Evidence map›Paper›PMID 23629863›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2013

Resolvin E1 regulates osteoclast fusion via DC-STAMP and NFATc1.

Min Zhu, Thomas E Van Dyke, Robert Gyurko

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-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

27 citing papers in PubMed, 57 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Is there a role for essential fatty acids in osteoporosis?European journal of clinical nutrition · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Resolvin E1's Antimicrobial Potential AgainstFrontiers in oral health · 2022
    Article
  11. Resolvin D1 shows osseous-protectionFrontiers in immunology · 2022
    Article
  12. Review
  13. Article
  14. Review
  15. The pathophysiology of immunoporosis: innovative therapeutic targets.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
    Review
  16. Review
  17. Article
  18. Article
  19. Chemokine-like receptor 1 deficiency leads to lower bone mass in male mice.Cellular and molecular life sciences : CMLS · 2019
    Article
  20. OC-STAMP promotes osteoclast fusion for pathogenic bone resorption in periodontitis via up-regulation of permissive fusogen CD9.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    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 2 institutions in 2 countries.

Min ZhuDepartment of Periodontology and Oral Biology, Goldman School of Dental Medicine, Boston University, Boston, Massachusetts 02118, USA.
Thomas E Van Dyke
Robert Gyurko
Boston University · USBritish Society of Periodontology · GB

Funding

Novel Mechanisms in Resolution to Harness Inflammation for ReconstructionR01DE019938 · NIDCR · BRIGHAM AND WOMEN'S HOSPITAL · PI IRIMIA, DANIEL, SERHAN, CHARLES NICHOLAS · 2009 to 2012
$2.7M
NIDCR NIH HHS DE19938NIDCR NIH HHS R01 DE019938
6 · The paper itself

Abstract

Interactions between the immune and skeletal systems in inflammatory bone diseases are well appreciated, but the underlying molecular mechanisms that coordinate the resolution phase of inflammation and bone turnover have not been unveiled. Here we investigated the direct actions of the proresolution mediator resolvin E1 (RvE1) on bone-marrow-cell-derived osteoclasts in an in vitro murine model of osteoclast maturation and inflammatory bone resorption. Investigation of the actions of RvE1 treatment on the specific stages of osteoclast maturation revealed that RvE1 targeted late stages of osteoclast maturation to decrease osteoclast formation by 32.8%. Time-lapse vital microscopy and migration assays confirmed that membrane fusion of osteoclast precursors was inhibited. The osteoclast fusion protein DC-STAMP was specifically targeted by RvE1 receptor binding and was down-regulated by 65.4%. RvE1 did not affect the induction of the essential osteoclast transcription factor nuclear factor of activated T cells c1 (NFATc1) or its nuclear translocation; however, NFATc1 binding to the DC-STAMP promoter was significantly inhibited by 60.9% with RvE1 treatment as shown in electrophoresis mobility shift assay. Our findings suggest that proresolution mediators act directly on osteoclasts, in addition to down-regulation of inflammation, providing a novel mechanism for modulating osteoclast signaling in osteolytic inflammatory disease.

Indexed as

AnimalsBlotting, WesternCell DifferentiationCell FusionCells, CulturedEicosapentaenoic AcidMembrane ProteinsMiceMice, Inbred C57BLMicroscopy, ConfocalNerve Tissue ProteinsNFATC Transcription FactorsOsteoclastsPromoter Regions, GeneticProtein BindingRANK Ligand5S,12R,18R-trihydroxy-6Z,8E,10E,14Z,16E-eicosapentaenoic acidDC-STAMP protein, mouseEicosapentaenoic AcidLtb4r1 protein, mouseMembrane ProteinsNerve Tissue ProteinsNfatc1 protein, mouseNFATC Transcription FactorsRANK LigandReceptors, Leukotriene B4Tnfsf11 protein, mouseinflammation resolutionlipid mediatorosteoimmunology

Identifiers

PMID23629863
PMCPMC3714580
OpenAlexW2120449014

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.