Evidence map›Paper›PMID 30354669›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2019

Progenitor recruitment and adipogenic lipolysis contribute to the anabolic actions of parathyroid hormone on the skeleton.

David E Maridas, Elizabeth Rendina-Ruedy, Ron C Helderman, Victoria E DeMambro, Daniel Brooks, Anyonya R Guntur, Beate Lanske, Mary L Bouxsein, Clifford J Rosen

Open access · bronzeAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.0field-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

57 citing papers in PubMed, 72 citations in OpenAlex.

  1. Bone health in diabetes mellitus.Reviews in endocrine & metabolic disorders · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. The role of bone in whole-body energy metabolism.Nature reviews. Endocrinology · 2025
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Calorie restriction in mice impairs cortical but not trabecular peak bone mass by suppressing bone remodeling.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Nutrient uptake and metabolism in osteoblasts.Current opinion in endocrine and metabolic research · 2023
    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

9 authors at 3 institutions in 1 country.

David E MaridasMaine Medical Center Research Institute, Scarborough, Maine, USA.
Elizabeth Rendina-RuedyMaine Medical Center Research Institute, Scarborough, Maine, USA.
Ron C HeldermanMaine Medical Center Research Institute, Scarborough, Maine, USA.
Victoria E DeMambroMaine Medical Center Research Institute, Scarborough, Maine, USA.
Daniel BrooksCenter for Advanced Orthopaedic Studies, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Anyonya R GunturMaine Medical Center Research Institute, Scarborough, Maine, USA.
Beate LanskeHarvard School of Dental Medicine, Boston, Massachusetts, USA; and.
Mary L BouxseinCenter for Advanced Orthopaedic Studies, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Clifford J RosenMaine Medical Center Research Institute, Scarborough, Maine, USA.
Maine Medical Center Research Institute · USBeth Israel Deaconess Medical Center · USHarvard University · US

Funding

Understanding Factors Influencing COVID-19 Testing and Vaccination in Immigrant Low-income and Homeless Populations and Testing Targeted InterventionsU54GM115516 · NIGMS · MAINEHEALTH · PI CLIFFORD JAMES ROSEN · 2017 to 2026
$51.6M
The role of night shift work in metabolic disorders during and after pregnancyP20GM121301 · NIGMS · MAINEHEALTH · PI Qingchu Jin · 2017 to 2026
$25.1M
Interdisciplinary Study of Marrow Adiposity, Mineral Metabolism & Energy BalanceR24DK092759 · NIDDK · MAINEHEALTH · PI HOROWITZ, MARK C, MACDOUGALD, ORMOND A · 2011 to 2019
$13.0M
Progenitor Cell Analysis CoreP30GM106391 · NIGMS · MAINEHEALTH · PI WOJCHOWSKI, DON MICHAEL · 2013 to 2017
$5.7M
PTH resistance and marrow adipogenesisR01DK112374 · NIDDK · HARVARD MEDICAL SCHOOL · PI BARON, ROLAND E, ROSEN, CLIFFORD JAMES · 2017 to 2020
$2.2M
Impaired Lipophagy and Lipid Droplet Accumulation in OsteoblastsK01AR072123 · NIAMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RENDINA-RUEDY, ELIZABETH · 2017 to 2022
$549k
PTH resistance and marrow adipogenesisR56DK112374 · NIDDK · HARVARD MEDICAL SCHOOL · PI MANNSTADT, BEATE, ROSEN, CLIFFORD JAMES · 2016 to 2016
$85k
NIAMS NIH HHS K01 AR072123NIDDK NIH HHS R01 DK112374NIDDK NIH HHS R24 DK092759NIDDK NIH HHS R56 DK112374NIGMS NIH HHS P20 GM121301NIGMS NIH HHS P30 GM106391NIGMS NIH HHS U54 GM115516
6 · The paper itself

Abstract

Intermittent administration of parathyroid hormone (PTH) stimulates bone formation in vivo and also suppresses the volume of bone marrow adipose tissue (BMAT). In contrast, a calorie-restricted (CR) diet causes bone loss and induces BMAT in both mice and humans. We used the CR model to test whether PTH would reduce BMAT in mice by both altering cell fate and inducing lipolysis of marrow adipocytes. Eight-week-old mice were placed on a control (Ctrl) diet or CR diet. At 12 wk, CR and Ctrl mice were injected daily with PTH (CR/PTH or Ctrl/PTH) or vehicle for 4 wk. Two other cohorts were CR and simultaneously injected (CR + PTH or CR + Veh) for 4 wk. CR mice had low bone mass and increased BMAT in the proximal tibias. PTH significantly increased bone mass in all cohorts despite calorie restrictions. Adipocyte density and size were markedly increased with restriction of calories. PTH reduced adipocyte numbers in CR + PTH mice, whereas adipocyte size was reduced in CR/PTH-treated mice. In contrast, osteoblast number was increased 3-8-fold with PTH treatment. In vitro, bone marrow stromal cells differentiated into adipocytes and, treated with PTH, exhibited increased production of glycerol and fatty acids. Moreover, in cocultures of bone marrow adipocyte and osteoblast progenitors, PTH stimulated the transfer of fatty acids to osteoblasts. In summary, PTH administration to CR mice increased bone mass by shifting lineage allocation toward osteogenesis and inducing lipolysis of mature marrow adipocytes. The effects of PTH on bone marrow adiposity could enhance its anabolic actions by providing both more cells and more fuel for osteoblasts during bone formation.-Maridas, D. E., Rendina-Ruedy, E., Helderman, R. C., DeMambro, V. E., Brooks, D., Guntur, A. R., Lanske, B., Bouxsein, M. L., Rosen, C. J. Progenitor recruitment and adipogenic lipolysis contribute to the anabolic actions of parathyroid hormone on the skeleton.

Indexed as

AdipocytesAdipogenesisAnimalsBone ResorptionCaloric RestrictionCell DifferentiationCells, CulturedFemaleLipolysisMesenchymal Stem CellsMiceMice, Inbred C57BLOsteoblastsOsteogenesisParathyroid HormoneStem CellsParathyroid HormoneadipocytesbonefatmarrowPTH

Identifiers

PMID30354669
PMCPMC6338651
OpenAlexW2898276531

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.