Evidence map›Paper›PMID 15947420›Full record

ArticleAmerican journal of respiratory cell and molecular biology2005

Allergic challenge-elicited lipid bodies compartmentalize in vivo leukotriene C4 synthesis within eosinophils.

Adriana Vieira-de-Abreu, Edson F Assis, Gleice S Gomes, Hugo C Castro-Faria-Neto, Peter F Weller, Christianne Bandeira-Melo, Patrícia T Bozza

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 56 citations in OpenAlex.

  1. A mechanism of benefit of soy genistein in asthma: inhibition of eosinophil p38-dependent leukotriene synthesis.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2008
    Trial
  2. IL-33 Elicits LTCEuropean journal of immunology · 2026
    Article
  3. Article
  4. Article
  5. Inflammasome-Independent Leukotriene BJournal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. LEUKOCYTE LIPID BODIES - STRUCTURE AND FUNCTION AS "EICOSASOMES".Transactions of the American Clinical and Climatological Association · 2016
    Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
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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 1 institution in 1 country.

Adriana Vieira-de-AbreuLaboratorio de Imunofarmacologia, Departamento de Fisiologia e Farmacodinâmica, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz; Av. Brasil 4365, Manguinhos 21045-900 Rio de Janeiro, RJ Brazil.
Edson F Assis
Gleice S Gomes
Hugo C Castro-Faria-Neto
Peter F Weller
Christianne Bandeira-Melo
Patrícia T Bozza
Fundação Oswaldo Cruz · BR

Funding

CYTOPLASMIC LIPID BODIES OF INFLAMMATORY CELLSR01AI022571 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WELLER, PETER F · 1985 to 2013
$4.5M
Eosinophil Lipid Bodies in Allergic InflammationR03TW005890 · FIC · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WELLER, PETER F · 2002 to 2004
$117k
FIC NIH HHS TW 05890NIAID NIH HHS AI 22571
6 · The paper itself

Abstract

Eosinophils are an important source of leukotriene (LT)C(4), which can be synthesized within lipid bodies-cytoplasmic organelles where eicosanoid formation may take place. Allergy-driven lipid body formation and function have never been investigated. Here, we studied the in vivo induction and role of lipid bodies within eosinophils recruited to sites of allergic inflammation. Using two murine models of allergic inflammation (asthma and pleurisy), we verified that parallel to the eosinophil influx, allergic challenge also induced lipid body formation within recruited eosinophils. Neutralizing antibodies to eotaxin/CCL11, RANTES/CCL5, or CCR3 partially inhibited lipid body formation within recruited eosinophils in the allergic pleurisy model. Likewise, intrapleural administration of RANTES or eotaxin also induced significant influx of eosinophils loaded with lipid bodies. By immunolabeling, we detected the presence of a key enzyme involved in the leukotriene metabolism-5-lipoxygenase-within eosinophil lipid bodies formed in vivo after allergen challenge. Furthermore, specific immunolocalization of newly formed LTC(4) demonstrated that lipid bodies were the sites of formation of this eicosanoid within infiltrating eosinophils. Therefore, allergic inflammation triggers in vivo formation of new lipid bodies within infiltrating eosinophils, a phenomenon largely mediated by eotaxin/RANTES acting via CCR3 receptors. Such in vivo allergen-driven lipid bodies function as intracellular compartments of LTC(4) synthesis.

Indexed as

Lipid MetabolismAnimalsArachidonate 5-LipoxygenaseCell CompartmentationChemokine CCL11Chemokine CCL5Chemokines, CCChemotaxis, LeukocyteEosinophilsFemaleLeukotriene C4LipidsMaleMiceMice, Inbred C57BLPleurisyArachidonate 5-LipoxygenaseCcl11 protein, mouseChemokine CCL11Chemokine CCL5Chemokines, CCLeukotriene C4Lipids

Identifiers

PMID15947420
PMCPMC2715315
OpenAlexW2013623558

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.