Evidence map›Paper›PMID 1562046›Full record

ArticleThe American journal of pathology1992

Mature eosinophils stimulated to develop in human-cord blood mononuclear cell cultures supplemented with recombinant human interleukin-5. II. Vesicular transport of specific granule matrix peroxidase, a mechanism for effecting piecemeal degranulation.

A M Dvorak, S J Ackerman, T Furitsu, P Estrella, L Letourneau, T Ishizaka

Open access · greenAbstract read
In one paragraph

Article in The American journal of pathology, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 66 citations in OpenAlex.

  1. Eosinophils: old cells, new directions.Frontiers in medicine · 2024
    Review
  2. Review
  3. The Enigma of Eosinophil Degranulation.International journal of molecular sciences · 2021
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Vesicle-mediated secretion of human eosinophil granule-derived major basic protein.Laboratory investigation; a journal of technical methods and pathology · 2009
    Article
  9. Article
  10. Review
  11. Mechanisms of eosinophilia in the pathogenesis of hypereosinophilic disorders.Immunology and allergy clinics of North America · 2007
    Review
  12. Article
  13. Mechanisms of eosinophil cytokine release.Memorias do Instituto Oswaldo Cruz · 2005
    Review
  14. Article
  15. Article
  16. 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 1 institution in 1 country.

A M DvorakDepartment of Pathology, Beth Israel Hospital, Boston, MA 02215.
S J Ackerman
T Furitsu
P Estrella
L Letourneau
T Ishizaka
Beth Israel Deaconess Hospital · US

Funding

BIOCHEMICAL RELATIONSHIPS OF BASOPHILS AND EOSINOPHILSR01AI022660 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ACKERMAN, STEVEN JULES · 1986 to 1990
–
BASOPHIL/MAST CELL FUNCTION IN THE CONTROL OF CANCERR01CA028834 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI DVORAK, ANN M · 1985 to 1991
–
NCI NIH HHS CA 28834NIAID NIH HHS AI 10060NIAID NIH HHS AI 22660
6 · The paper itself

Abstract

The mechanism of piecemeal degranulation by human eosinophils was investigated. Mature eosinophils that developed in rhIL-5-containing conditioned media from cultured human cord blood mononuclear cells were prepared for ultrastructural studies using a combined technique to image eosinophil peroxidase by cytochemistry in the same sections on which postembedding immunogold was used to demonstrate Charcot-Leyden crystal protein. Vesicular transport of eosinophil peroxidase from the specific granule matrix compartment to the cell surface was associated with piecemeal degranulation. This process involved budding of eosinophil peroxidase-loaded vesicles and tubules from specific granules. Some eosinophil peroxidase that was released from eosinophils remained bound to the cell surface; some was free among the cultured cells. Macrophages and basophils bound the released eosinophil peroxidase to their plasma membranes, internalized it in endocytotic vesicles, and stored it in their respective phagolysosomes and secretory granules. Charcot-Leyden crystal protein was diffusely present in the nucleus and cytoplasm of IL-5-stimulated mature eosinophils. Extensive amounts were generally present in granule-poor and subplasma membrane areas of the cytoplasm in contrast to eosinophil peroxidase, which was secreted and bound to the external surface of eosinophil plasma membranes. These studies establish vesicular transport as a mechanism for emptying the specific eosinophil granule matrix compartment during IL-5-associated piecemeal degranulation.

Indexed as

Fetal BloodBlood CellsCells, CulturedCellular SenescenceCytoplasmic GranulesEosinophilsGlycoproteinsHumansInterleukin-5LysophospholipaseMonocytesPeroxidasesRecombinant ProteinsTissue DistributionGlycoproteinsInterleukin-5lysolecithin acylhydrolaseLysophospholipasePeroxidasesRecombinant Proteins

Identifiers

PMID1562046
PMCPMC1886371
OpenAlexW200289249

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.