Evidence map›Paper›PMID 19228815›Full record

ArticleJournal of leukocyte biology2009

Endogenous suppression of mast cell development and survival by IL-4 and IL-10.

Kelly Speiran, Daniel P Bailey, Josephine Fernando, Matthew Macey, Brian Barnstein, Motunrayo Kolawole, Dana Curley, Stephanie S Watowich, Peter J Murray, Carole Oskeritzian and 1 more

Abstract read
In one paragraph

Article in Journal of leukocyte biology, 2009. 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
1.7field-weighted citation impact, top 16% 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, 49 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The mast cell: A Janus in kidney transplants.Frontiers in immunology · 2023
    Review
  5. Review
  6. Annexin A1 Mimetic Peptide AcFrontiers in immunology · 2021
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. IL-33/ST2 axis promotes mast cell survival via BCLXL.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  17. Article
  18. Article
  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

11 authors at 3 institutions in 1 country.

Kelly SpeiranAsthma and Allergic Disease Cooperative Research Center, Department of Biology, Virginia Commonwealth University, Richmond, VA 23284-2012, USA.
Daniel P Bailey
Josephine Fernando
Matthew Macey
Brian Barnstein
Motunrayo Kolawole
Dana Curley
Stephanie S Watowich
Peter J Murray
Carole Oskeritzian
John J Ryan
Virginia Commonwealth University · USSt. Jude Children's Research Hospital · USThe University of Texas MD Anderson Cancer Center · US

Funding

IL-10 Regulates Mast Cell Function and SurvivalR01AI059638 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI RYAN, JOHN J · 2007 to 2017
$3.8M
Sphingosine-1-Phosphate, A Novel Mediator of Human Skin Mass Cell FunctionsK01AR053186 · NIAMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI OSKERITZIAN, CAROLE A · 2006 to 2010
$522k
NIAID NIH HHS 1R01AI59638NIAID NIH HHS R01 AI059638NIAMS NIH HHS K01 AR053186NIAMS NIH HHS K01AR053186PHS HHS U191077435
6 · The paper itself

Abstract

Mast cell development is an important component of atopic and chronic inflammatory diseases such as asthma, multiple sclerosis, rheumatoid arthritis, and atherosclerosis. In this study, we found that IL-4 and IL-10 were produced constitutively in cultures of developing mast cells, correlating with mast cell purity. Deletion of either gene increased mast cell numbers and Fc epsilon RI expression during culture in IL-3 + stem cell factor (SCF). By adding exogenous IL-4 and IL-10 to bone marrow (BM) cultures containing IL-3 + SCF, we found that IL-4 + IL-10 suppressed mast cell development through mechanisms not used by either cytokine alone. IL-4 + IL-10 elicited a rapid cell death coincidental with reduced Kit receptor expression and signaling and enhanced mitochondrial damage and caspase activation. IL-4 or IL-10 costimulation, unlike either cytokine alone, altered mast cell ontogeny to yield predominantly macrophages in cultures that typically produce mast cells. This effect was observed consistently with unseparated BM cells, purified mouse BM stem cells, and erythrocyte-depleted human umbilical cord blood cells. These experiments demonstrated a major role for Stat6 and Stat3, but not the Stat3-induced transcriptional repressor Ets variant gene 3. Genetic background was also a critical factor, as BALB/c-derived BM cells were completely resistant to IL-10-mediated killing and expressed lower levels of IL-10R. Collectively, these results support the theory that IL-4 and IL-10 function as endogenous regulators of mast cell progenitor development, consistent with a role in immune homeostasis. Loss of this homeostasis, perhaps via genetic polymorphism, could contribute to the etiology of mast cell-associated disease.

Indexed as

AnimalsBone Marrow CellsCell DifferentiationCells, CulturedCell SurvivalHomeostasisHumansInterleukin-10Interleukin-4Mast CellsMiceMice, Inbred BALB CMice, Inbred C57BLRepressor ProteinsSTAT3 Transcription FactorSTAT6 Transcription FactorETV3 protein, mouseInterleukin-10Interleukin-4Repressor ProteinsStat3 protein, mouseSTAT3 Transcription FactorStat6 protein, mouseSTAT6 Transcription Factor

Identifiers

PMID19228815
PMCPMC2669408
OpenAlexW2099558832

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.