Evidence map›Paper›PMID 24563081›Full record

ArticleInternational journal of hematology2014

Nov/CCN3 regulates long-term repopulating activity of murine hematopoietic stem cells via integrin αvβ3.

Jun Ishihara, Terumasa Umemoto, Masayuki Yamato, Yoshiko Shiratsuchi, Satoshi Takaki, Brian G Petrich, Hiromitsu Nakauchi, Koji Eto, Toshio Kitamura, Teruo Okano

Open access · greenAbstract read
In one paragraph

Article in International journal of hematology, 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
2.1field-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

22 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Inflammatory bone marrow microenvironment.Hematology. American Society of Hematology. Education Program · 2019
    Review
  10. Periostin function in communication with extracellular matrices.Journal of cell communication and signaling · 2018
    Review
  11. Review
  12. Introductory review: periostin-gene and protein structure.Cellular and molecular life sciences : CMLS · 2017
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Aortic aneurysm, CCN3 may solve the problem.Journal of thoracic disease · 2016
    Article
  18. The role of the CCN family of proteins in blood cancers.Journal of cell communication and signaling · 2016
    Article
  19. The role of CCN family genes in haematological malignancies.Journal of cell communication and signaling · 2015
    Article
  20. Come together, right now….Journal of cell communication and signaling · 2015
    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

10 authors at 5 institutions in 2 countries.

Jun IshiharaInstitute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, 8-1 Kawadacho, Shinjuku-ku, Tokyo, 162-8666, Japan.
Terumasa Umemoto
Masayuki Yamato
Yoshiko Shiratsuchi
Satoshi Takaki
Brian G Petrich
Hiromitsu Nakauchi
Koji Eto
Toshio Kitamura
Teruo Okano
Tokyo Women's Medical University · JPThe University of Tokyo · JPKyoto University · JPNational Center for Global Health and Medicine · JPUniversity of California, San Diego · US

Funding

Regulation of Platelet Integrin Signaling in Hemostasis and ThrombosisR01HL117061 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PETRICH, BRIAN G · 2013 to 2017
$1.7M
NHLBI NIH HHS R01 HL117061
6 · The paper itself

Abstract

Throughout life, hematopoietic stem cells (HSCs) sustain the blood cell supply through their capacities for self-renewal and multilineage differentiation. These processes are regulated within a specialized microenvironment termed the 'niche'. Here, we show a novel mechanism for regulating HSC function that is mediated by nephroblastoma overexpressed (Nov/CCN3), a matricellular protein member of the CCN family. We found that Nov contributes to the maintenance of long-term repopulating (LTR) activity through association with integrin αvβ3 on HSCs. The resultant β3 integrin outside-in signaling is dependent on thrombopoietin (TPO), a crucial cytokine involved in HSC maintenance. TPO was required for Nov binding to integrin αvβ3, and stimulated Nov expression in HSCs. However, in the presence of IFNγ, a cytokine known to impair HSC function, not only was TPO-induced expression of Nov suppressed, but the LTR activity was conversely impaired by TPO-mediated ligation of integrin αvβ3 with exogenous ligands, including Nov, as well. Thus, Nov/integrin αvβ3-mediated maintenance of HSCs appears to be modulated by simultaneous stimulation by other cytokines. Our finding suggests that this system contributes to the regulation of HSCs within the bone marrow niche.

Indexed as

AnimalsCell DifferentiationGene ExpressionHematopoietic Stem CellsHematopoietic Stem Cell TransplantationIntegrin alphaVbeta3Interferon-gammaMiceNephroblastoma Overexpressed ProteinSignal TransductionSTAT1 Transcription FactorThrombopoietinIntegrin alphaVbeta3Interferon-gammaNephroblastoma Overexpressed ProteinSTAT1 Transcription FactorThrombopoietin

Identifiers

PMID24563081
PMCPMC4412171
OpenAlexW2142129883

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.