Evidence map›Paper›PMID 15988029›Full record

ArticleMolecular and cellular biology2005

Loss of histochemical identity in mast cells lacking carboxypeptidase A.

Thorsten B Feyerabend, Heinz Hausser, Annette Tietz, Carmen Blum, Lars Hellman, Anita H Straus, Hélio K Takahashi, Ellen S Morgan, Ann M Dvorak, Hans Jörg Fehling and 1 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

42 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Enhanced Bone Remodeling After Fracture Priming.Calcified tissue international · 2022
    Article
  8. Review
  9. Mast Cell and Basophil Granule Proteases -Frontiers in immunology · 2022
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Mast cell proteases as pharmacological targets.European journal of pharmacology · 2016
    Review
  20. 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

11 authors at 5 institutions in 4 countries.

Thorsten B FeyerabendDepartment of Immunology, University of Ulm, D-89070 Ulm, Germany.
Heinz Hausser
Annette Tietz
Carmen Blum
Lars Hellman
Anita H Straus
Hélio K Takahashi
Ellen S Morgan
Ann M Dvorak
Hans Jörg Fehling
Hans-Reimer Rodewald
Universidade Federal de São Paulo · BRUniversität Ulm · DEBeth Israel Deaconess Medical Center · USHarvard University Press · USUppsala University · SE

Funding

BASOPHIL/MAST CELL FUNCTIONR01AI033372 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI DVORAK, ANN M · 1992 to 2004
$1.9M
NIAID NIH HHS AI33372NIAID NIH HHS R01 AI033372
6 · The paper itself

Abstract

Mast cell carboxypeptidase A (Mc-cpa) is a highly conserved secretory granule protease. The onset of expression in mast cell progenitors and lineage specificity suggest an important role for Mc-cpa in mast cells. To address the function of Mc-cpa, we generated Mc-cpa-null mice. Mc-cpa-/- mast cells lacked carboxypeptidase activity, revealing that Mc-cpa is a nonredundant enzyme. While Mc-cpa-/- peritoneal mast cells were ultrastructurally normal and synthesized normal amounts of heparin, they displayed striking histochemical and biochemical hallmarks of immature mast cells. Wild-type peritoneal mast cells had a mature phenotype characterized by differential histochemical staining with proteoglycan-reactive dyes (cells do not stain with alcian blue but stain with safranin and with berberine) and a high side scatter to forward scatter ratio by flow cytometry and were detergent resistant. In contrast, Mc-cpa-/- peritoneal mast cells, like immature bone marrow-derived cultured mast cells, stained with alcian blue normally or weakly and either did not stain with safranin and berberine or stained weakly, had a low side scatter to forward scatter ratio, and were detergent sensitive. This phenotype was partially ameliorated with age. Thus, histochemistry and flow cytometry, commonly used to measure mast cell maturation, deviated from morphology in Mc-cpa-/- mice. The Mc-cpa-/- mast cell phenotype was not associated with defects in degranulation in vitro or passive cutaneous anaphylaxis in vivo. Collectively, Mc-cpa plays a crucial role for the generation of phenotypically mature mast cells.

Indexed as

AnimalsAntibodiesBerberineCarboxypeptidases AHeparinHistocytochemistryMast CellsMiceMice, Mutant StrainsMonocyte Chemoattractant ProteinsPhenotypeProteoglycansSerine EndopeptidasesTryptasesAntibodiesBerberineCarboxypeptidases ACCL13 protein, humanCpa3 protein, mouseHeparinMonocyte Chemoattractant ProteinsProteoglycansSerine EndopeptidasesTpsab1 protein, mouseTpsb2 protein, mouseTryptases

Identifiers

PMID15988029
PMCPMC1168831
OpenAlexW2064815391

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.