Evidence map›Paper›PMID 31982451›Full record

ArticleThe Journal of allergy and clinical immunology2020

Charcot-Leyden crystal protein/galectin-10 interacts with cationic ribonucleases and is required for eosinophil granulogenesis.

Milica M Grozdanovic, Christine B Doyle, Li Liu, Brian T Maybruck, Mark A Kwatia, Nethaji Thiyagarajan, K Ravi Acharya, Steven J Ackerman

Open access · greenAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  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

8 authors at 2 institutions in 2 countries.

Milica M GrozdanovicDepartment of Biochemistry and Molecular Genetics, College of Medicine, University of Illinois at Chicago, Chicago, Ill.
Christine B DoyleDepartment of Biochemistry and Molecular Genetics, College of Medicine, University of Illinois at Chicago, Chicago, Ill.
Li LiuDepartment of Biochemistry and Molecular Genetics, College of Medicine, University of Illinois at Chicago, Chicago, Ill.
Brian T MaybruckDepartment of Biochemistry and Molecular Genetics, College of Medicine, University of Illinois at Chicago, Chicago, Ill.
Mark A KwatiaDepartment of Biochemistry and Molecular Genetics, College of Medicine, University of Illinois at Chicago, Chicago, Ill.
Nethaji ThiyagarajanDepartment of Biology and Biochemistry, University of Bath, Bath, United Kingdom.
K Ravi AcharyaDepartment of Biology and Biochemistry, University of Bath, Bath, United Kingdom.
Steven J AckermanDepartment of Biochemistry and Molecular Genetics, College of Medicine, University of Illinois at Chicago, Chicago, Ill. Electronic address: sackerma@uic.edu.
University of Illinois Chicago · USUniversity of Bath · GB

Funding

Structural Basis of Immune Recognition of Glycosylated AntigensU54GM062116 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI ALVAREZ, RICHARD · 2001 to 2010
$80.3M
Strengthening Stakeholder Engagement in Human Research Protections.UL1TR002003 · NCATS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KARNIK, NIRANJAN SUBHASH, MERMELSTEIN, ROBIN J. · 2016 to 2024
$33.7M
MOLECULAR BIOLOGY OF EOSINOPHIL AND BASOPHIL CLC PROTEINR01AI025230 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ACKERMAN, STEVEN JULES · 1987 to 2005
$2.2M
Training--Signal Transduction and Cellular EndocrinologyT32DK007739 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ACKERMAN, STEVEN JULES · 1997 to 2011
$1.5M
Role of Charcot-Leyden Crystal Protein in EosinophilsF32AI051137 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LIU, LI · 2002 to 2003
$111k
NCATS NIH HHS UL1 TR002003NIAID NIH HHS F32 AI051137NIAID NIH HHS R01 AI025230NIDDK NIH HHS T32 DK007739NIGMS NIH HHS U54 GM062116
6 · The paper itself

Abstract

backgroundThe human eosinophil Charcot-Leyden crystal (CLC) protein is a member of the Galectin superfamily and is also known as galectin-10 (Gal-10). CLC/Gal-10 forms the distinctive hexagonal bipyramidal crystals that are considered hallmarks of eosinophil participation in allergic responses and related inflammatory reactions; however, the glycan-containing ligands of CLC/Gal-10, its cellular function(s), and its role(s) in allergic diseases are unknown.

objectiveWe sought to determine the binding partners of CLC/Gal-10 and elucidate its role in eosinophil biology.

methodsIntracellular binding partners were determined by ligand blotting with CLC/Gal-10, followed by coimmunoprecipitation and coaffinity purifications. The role of CLC/Gal-10 in eosinophil function was determined by using enzyme activity assays, confocal microscopy, and short hairpin RNA knockout of CLC/Gal-10 expression in human CD34

resultsCLC/Gal-10 interacts with both human eosinophil granule cationic ribonucleases (RNases), namely, eosinophil-derived neurotoxin (RNS2) and eosinophil cationic protein (RNS3), and with murine eosinophil-associated RNases. The interaction is independent of glycosylation and is not inhibitory toward endoRNase activity. Activation of eosinophils with INF-γ induces the rapid colocalization of CLC/Gal-10 with eosinophil-derived neurotoxin/RNS2 and CD63. Short hairpin RNA knockdown of CLC/Gal-10 in human cord blood-derived CD34

conclusionsCLC/Gal-10 functions as a carrier for the sequestration and vesicular transport of the potent eosinophil granule cationic RNases during both differentiation and degranulation, enabling their intracellular packaging and extracellular functions in allergic inflammation.

Indexed as

AnimalsAntigens, CD34Cells, CulturedCytoplasmic GranulesEosinophil Cationic ProteinEosinophil-Derived NeurotoxinEosinophilsGalectinsGlycoproteinsGranulomaHematopoietic Stem CellsHumansHypersensitivityLysophospholipaseMiceProtein BindingAntigens, CD34Eosinophil Cationic ProteinEosinophil-Derived NeurotoxinGalectinsGlycoproteinslysolecithin acylhydrolaseLysophospholipaseCharcot-LeydenECPEDNEosinophilsgalectinsgranulogenesisribonucleasesRNase 2RNase 3

Identifiers

PMID31982451
PMCPMC7375938
OpenAlexW3002897773

What OpenQuestion holds

Textmetadata
LicenceTDM
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.