Evidence map›Paper›PMID 28494703›Full record

ArticleVeterinary pathology2018

Globule Leukocytes and Other Mast Cells in the Mouse Intestine.

Peter Vogel, Laura Janke, David M Gravano, Meifen Lu, Deepali V Sawant, Dorothy Bush, E Shuyu, Dario A A Vignali, Asha Pillai, Jerold E Rehg

Open access · bronzeAbstract read
In one paragraph

Article in Veterinary pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

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  9. Article
  10. Tissue distribution of stem cell factor in adults.Experimental and molecular pathology · 2021
    Article
  11. Article
  12. Review
  13. Mast Cell Biology at Molecular Level: a Comprehensive Review.Clinical reviews in allergy & immunology · 2020
    Review
  14. Article
  15. Article
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  17. 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

10 authors at 4 institutions in 1 country.

Peter Vogel1 Department of Pathology, St Jude Children's Research Hospital, Memphis, TN, USA.
Laura Janke1 Department of Pathology, St Jude Children's Research Hospital, Memphis, TN, USA.
David M Gravano2 University of California Merced, Merced, CA, USA.
Meifen Lu1 Department of Pathology, St Jude Children's Research Hospital, Memphis, TN, USA.
Deepali V Sawant3 Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Dorothy Bush1 Department of Pathology, St Jude Children's Research Hospital, Memphis, TN, USA.
E Shuyu4 University of Miami School of Medicine, Miami, FL, USA.
Dario A A Vignali3 Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Asha Pillai4 University of Miami School of Medicine, Miami, FL, USA.
Jerold E Rehg1 Department of Pathology, St Jude Children's Research Hospital, Memphis, TN, USA.
St. Jude Children's Research Hospital · USUniversity of Miami · USUniversity of Pittsburgh · USUniversity of California, Merced · US

Funding

NOVEL INNATE MECHANISMS OF IMMUNE TOLERANCE INDUCTION IN ALLOGENEIC HCT FOR HEMOGLOBINOPATHIESR56HL125449 · NHLBI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PILLAI, ASHA BHASKARAN · 2015 to 2015
$446k
NHLBI NIH HHS R56 HL125449
6 · The paper itself

Abstract

Only 2 major mast cell (MC) subtypes are commonly recognized in the mouse: the large connective tissue mast cells (CTMCs) and the mucosal mast cells (MMCs). Interepithelial mucosal inflammatory cells, most commonly identified as globule leukocytes (GLs), represent a third MC subtype in mice, which we term interepithelial mucosal mast cells (ieMMCs). This term clearly distinguishes ieMMCs from lamina proprial MMCs (lpMMCs) while clearly communicating their common MC lineage. Both lpMMCs and ieMMCs are rare in normal mouse intestinal mucosa, but increased numbers of ieMMCs are seen as part of type 2 immune responses to intestinal helminth infections and in food allergies. Interestingly, we found that increased ieMMCs were consistently associated with decreased mucosal inflammation and damage, suggesting that they might have a role in controlling helminth-induced immunopathology. We also found that ieMMC hyperplasia can develop in the absence of helminth infections, for example, in Treg-deficient mice, Arf null mice, some nude mice, and certain graft-vs-host responses. Since tuft cell hyperplasia plays a critical role in type 2 immune responses to intestinal helminths, we looked for (but did not find) any direct relationship between ieMMC and tuft cell numbers in the intestinal mucosa. Much remains to be learned about the differing functions of ieMMCs and lpMMCs in the intestinal mucosa, but an essential step in deciphering their roles in mucosal immune responses will be to apply immunohistochemistry methods to consistently and accurately identify them in tissue sections.

Indexed as

AnimalsDisease Models, AnimalHelminthiasis, AnimalIntestinal MucosaIntestinesLeukocytesMast CellsMiceMice, Inbred BALB CMice, Inbred C57BLgraft-vs-hostHeligmosomoides bakeriimmunohistochemistrymast cellmouseTregTrichuris muris

Identifiers

PMID28494703
PMCPMC7732699
OpenAlexW2613973452

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.