Evidence map›Paper›PMID 24781051›Full record

ArticleMucosal immunology2014

Impaired T-cell survival promotes mucosal inflammatory disease in SHIP1-deficient mice.

M Y Park, N Srivastava, R Sudan, D R Viernes, J D Chisholm, R W Engelman, W G Kerr

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

22 citing papers in PubMed, 38 citations in OpenAlex.

  1. SHIP1 is required for T cell surveillance of occult malignancies.Cellular and molecular life sciences : CMLS · 2026
    Article
  2. Article
  3. Genome-wide studies define new genetic mechanisms of IgA vasculitis.medRxiv : the preprint server for health sciences · 2024
    Article
  4. Article
  5. Pathological Roles of INPP5D in Alzheimer's Disease.Advances in experimental medicine and biology · 2023
    Article
  6. Article
  7. Synthetic studies on the indane SHIP1 agonist AQX-1125.Organic & biomolecular chemistry · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
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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

7 authors at 3 institutions in 1 country.

M Y Park *Dept. of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY, USA.
N Srivastava *Dept. of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY, USA.
R Sudan *Dept. of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY, USA.
D R ViernesDepartment of Chemistry, Syracuse University, Syracuse, NY, USA.
J D ChisholmDepartment of Chemistry, Syracuse University, Syracuse, NY, USA.
R W EngelmanDepts. of Pathology & Cell Biology, and Pediatrics, H. Lee Moffitt Comprehensive Cancer Center & Research Institute, University of South Florida, Tampa, FL, USA.
W G KerrDept. of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY, USA.
SUNY Upstate Medical University · USSyracuse University · USMoffitt Cancer Center · US

Funding

Role of SHIP in NK Cell BiologyR01HL072523 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI KERR, WILLIAM GARROW · 2002 to 2014
$4.3M
Chemical Inhibition of SHIP1 To Facilitate Allogeneic Bone Marrow TransplantationR01HL107127 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI KERR, WILLIAM GARROW · 2011 to 2014
$1.6M
SHIP and Immunoregulatory Cell FunctionR01HL085580 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI KERR, WILLIAM GARROW · 2008 to 2011
$1.5M
NHLBI NIH HHS R01 HL072523NHLBI NIH HHS R01 HL085580NHLBI NIH HHS R01 HL107127NHLBI NIH HHS R01 HL72523
6 · The paper itself

Abstract

T cells have a critical role in immune surveillance at mucosal surfaces. SHIP1(-/-) mice succumb to mucosal inflammatory disease that afflicts the lung and small intestine (SI). The basis of this condition has not been defined. Here we show that SHIP1 is required for the normal persistence and survival of T cells in mucosal tissues. We find that CD4 and CD8 effector T cells are reduced; however, Treg cells are increased in the SI and lungs of SHIP1(-/-) and CD4CreSHIP(flox/flox) mice. Furthermore, a subset of T cells in the SI of SHIP1(-/-) mice are FasL(+) and are more susceptible to extrinsic cell death. Mechanistic analyses showed that SHIP1 associates with the death receptor CD95/Fas and treatment with a Caspase 8 inhibitor prevents SHIP1 inhibitor-mediated T-cell death. Notably, mucosal inflammation in SHIP1(-/-) mice is reduced by treatment with a Caspase 8 inhibitor. We also find that the incidence of Crohn's disease (CD) and pneumonia is significantly increased in mice with dual T and myeloid lineage SHIP1 deletion but not in single lineage-deleted mice. Thus, by promoting survival of protective T cells, thereby preventing an inflammatory myeloid response, SHIP1 maintains an appropriate balance of innate immune function at mucosal surfaces necessary for immune homeostasis.

Indexed as

AnimalsCaspase 8Cell SurvivalCrohn DiseaseFas Ligand Proteinfas ReceptorInositol Polyphosphate 5-PhosphatasesIntestinal MucosaMiceMice, KnockoutPhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesPhosphoric Monoester HydrolasesPneumoniaRespiratory MucosaT-LymphocytesCasp8 protein, mouseCaspase 8Fas Ligand ProteinFasl protein, mousefas ReceptorInositol Polyphosphate 5-PhosphatasesInpp5d protein, mousePhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesPhosphoric Monoester Hydrolases

Identifiers

PMID24781051
PMCPMC4205272
OpenAlexW2007079192

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.