Evidence map›Paper›PMID 16144798›Full record

ArticleBlood2006

Human and mouse mast cells use the tetraspanin CD9 as an alternate interleukin-16 receptor.

Jian C Qi, Jing Wang, Sravan Mandadi, Kumiko Tanaka, Basil D Roufogalis, Michele C Madigan, Kenneth Lai, Feng Yan, Beng H Chong, Richard L Stevens and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2006. 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
1.2field-weighted citation impact, top 21% 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, 79 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Cell Surface Proteins for Enrichment andStem cells international · 2022
    Article
  10. CD9, a tetraspanin target for cancer therapy?Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  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 4 institutions in 1 country.

Jian C QiDepartment of Medicine, University of New South Wales, Australia.
Jing Wang
Sravan Mandadi
Kumiko Tanaka
Basil D Roufogalis
Michele C Madigan
Kenneth Lai
Feng Yan
Beng H Chong
Richard L Stevens
Steven A Krilis
St George Hospital · AUSydney Hospital · AUUniversity of Sydney · AUUNSW Sydney · AU

Funding

Role of PGE2 in Human Mast Cell BiologyP01HL036110 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LAM, BING K · 1985 to 2009
$20.1M
RasGRP4-dependent Responses in Mast CellsR01AI054950 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI STEVENS, RICHARD L · 2005 to 2009
$2.0M
NHLBI NIH HHS HL036110NIAID NIH HHS AI054950
6 · The paper itself

Abstract

Interleukin-16 (IL-16) induces the chemotaxis and activation of mast cells (MCs) and other cell types. While it has been concluded that CD4 is the primary IL-16 receptor on T cells, at least one other IL-16 receptor exists. We now show that the IL-16-responsive human MC line HMC-1 lacks CD4, and that the IL-16-mediated chemotactic and Ca2+ mobilization responses of this cell can be blocked by anti-CD9 monoclonal antibodies (mAbs) but not by mAbs directed against CD4 or other tetraspanins. Anti-CD9 mAbs also inhibited the IL-16-mediated activation of nontransformed human cord blood-derived MCs and mouse bone marrow-derived MCs by 50% to 60%. The chemotactic response of HMC-1 cells to IL-16, as well as the binding of the cytokine to the cell's plasma membrane, was inhibited by CD9-specific antisense oligonucleotides. CD9 is therefore essential for the IL-16-mediated chemotaxis and activation of the HMC-1 cell line. In support of this conclusion, IL-16 bound to CD9-expressing CHO cell transfectants. The ability of wortmannin and xestopongin C to inhibit the IL-16-mediated chemotactic response of these cells suggests that the cytokine activates a phosphatidylinositol 3-kinase (PI3K)/inositol trisphosphate-dependent signaling pathway in MCs. This is the first report of a tetraspanin that plays a prominent role in a cytokine-mediated chemotactic response of human MCs.

Indexed as

AnimalsAntigens, CDBone Marrow CellsCalcium SignalingCells, CulturedChemotaxisFetal BloodHumansInterleukin-16Mast CellsMembrane GlycoproteinsMicePhosphatidylinositol 3-KinasesSignal TransductionTetraspanin 29Antigens, CDCD9 protein, humanCd9 protein, mouseInterleukin-16Membrane GlycoproteinsPhosphatidylinositol 3-KinasesTetraspanin 29

Identifiers

PMID16144798
PMCPMC1895361
OpenAlexW2110256102

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.