Evidence map›Paper›PMID 29492879›Full record

ReviewCurrent osteoporosis reports2018

Metabolic Coupling Between Bone Marrow Adipose Tissue and Hematopoiesis.

Russell T Turner, Stephen A Martin, Urszula T Iwaniec

Abstract readReview
In one paragraph

Review in Current osteoporosis reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
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  9. Article
  10. Review
  11. Article
  12. Article
  13. Sclerostin Depletion Induces Inflammation in the Bone Marrow of Mice.International journal of molecular sciences · 2021
    Article
  14. Article
  15. Review
  16. Observational
  17. Article
  18. The Effects of Sclerostin on the Immune System.Current osteoporosis reports · 2020
    Review
  19. Article
  20. 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 at 1 institution in 1 country.

Russell T TurnerSkeletal Biology Laboratory, School of Biological and Population Health Sciences, Oregon State University, Corvallis, OR, 97331, USA.
Stephen A MartinSkeletal Biology Laboratory, School of Biological and Population Health Sciences, Oregon State University, Corvallis, OR, 97331, USA.
Urszula T IwaniecSkeletal Biology Laboratory, School of Biological and Population Health Sciences, Oregon State University, Corvallis, OR, 97331, USA. urszula.iwaniec@oregonstate.edu.
Oregon State University · US

Funding

The Role of Leptin in Inflammation-Driven Bone LossR01AR060913 · NIAMS · OREGON STATE UNIVERSITY · PI IWANIEC, URSZULA T · 2011 to 2025
$3.5M
Mast Cells Mediate the Skeletal Response to Intermittent and Continuous PTHR21AR066811 · NIAMS · OREGON STATE UNIVERSITY · PI TURNER, RUSSELL THOMAS · 2015 to 2016
$355k
NIAMS NIH HHS R01 AR060913NIAMS NIH HHS R21 AR066811
6 · The paper itself

Abstract

purpose of reviewMesenchymal stem cells (MSCs) located in the bone marrow have the capacity to differentiate into multiple cell lineages, including osteoblast and adipocyte. Adipocyte density within marrow is inversely associated with bone mass during aging and in some pathological conditions, contributing to the prevailing view that marrow adipocytes play a largely negative role in bone metabolism. However, a negative association between marrow adipocytes and bone balance is not universal. Although MAT levels appear tightly regulated, establishing the precise physiological significance of MAT has proven elusive. Here, we review recent literature aimed at delineating the function of MAT. RECENT

findingsAn important physiological function of MAT may be to provide an expandable/contractible fat depot, which is critical for minimization of energy requirements for sustaining optimal hematopoiesis. Because the energy requirements for storing fat are negligible compared to those required to maintain hematopoiesis, even small reductions in hematopoietic tissue volume to match a reduced requirement for hematopoiesis could represent an important reduction in energy cost. Such a physiological function would require tight coupling between hematopoietic stem cells and MSCs to regulate the balance between MAT and hematopoiesis. Kit-ligand, an important regulator of proliferation, differentiation, and survival of hematopoietic cells, may function as a prototypic factor coupling MAT and hematopoiesis. Crosstalk between hematopoietic and mesenchymal cells in the bone marrow may contribute to establishing the balance between MAT levels and hematopoiesis.

Indexed as

AdipocytesAdipose TissueAgingBone MarrowBone RemodelingCell DifferentiationCell ProliferationCell SurvivalHematopoiesisHematopoietic Stem CellsHumansMesenchymal Stem CellsOsteoblastsStem Cell FactorStem Cell FactorAdipocyteBone remodelingHematopoiesisKit-ligandOsteoblast

Identifiers

PMID29492879
PMCPMC5989569
OpenAlexW2790377769

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.