Evidence map›Paper›PMID 22048767›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

Lineage(-)Sca1+c-Kit(-)CD25+ cells are IL-33-responsive type 2 innate cells in the mouse bone marrow.

Adipong Brickshawana, Virginia Smith Shapiro, Hirohito Kita, Larry R Pease

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Theranostics · 2021
    Article
  3. Article
  4. Article
  5. Article
  6. Interleukin-33 and ST2 Signaling in Tumor Microenvironment.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2019
    Review
  7. Review
  8. Article
  9. Adenosine receptors differentially regulate type 2 cytokine production by IL-33-activated bone marrow cells, ILC2s, and macrophages.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Mast cells mediate malignant pleural effusion formation.The Journal of clinical investigation · 2015
    Article
  17. Article
  18. Review
  19. Article
  20. 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

4 authors at 2 institutions in 1 country.

Adipong BrickshawanaDepartment of Immunology, Mayo Clinic, Rochester, MN 55905, USA.
Virginia Smith Shapiro
Hirohito Kita
Larry R Pease
Mayo Clinic in Arizona · USWinnMed · US

Funding

Type 2 Innate Lymphoid Cells and AsthmaR01HL117823 · NHLBI · MAYO CLINIC ROCHESTER · PI KITA, HIROHITO · 2014 to 2021
$3.5M
NHLBI NIH HHS R01 HL117823
6 · The paper itself

Abstract

IL-33 promotes type 2 immune responses, both protective and pathogenic. Recently, targets of IL-33, including several newly discovered type 2 innate cells, have been characterized in the periphery. In this study, we report that bone marrow cells from wild-type C57BL/6 mice responded with IL-5 and IL-13 production when cultured with IL-33. IL-33 cultures of bone marrow cells from Rag1 KO and Kit(W-sh/W-sh) mice also responded similarly; hence, eliminating the possible contributions of T, B, and mast cells. Rather, intracellular staining revealed that the IL-5- and IL-13-positive cells display a marker profile consistent with the Lineage(-)Sca-1(+)c-Kit(-)CD25(+) (LSK(-)CD25(+)) cells, a bone marrow cell population of previously unknown function. Freshly isolated LSK(-)CD25(+) cells uniformly express ST2, the IL-33 receptor. In addition, culture of sorted LSK(-)CD25(+) cells showed that they indeed produce IL-5 and IL-13 when cultured with IL-33 plus IL-2 and IL-33 plus IL-7. Furthermore, i.p. injections of IL-33 or IL-25 into mice induced LSK(-)CD25(+) cells to expand, in both size and frequency, and to upregulate ST2 and α(4)β(7) integrin, a mucosal homing marker. Thus, we identify the enigmatic bone marrow LSK(-)CD25(+) cells as IL-33 responsive, both in vitro and in vivo, with attributes similar to other type 2 innate cells described in peripheral tissues.

Indexed as

AnimalsAntigens, LyBone Marrow CellsCell LineageCell SeparationCytokinesFlow CytometryImmunity, InnateInterleukin-2 Receptor alpha SubunitInterleukin-33InterleukinsMaleMembrane ProteinsMiceMice, Inbred C57BLMice, KnockoutAntigens, LyCytokinesIl2ra protein, mouseIl33 protein, mouseInterleukin-2 Receptor alpha SubunitInterleukin-33InterleukinsLy6a protein, mouseMembrane ProteinsProto-Oncogene Proteins c-kit

Identifiers

PMID22048767
PMCPMC4449734
OpenAlexW2141528748

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.