Evidence map›Paper›PMID 26318644›Full record

ArticleJournal of autoimmunity2015

Myeloid-derived suppressor cells contribute to bone erosion in collagen-induced arthritis by differentiating to osteoclasts.

Hui Zhang, Yuefang Huang, Shuang Wang, Rong Fu, Chaohuan Guo, Hongyue Wang, Jijun Zhao, Felicia Gaskin, Jingxian Chen, Niansheng Yang and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of autoimmunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

47 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Myeloid-Derived Suppressor Cells in Inflammatory Arthritis.International journal of molecular sciences · 2026
    Review
  3. Article
  4. Review
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  6. Article
  7. Review
  8. Review
  9. Article
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  11. Tristetraprolin regulates the skeletal phenotype and osteoclastogenic potential through monocytic myeloid-derived suppressor cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. GITRL impairs the immunosuppressive function of MDSCs via PTEN-mediated signaling pathway in experimental Sjögren syndrome.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Article
  17. Article
  18. Article
  19. Review
  20. Review
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

11 authors at 3 institutions in 2 countries.

Hui ZhangDepartment of Rheumatology, First Affiliated Hospital, Sun Yat-sen University, Zhongshan Road II, 510080, Guangzhou, China.
Yuefang HuangDepartment of Pediatrics, First Affiliated Hospital, Sun Yat-sen University, Zhongshan Road II, 510080, Guangzhou, China.
Shuang WangDepartment of Rheumatology, First Affiliated Hospital, Sun Yat-sen University, Zhongshan Road II, 510080, Guangzhou, China.
Rong FuDepartment of Rheumatology, First Affiliated Hospital, Sun Yat-sen University, Zhongshan Road II, 510080, Guangzhou, China.
Chaohuan GuoDepartment of Rheumatology, First Affiliated Hospital, Sun Yat-sen University, Zhongshan Road II, 510080, Guangzhou, China.
Hongyue WangDepartment of Rheumatology, First Affiliated Hospital, Sun Yat-sen University, Zhongshan Road II, 510080, Guangzhou, China.
Jijun ZhaoDepartment of Rheumatology, First Affiliated Hospital, Sun Yat-sen University, Zhongshan Road II, 510080, Guangzhou, China.
Felicia GaskinDepartment of Psychiatry and Neurobehavioral Sciences, University of Virginia, Charlottesville, VA 22908-0203, USA.
Jingxian ChenDepartment of Pediatrics, First Affiliated Hospital, Sun Yat-sen University, Zhongshan Road II, 510080, Guangzhou, China.
Niansheng YangDepartment of Rheumatology, First Affiliated Hospital, Sun Yat-sen University, Zhongshan Road II, 510080, Guangzhou, China. Electronic address: zsuyns@163.com.
Shu Man FuDivision of Rheumatology and Center of Inflammation, Immunology and Regenerative Medicine, Department of Medicine, University of Virginia, Charlottesville, VA 22908-0133, USA; Department of Microbiology, Immunology and Cancer Biology, University of Virginia, Charlottesville, VA 22908-0133, USA.
Sun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CNUniversity of Virginia · US

Funding

Cellular and Genetic Basis of Systemic LupusR01AR047988 · NIAMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI FU, SHU MAN · 2001 to 2020
$8.4M
HLA-D Region Systemic Lupus Erythematosus PathogenesisR01AR049449 · NIAMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI FU, SHU MAN · 2005 to 2015
$4.2M
NIAMS NIH HHS R01 AR047988NIAMS NIH HHS R01-AR047988NIAMS NIH HHS R01 AR049449NIAMS NIH HHS R01-AR049449
6 · The paper itself

Abstract

Bone erosion is a sign of severe rheumatoid arthritis and osteoclasts play a major role in the bone resorption. Recently, myeloid-derived suppressor cells (MDSC) has been reported to be increased in collagen-induced arthritis (CIA). The number of circulating MDSCs is shown to correlate with rheumatoid arthritis. These findings suggest that MDSCs are precursor cells involved in bone erosion. In this study, MDSCs isolated from mice with CIA stimulated with M-CSF and RANKL in vitro expressed osteoclast markers and acquired osteoclast bone resorption function. MDSCs sorted from CIA mice were transferred into the tibia of normal DBA/1J mice and bones were subjected to histological and Micro CT analyses. The transferred CIA-MDSCs were shown to differentiate into TRAP(+) osteoclasts that were capable of bone resorption in vivo. MDSCs isolated from normal mice had more potent suppressor activity and much less capability to differentiate to osteoclast. Additional experiments showed that NF-κB inhibitor Bay 11-7082 or IκB inhibitor peptide blocked the differentiation of MDSCs to osteoclast and bone resorption. IL-1Ra also blocked this differentiation. In contrast, the addition of IL-1α further enhanced osteoclast differentiation and bone resorption. These results suggest that MDSCs are a source of osteoclast precursors and inflammatory cytokines such as IL-1, contributing significantly to erosive changes seen in rheumatoid arthritis and related disorders.

Indexed as

AnimalsArthritis, ExperimentalBone ResorptionCell DifferentiationCells, CulturedInterleukin-1alphaInterleukin 1 Receptor Antagonist ProteinMacrophage Colony-Stimulating FactorMaleMiceMice, Inbred DBAMyeloid CellsNF-kappa BNitrilesOsteoclastsRANK Ligand3-(4-methylphenylsulfonyl)-2-propenenitrileIl1rn protein, mouseInterleukin-1alphaInterleukin 1 Receptor Antagonist ProteinMacrophage Colony-Stimulating FactorNF-kappa BNitrilesRANK LigandSulfonesTnfsf11 protein, mouseBone destructionCollagen-induced arthritis and rheumatoid arthritisMDSCOsteoclastOsteoclast precursor

Identifiers

PMID26318644
PMCPMC4679657
OpenAlexW1636698109

What OpenQuestion holds

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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.