Evidence map›Paper›PMID 33567098›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2021

Sexual Dimorphism in Differentiating Osteoclast Precursors Demonstrates Enhanced Inflammatory Pathway Activation in Female Cells.

Se Hwan Mun, Sandra Jastrzebski, Judy Kalinowski, Steven Zeng, Brian Oh, Seyeon Bae, Giannopoulou Eugenia, Nazir M Khan, Hicham Drissi, Ping Zhou and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Role of Notch signaling in corticalization.Journal of endocrinological investigation · 2026
    Review
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  5. Toward Sex-Specific Biomaterials Innovation: A Perspective.ACS biomaterials science & engineering · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. Article
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  11. Review
  12. Article
  13. Germ-Free C57BL/6 Mice Have Increased Bone Mass and Altered Matrix Properties but Not Decreased Bone Fracture Resistance.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2023
    Article
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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

14 authors at 5 institutions in 1 country.

Se Hwan MunArthritis and Tissue Degeneration Program, David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, NY, USA.
Sandra JastrzebskiDepartment of Medicine, University of Connecticut Health, Farmington, CT, USA.
Judy KalinowskiDepartment of Medicine, University of Connecticut Health, Farmington, CT, USA.
Steven ZengArthritis and Tissue Degeneration Program, David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, NY, USA.
Brian OhArthritis and Tissue Degeneration Program, David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, NY, USA.
Seyeon BaeArthritis and Tissue Degeneration Program, David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, NY, USA.
Giannopoulou EugeniaArthritis and Tissue Degeneration Program, David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, NY, USA.
Nazir M KhanDepartment of Orthopaedics, School of Medicine, Emory University, Atlanta, GA, USA.
Hicham DrissiDepartment of Orthopaedics, School of Medicine, Emory University, Atlanta, GA, USA.
Ping ZhouFeil Family Brain & Mind Research Institute (BMRI), Weill Cornell Medical College, New York, NY, USA.
Bongjin ShinCenter on Aging, University of Connecticut Health, Farmington, CT, USA.
Sun-Kyeong LeeCenter on Aging, University of Connecticut Health, Farmington, CT, USA.
Joseph Lorenzo *Department of Medicine, University of Connecticut Health, Farmington, CT, USA.
Kyung-Hyun Park-Min *Arthritis and Tissue Degeneration Program, David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, NY, USA.ORCID 0000-0002-0208-6341
Hospital for Special Surgery · USUConn Health · USEmory University · USCornell University · USZero to Three · US

Funding

The Crosstalk between MYC and Metabolism during OsteoclastogenesisR01AR069562 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI PARK-MIN, KYUNG-HYUN · 2016 to 2020
$1.9M
A novel regulating pathway in osteoclastogenesis and arthritic bone resorptionR01AR073156 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI PARK-MIN, KYUNG-HYUN · 2018 to 2022
$1.9M
Runx1 Control of Bone Resorption during Fracture Repair SupplementR01AR063661 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI DRISSI, MOULAY HICHAM, LORENZO, JOSEPH A · 2013 to 2017
$1.8M
Studies of Osteoclast Lineage in Health and DiseaseR56AR074391 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LORENZO, JOSEPH A · 2019 to 2019
$412k
NIAMS NIH HHS R01 AR063661NIAMS NIH HHS R01 AR069562NIAMS NIH HHS R01 AR073156NIAMS NIH HHS R56 AR074391
6 · The paper itself

Abstract

Sexual dimorphism of the skeleton is well documented. At maturity, the male skeleton is typically larger and has a higher bone density than the female skeleton. However, the underlying mechanisms for these differences are not completely understood. In this study, we examined sexual dimorphism in the formation of osteoclasts between cells from female and male mice. We found that the number of osteoclasts in bones was greater in females. Similarly, in vitro osteoclast differentiation was accelerated in female osteoclast precursor (OCP) cells. To further characterize sex differences between female and male osteoclasts, we performed gene expression profiling of cultured, highly purified, murine bone marrow OCPs that had been treated for 3 days with macrophage colony-stimulating factor (M-CSF) and receptor activator of NF-κB ligand (RANKL). We found that 125 genes were differentially regulated in a sex-dependent manner. In addition to genes that are contained on sex chromosomes, transcriptional sexual dimorphism was found to be mediated by genes involved in innate immune and inflammatory response pathways. Furthermore, the NF-κB-NFATc1 axis was activated earlier in female differentiating OCPs, which partially explains the differences in transcriptomic sexual dimorphism in these cells. Collectively, these findings identify multigenic sex-dependent intrinsic difference in differentiating OCPs, which results from an altered response to osteoclastogenic stimulation. In humans, these differences could contribute to the lower peak bone mass and increased risk of osteoporosis that females demonstrate relative to males. © 2021 American Society for Bone and Mineral Research (ASBMR).

Indexed as

OsteoclastsSex CharacteristicsAnimalsBone Marrow CellsCell DifferentiationCells, CulturedFemaleMacrophage Colony-Stimulating FactorMaleMiceNFATC Transcription FactorsOsteogenesisRANK LigandMacrophage Colony-Stimulating FactorNFATC Transcription FactorsRANK LigandINFLAMMATORY RESPONSESOSTEOCLASTOGENESISOSTEOCLASTSSEXUAL DIMORPHISMSIGNALING PATHWAYSTRANSCRIPTOME

Identifiers

PMID33567098
PMCPMC11140852
OpenAlexW3127236158

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.