregnancies: weighing in on the mechanisms.American journal of physiology. Regulatory, integrative and comparative physiology · 2015
    Review
  17. Article
  18. Article
  19. Article
  20. Human eosinophils express functional CCR7.American journal of respiratory cell and molecular biology · 2013
    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 2 institutions in 2 countries.

Amy L RadkeDepartment of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Lauren E Reynolds
Rossana C N Melo
Ann M Dvorak
Peter F Weller
Lisa A Spencer
Harvard University · USBeth Israel Deaconess Medical Center · US

Funding

CYTOPLASMIC LIPID BODIES OF INFLAMMATORY CELLSR01AI022571 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WELLER, PETER F · 1985 to 2013
$4.5M
Human Eosinophils: Mechanisms of FunctioningR37AI020241 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WELLER, PETER F · 2010 to 2019
$4.5M
Airways Eosinophils as Antigen-presenting Cells in AsthmaR01AI051645 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WELLER, PETER F · 2001 to 2011
$3.8M
HUMAN EOSINOPHILS: MECHANISMS OF FUNCTIONINGR01AI020241 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WELLER, PETER F · 1985 to 2009
$3.5M
Notch signaling-mediated functions of airway eosinophils in lung diseaseR01HL095699 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SPENCER, LISA ANN · 2010 to 2014
$2.1M
NHLBI NIH HHS R01 HL095699NIAID NIH HHS AI020241NIAID NIH HHS AI051645NIAID NIH HHS R01 AI020241NIAID NIH HHS R01 AI022571NIAID NIH HHS R01 AI051645NIAID NIH HHS R37 AI020241
6 · The paper itself

Abstract

Eosinophil chemotaxis and survival within tissues are key components in the development of tissue eosinophilia and subsequent effector responses. In this study, we demonstrate a novel mechanism of eosinophil autoregulation affecting migration and survival mediated through Notch signaling. We show for the first time that human blood eosinophils express Notch receptors and Notch ligands, expressions of which are influenced by the presence of eosinophil-activating granulocyte-macrophage colony-stimulating factor (GM-CSF). Evidence of Notch receptor activation and subsequent transcription of the Notch-responsive gene HES1 were observed in GM-CSF-stimulated eosinophils, confirming functionality of eosinophil-expressed Notch-signaling components. Moreover, by inhibiting Notch signaling with gamma-secretase inhibitors or Notch receptor-specific neutralizing antibodies, we demonstrate that autocrine Notch signaling enhances stimulus-mediated actin rearrangement and eosinophil chemokinesis, and impairs eosinophil viability. Taken together, these data suggest autocrine Notch signaling, enhanced in response to tissue- or inflammatory-derived signals, influences eosinophil activity and longevity, which may ultimately contribute to the development of tissue eosinophilia and exacerbation or remediation of eosinophil effector functions.

Indexed as

LigandsAutocrine CommunicationCalcium-Binding ProteinsCell DifferentiationCells, CulturedCell SurvivalEndopeptidasesEnzyme InhibitorsEosinophilsGene Expression RegulationGranulocyte-Macrophage Colony-Stimulating FactorHumansIntercellular Signaling Peptides and ProteinsIntracellular Signaling Peptides and ProteinsJagged-2 ProteinMembrane ProteinsAPH1A protein, humanCalcium-Binding Proteinsdelta proteinEndopeptidasesEnzyme InhibitorsGranulocyte-Macrophage Colony-Stimulating FactorIntercellular Signaling Peptides and ProteinsIntracellular Signaling Peptides and ProteinsJAG2 protein, humanJagged-2 ProteinLigandsMembrane ProteinsPeptide HydrolasesReceptors, NotchSerrate-Jagged ProteinsSoluble N-Ethylmaleimide-Sensitive Factor Attachment Proteins

Identifiers

PMID19171875
PMCPMC2662649
OpenAlexW2055095585

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.