Evidence map›Paper›PMID 26742601›Full record

ArticleNature communications2016

Haematopoietic ESL-1 enables stem cell proliferation in the bone marrow by limiting TGFβ availability.

Magdalena Leiva, Juan A Quintana, José M Ligos, Andrés Hidalgo

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. E3 ubiquitin ligase on the biological properties of hematopoietic stem cell.Journal of molecular medicine (Berlin, Germany) · 2023
    Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Hematopoietic stem cells under pressure.Current opinion in hematology · 2017
    Review
  11. Article
  12. Review
  13. Bidirectional dialog in the haematopoietic niche.Cell cycle (Georgetown, Tex.) · 2016
    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 1 institution in 2 countries.

Magdalena LeivaArea of Developmental and Cell Biology, Centro Nacional de Investigaciones Cardiovasculares, 28029 Madrid, Spain.
Juan A QuintanaArea of Developmental and Cell Biology, Centro Nacional de Investigaciones Cardiovasculares, 28029 Madrid, Spain.
José M LigosCellomics Unit, Centro Nacional de Investigaciones Cardiovasculares, 28029 Madrid, Spain.
Andrés HidalgoArea of Developmental and Cell Biology, Centro Nacional de Investigaciones Cardiovasculares, 28029 Madrid, Spain.ORCID http://orcid.org/0000-0001-5513-555X
Spanish National Centre for Cardiovascular Research · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The life-long maintenance of haematopoietic stem and progenitor cells (HSPCs) critically relies on environmental signals produced by cells that constitute the haematopoietic niche. Here we report a cell-intrinsic mechanism whereby haematopoietic cells limit proliferation within the bone marrow, and show that this pathway is repressed by E-selectin ligand 1 (ESL-1). Mice deficient in ESL-1 display aberrant HSPC quiescence, expansion of the immature pool and reduction in niche size. Remarkably, the traits were transplantable and dominant when mutant and wild-type precursors coexisted in the same environment, but were independent of E-selectin, the vascular receptor for ESL-1. Instead, quiescence is generated by unrestrained production of the cytokine TGFβ by mutant HSPC, and in vivo or in vitro blockade of the cytokine completely restores the homeostatic properties of the haematopoietic niche. These findings reveal that haematopoietic cells, including the more primitive compartment, can actively shape their own environment.

Indexed as

Cell ProliferationAnimalsBlotting, WesternBone MarrowChemokinesCytokinesFlow CytometryFluorescent Antibody TechniqueHematopoietic Stem CellsHomeostasisIn Vitro TechniquesMiceReal-Time Polymerase Chain ReactionReceptors, Fibroblast Growth FactorReverse Transcriptase Polymerase Chain ReactionSialoglycoproteinsChemokinescysteine-rich fibroblast growth factor receptorCytokinesReceptors, Fibroblast Growth FactorSialoglycoproteinsTgfb1 protein, mouseTransforming Growth Factor betaTransforming Growth Factor beta1

Identifiers

PMID26742601
PMCPMC4729861
OpenAlexW2269068265

What OpenQuestion holds

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LicenceCC BY
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.