Evidence map›Paper›PMID 18499897›Full record

ArticleStem cells (Dayton, Ohio)2008

Hematopoietic stem cells regulate mesenchymal stromal cell induction into osteoblasts thereby participating in the formation of the stem cell niche.

Younghun Jung, Junhui Song, Yusuke Shiozawa, Jingcheng Wang, Zhuo Wang, Benjamin Williams, Aaron Havens, Abraham Schneider, Chunxi Ge, Renny T Franceschi and 3 more

Open access · greenAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

79 citing papers in PubMed, 168 citations in OpenAlex.

  1. Review
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  16. Bone marrow aspirate clot: A feasible orthobiologic.Journal of clinical orthopaedics and trauma · 2020
    Review
  17. Article
  18. Analysis of Hematopoietic Stem Progenitor Cell Metabolism.Journal of visualized experiments : JoVE · 2019
    Article
  19. Review
  20. Article

19 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Younghun JungDepartment of Periodontics & Oral Medicine, University of Michigan School of Dentistry, 1011 North University Avenue, Ann Arbor, Michigan 48109-1078, USA.
Junhui Song
Yusuke Shiozawa
Jingcheng Wang
Zhuo Wang
Benjamin Williams
Aaron Havens
Abraham Schneider
Chunxi Ge
Renny T Franceschi
Laurie K McCauley
Paul H Krebsbach
Russell S Taichman
University of Michigan–Ann Arbor · USUniversity of Maryland, Baltimore · US

Funding

Tumor microvesicle-mediated modulation of the bone microenvironmentP01CA093900 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KELLER, EVAN T · 2004 to 2024
$29.6M
YR01DE011723 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FRANCESCHI, RENNY THEODORE · 1995 to 2017
$5.3M
ANABOLIC MECHANISMS OF PTH ACTION IN BONER01DK053904 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MCCAULEY, LAURIE K. · 1998 to 2016
$4.6M
Pilot--Thrombospondin-2 regulation of MSC differentiationP30AR046024 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GOLDSTEIN, STEVEN A · 2001 to 2005
$3.0M
BONE MARROW STROMAL CELLS FOR SKELETAL REGENERATIONR01DE013835 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KREBSBACH, PAUL H · 2001 to 2005
$1.3M
Bone and the Hematopoietic SystemR01DE013701 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TAICHMAN, RUSSELL S · 2001 to 2004
$1.1M
MAP KINASE REGULATION OF OSTEOBLAST FUNCTIONR56DE011723 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FRANCESCHI, RENNY THEODORE · 2007 to 2007
$286k
Anabolic Mechanisms of PTH Action in BoneR56DK053904 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MCCAULEY, LAURIE K. · 2018 to 2018
$156k
NCI NIH HHS P01 CA093900NIAMS NIH HHS P30 AR046024NIDCR NIH HHS DE11723NIDCR NIH HHS DE13701NIDCR NIH HHS DE13835NIDCR NIH HHS R01 DE011723NIDCR NIH HHS R01 DE013701NIDCR NIH HHS R01 DE013835NIDCR NIH HHS R56 DE011723NIDDK NIH HHS DK53904NIDDK NIH HHS R01 DK053904NIDDK NIH HHS R56 DK053904
6 · The paper itself

Abstract

Crosstalk between hematopoietic stem cells (HSCs) and the cells comprising the niche is critical for maintaining stem cell activities. Yet little evidence supports the concept that HSCs regulate development of the niche. Here, the ability of HSCs to directly regulate endosteal development was examined. Marrow was isolated 48 hours after "stressing" mice with a single acute bleed or from control nonstressed animals. "Stressed" and "nonstressed" HSCs were cocultured with bone marrow stromal cells to map mesenchymal fate. The data suggest that HSCs are able to guide mesenchymal differentiation toward the osteoblastic lineage under basal conditions. HSCs isolated from animals subjected to an acute stress were significantly better at inducing osteoblastic differentiation in vitro and in vivo than those from control animals. Importantly, HSC-derived bone morphogenic protein 2 (BMP-2) and BMP-6 were responsible for these activities. Furthermore, significant differences in the ability of HSCs to generate a BMP response following stress were noted in aged and in osteoporotic animals. Together these data suggest a coupling between HSC functions and bone turnover as in aging and in osteoporosis. For the first time, these results demonstrate that HSCs do not rest passively in their niche. Instead, they directly participate in bone formation and niche activities. Disclosure of potential conflicts of interest is found at the end of this article.

Indexed as

AgingAnimalsBone DevelopmentBone Marrow CellsBone Morphogenetic ProteinsCell LineageCoculture TechniquesHematopoietic Stem CellsMesodermMiceMice, Inbred C57BLOsteoblastsOsteoporosisStem CellsStromal CellsBone Morphogenetic Proteins

Identifiers

PMID18499897
PMCPMC3513687
OpenAlexW2063626613

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.