Evidence map›Paper›PMID 7540656›Full record

ArticleThe Journal of experimental medicine1995

Differentiation in vitro of hybrid eosinophil/basophil granulocytes: autocrine function of an eosinophil developmental intermediate.

J A Boyce, D Friend, R Matsumoto, K F Austen, W F Owen

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
5.9field-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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 100 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Eosinophils and Mast Cells in Aspirin-Exacerbated Respiratory Disease.Immunology and allergy clinics of North America · 2016
    Review
  6. Review
  7. The Eosinophil in Health and Disease: from Bench to Bedside and Back.Clinical reviews in allergy & immunology · 2016
    Review
  8. Elements Involved In Promoting Eosinophilic Gastrointestinal Disorders.Journal of genetic syndromes & gene therapy · 2015
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Eosinophil survival and apoptosis in health and disease.Allergy, asthma & immunology research · 2010
    Article
  16. The clinical significance of eosinophils in the amniotic fluid in preterm labor.The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians · 2010
    Article
  17. The RBL-2H3 cell line: its provenance and suitability as a model for the mast cell.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2009
    Review
  18. Article
  19. Biology of the eosinophil.Advances in immunology · 2009
    Review
  20. Primary eosinophilic disorders: a concise review.Current hematologic malignancy reports · 2008
    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.

J A BoyceDepartment of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
D Friend
R Matsumoto
K F Austen
W F Owen
Harvard University · US

Funding

Role of PGE2 in Human Mast Cell BiologyP01HL036110 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI KATZ, HOWARD R · 1985 to 2009
$20.1M
MONOCYTE PHENOTYPES AND MORBIDITY IN UREMIAR01DK045656 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI OWEN, WILLIAM F · 1992 to 1996
–
URINARY AND EXCRETION OF LTR AS AN INDEX OF AIRWAY RESPONSESU01AI031599 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI OWEN, WILLIAM F · 1991 to 1994
–
THE V3 MASTOCYTOSIS MOUSE--MAST CELL DIFFERENTIATION, MATURATION, AND FUNCTIONU19AI031599 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI AUSTEN, K. FRANK · 1995 to 1998
–
NHLBI NIH HHS HL-36110NIAID NIH HHS AI-31599NIDDK NIH HHS DK-45656
6 · The paper itself

Abstract

Granulocytes with the hybrid characteristics of eosinophils and basophils have been identified in the bone marrow and peripheral blood of humans with myeloid leukemias. We now describe a technique by which such hybrid granulocytes can be developed in vitro from normal cord blood precursors cultured in the presence of recombinant human interleukin (rhIL) 3 (350 pM) and rhIL-5 (200 pM) in a plastic vessel coated with Matrigel. After 14 d in culture, 90 +/- 3% (mean +/- standard error of the mean) of the nonadherent cells cultured in the Matrigel-coated flasks contained both eosinophil and basophil granules, as indicated by staining with Wright's and Giemsa stains. Of the nonadherent cells, 93 +/- 1% contained cyanide-resistant peroxidase, and 88 +/- 2% were toluidine blue-positive, characteristic of eosinophil and basophil granules, respectively. Transmission electron micrographs showed hybrid cells containing ultrastructurally distinct eosinophil granules with developing crystalline cores and basophil granules with reticular structures. These 14-d cord blood-derived cell cultures showed strong hybridization signals for eosinophil-derived neurotoxin by RNA blot analysis and contained 78 ng histamine per 10(6) cells. When the granulocytes were removed from cytokine-containing medium and suspended without Matrigel in RPMI 1640 medium containing 10% fetal calf serum (FCS), more than 80% of the granulocytes excluded trypan blue for as long as 5 d, and 93% had developed into eosinophils at 6 d. Conditioned medium prepared over 48 h from the 14-d cell cultures (hybrid granulocytes) sustained the 4-d viability in vitro of 78% of peripheral blood eosinophils from atopic donors. In comparison, 13% survived in RPMI 1640 containing 10% FCS alone. This viability-sustaining activity was nearly completely neutralized by an anti-granulocyte/macrophage colony-stimulating factor (GM-CSF) antibody and was only minimally reduced by anti-IL-3 or IL-5. Thus, cells possessing both eosinophil and basophil granules by both histochemical and ultrastructural analysis can be developed from normal progenitors in vitro in response to eosinophilopoietic cytokines and Matrigel. Their subsequent spontaneous development into mature eosinophils suggests that hybrid granulocytes are part of a normal developmental sequence during eosinophilopoiesis. Furthermore, these hybrid granulocytes are capable of autoregulation through elaboration of GM-CSF, which sustains their viability.

Indexed as

RibonucleasesBiomarkersCell AdhesionCell DifferentiationCells, CulturedCell SeparationCollagenCulture Media, ConditionedCytoplasmic GranulesDrug CombinationsEosinophil-Derived NeurotoxinEosinophil PeroxidaseEosinophilsFetal BloodGranulocytesHematopoiesisBiomarkersCollagenCulture Media, ConditionedDrug CombinationsEosinophil-Derived NeurotoxinEosinophil PeroxidaseHistamineInterleukin-3Interleukin-5LamininmatrigelNeurotoxinsPeroxidasesProteoglycansRecombinant ProteinsRibonucleases

Identifiers

PMID7540656
PMCPMC2192091
OpenAlexW2005066469

What OpenQuestion holds

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LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

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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.