Evidence map›Paper›PMID 23966624›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Transcriptional regulation of IL-15 expression during hematopoiesis.

Sara L Colpitts, Spencer W Stonier, Thomas A Stoklasek, Sierra H Root, Hector Leonardo Aguila, Kimberly S Schluns, Leo Lefrançois

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

40 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Splenic stromal niches in homeostasis and immunity.Nature reviews. Immunology · 2023
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Interleukin-15 in Outcomes of Pregnancy.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. IFNs Drive Development of Novel IL-15-Responsive Macrophages.Journal of immunology (Baltimore, Md. : 1950) · 2020
    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

7 authors at 2 institutions in 1 country.

Sara L ColpittsDepartment of Immunology, University of Connecticut Health Center, Farmington, CT 06030, USA.
Spencer W Stonier
Thomas A Stoklasek
Sierra H Root
Hector Leonardo Aguila
Kimberly S Schluns
Leo Lefrançois
UConn Health · USThe University of Texas MD Anderson Cancer Center · US

Funding

Training Program in Cancer ImmunobiologyT32CA009598 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ALLISON, JAMES P · 1988 to 2014
$4.9M
T Cell Response to Listeria Monocytogenes InfectionR01AI076457 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI SHERIDAN, BRIAN S · 2009 to 2019
$3.8M
Role of IL-15 in CD8 T Cell Development and ResponseR01AI051583 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LEFRANCOIS, LEO · 2002 to 2011
$3.1M
Role of TCRy& T cells in the mucosal response to intestinal infectionU01AI095544 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI KHANNA, KAMAL MOHAN · 2011 to 2015
$1.7M
Regulation of memory CD8 T Cell homeostasis by IL-15Ra+R01AI070910 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SCHLUNS, KIMBERLY SUE · 2006 to 2009
$1.5M
Osteoclasts from pluripotent stem cells as vectors to modify bone marrow environmRC1HL100569 · NHLBI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI AGUILA, HECTOR LEONARDO · 2010 to 2010
$792k
NCI NIH HHS CA009598NCI NIH HHS T32 CA009598NHLBI NIH HHS 1RC1HL100569NHLBI NIH HHS RC1 HL100569NIAID NIH HHS AI 070910NIAID NIH HHS R01 AI051583NIAID NIH HHS R01 AI070910NIAID NIH HHS R01 AI076457NIAID NIH HHS R01 AI76457NIAID NIH HHS U01 AI 095544NIAID NIH HHS U01 AI095544
6 · The paper itself

Abstract

Dendritic cells (DCs) are the most commonly studied source of the cytokine IL-15. Using an IL-15 reporter transgenic mouse, we have recently shown previously unappreciated differences in the levels of IL-15 expressed by subsets of conventional DCs (CD8⁺ and CD8⁻). In this study, we show that IL-15 promoter activity was differentially regulated in subsets of hematopoietically derived cells with IL-15 expression largely limited to myeloid lineages. In contrast, mature cells of the lymphoid lineages expressed little to no IL-15 activity. Surprisingly, we discovered that hematopoietic stem cells (lineage⁻Sca-1⁺c-Kit⁺) expressed high levels of IL-15, suggesting that IL-15 expression was extinguished during lymphoid development. In the case of T cells, this downregulation was Notch-dependent and occurred in a stepwise pattern coincident with increasing maturation and commitment to a T cell fate. Finally, we further demonstrate that IL-15 expression was also controlled throughout DC development, with key regulatory activity of IL-15 production occurring at the pre-DC branch point, leading to the generation of both IL-15⁺CD8⁺ and IL-15(⁻/low)CD8⁻ DC subsets. Thus, IL-15 expression is coordinated with cellular fate in myeloid versus lymphoid immune cells.

Indexed as

Adoptive TransferAnimalsCell DifferentiationCell LineageCell SeparationFlow CytometryGene Expression RegulationHematopoiesisHematopoietic Stem CellsInterleukin-15MiceMice, Inbred C57BLMice, TransgenicMyeloid CellsTranscription, GeneticInterleukin-15

Identifiers

PMID23966624
PMCPMC3896262
OpenAlexW2161170916

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.