Evidence map›Paper›PMID 34518644›Full record

ArticleLeukemia2022

Oncostatin M regulates hematopoietic stem cell (HSC) niches in the bone marrow to restrict HSC mobilization.

Kavita Bisht, Crystal McGirr, Seo-Youn Lee, Hsu-Wen Tseng, Whitney Fleming, Kylie A Alexander, Taichi Matsumoto, Valérie Barbier, Natalie A Sims, Gerhard Müller-Newen and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

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  12. Characterization of anbioRxiv : the preprint server for biology · 2023
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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

13 authors at 4 institutions in 3 countries.

Kavita BishtMater Research Institute-The University of Queensland, Woolloongabba, QLD, 4102, Australia.ORCID http://orcid.org/0000-0002-4073-0804
Crystal McGirrMater Research Institute-The University of Queensland, Woolloongabba, QLD, 4102, Australia.
Seo-Youn LeeGoethe University, Institute for Transfusion Medicine and Immunohematology, and German Red Cross Blood Donor Service Baden-Wuerttemberg-Hessen, Frankfurt, Germany.
Hsu-Wen TsengMater Research Institute-The University of Queensland, Woolloongabba, QLD, 4102, Australia.
Whitney FlemingMater Research Institute-The University of Queensland, Woolloongabba, QLD, 4102, Australia.
Kylie A AlexanderMater Research Institute-The University of Queensland, Woolloongabba, QLD, 4102, Australia.
Taichi MatsumotoMater Research Institute-The University of Queensland, Woolloongabba, QLD, 4102, Australia.
Valérie BarbierMater Research Institute-The University of Queensland, Woolloongabba, QLD, 4102, Australia.
Natalie A SimsSaint Vincent Institute, Fitzroy, VIC, 3065, Australia.ORCID http://orcid.org/0000-0003-1421-8468
Gerhard Müller-NewenInstitute of Biochemistry and Molecular Biology, RWTH Aachen University, Aachen, Germany.
Ingrid G WinklerMater Research Institute-The University of Queensland, Woolloongabba, QLD, 4102, Australia.ORCID http://orcid.org/0000-0001-6026-3572
Halvard BonigGoethe University, Institute for Transfusion Medicine and Immunohematology, and German Red Cross Blood Donor Service Baden-Wuerttemberg-Hessen, Frankfurt, Germany.
Jean-Pierre LévesqueMater Research Institute-The University of Queensland, Woolloongabba, QLD, 4102, Australia. jp.levesque@mater.uq.edu.au.ORCID http://orcid.org/0000-0002-7299-6025
The University of Queensland · AUGoethe University Frankfurt · DERWTH Aachen University · DESt Vincents Institute of Medical Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We show that pro-inflammatory oncostatin M (OSM) is an important regulator of hematopoietic stem cell (HSC) niches in the bone marrow (BM). Treatment of healthy humans and mice with granulocyte colony-stimulating factor (G-CSF) dramatically increases OSM release in blood and BM. Using mice null for the OSM receptor (OSMR) gene, we demonstrate that OSM provides a negative feed-back acting as a brake on HSPC mobilization in response to clinically relevant mobilizing molecules G-CSF and CXCR4 antagonist. Likewise, injection of a recombinant OSM molecular trap made of OSMR complex extracellular domains enhances HSC mobilization in poor mobilizing C57BL/6 and NOD.Cg-Prkdc

Indexed as

Stem Cell NicheAnimalsBone MarrowFemaleGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationHematopoietic Stem CellsHumansMaleMiceMice, Inbred C57BLMice, Inbred NODOncostatin MGranulocyte Colony-Stimulating FactorOncostatin M

Identifiers

PMID34518644
OpenAlexW3199515956

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.