Evidence map›Paper›PMID 25164953›Full record

ArticleJournal of cellular biochemistry2015

The bone marrow endosteal niche: how far from the surface?

Eric Cordeiro-Spinetti, Russell S Taichman, Alex Balduino

Abstract read
In one paragraph

Article in Journal of cellular biochemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. 3DACS biomaterials science & engineering · 2026
    Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Autophagic Mediators in Bone Marrow Niche Homeostasis.Advances in experimental medicine and biology · 2022
    Article
  8. Interactions of Hematopoietic Stem Cells with Bone Marrow Niche.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. A T Cell View of the Bone Marrow.Frontiers in immunology · 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

3 authors.

Eric Cordeiro-SpinettiCell Technology and Biology Lab, Veiga de Almeida University, Rio de Janeiro, 20270-150, RJ, Brazil.
Russell S Taichman
Alex Balduino

Funding

Tumor microvesicle-mediated modulation of the bone microenvironmentP01CA093900 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PIENTA, KENNETH J. · 2004 to 2024
$29.6M
Pilot--Thrombospondin-2 regulation of MSC differentiationP30AR046024 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GOLDSTEIN, STEVEN A · 2001 to 2005
$3.0M
Mechanisms That Regulate Dormancy of Disseminated Tumor Cells in the Bone MarrowU54CA163124 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PIENTA, KENNETH J. · 2011 to 2015
$3.0M
Repair of Bone Defects with Human Autologous Pluripotent Very Small Embryonic likR44DE022493 · NIDCR · LISATA THERAPEUTICS INC · PI MCCAULEY, LAURIE K., RODGERSON, DENIS OVEREND · 2012 to 2012
$412k
Repair of boney defects by human stem cellsR43AR056893 · NIAMS · LISATA THERAPEUTICS INC · PI RODGERSON, DENIS OVEREND, TAICHMAN, RUSSELL S · 2009 to 2009
$109k
NCI NIH HHS CA093900NCI NIH HHS U54 CA163124NIAMS NIH HHS P30 AR046024NIAMS NIH HHS R43 AR056893NIDCR NIH HHS R44 DE022493
6 · The paper itself

Abstract

Hematopoietic stem cells (HSC) self-renewal takes place in the same microenvironment in which massive hematopoietic progenitor proliferation, commitment, and differentiation will occur. This is only made possible if the bone marrow microenvironment comprises different specific niches, composed by different stromal cells that work in harmony to regulate all the steps of the hematopoiesis cascade. Histological and functional assays indicated that HSC and multipotent progenitors preferentially colonize the endosteal and subendosteal regions, in close association with the bone surface. Conversely, committed progenitors and differentiated cells are distributed in the central and perisinusoidal regions, respectively. Over the last decade, many investigative teams sought to define which cell types regulate the HSC niche, how they are organized, and to what extent they interface with each other. System dynamics requires different stromal cells to operate distinct functions over similar HSC pools rather than a single stromal cell type controlling everything. Therefore, our focus herein is to depict the players in the endosteal and subendosteal regions, named the endosteal niche, a necessary step to better understand the interactions of the HSC within the niche and to identify potential targets to manipulate and/or modulate normal and malignant HSC behavior.

Indexed as

AnimalsBone Marrow CellsHematopoietic Stem CellsHumansStem Cell NicheBONE MARROWENDOSTEUMHEMATOPOIETIC STEM CELLSIN VIVONICHEOSTEOBLAST

Identifiers

PMID25164953
PMCPMC4229422

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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.