Evidence map›Paper›PMID 28199142›Full record

ArticleJournal of dental research2017

DC-STAMP Is an Osteoclast Fusogen Engaged in Periodontal Bone Resorption.

W Wisitrasameewong, M Kajiya, A Movila, S Rittling, T Ishii, M Suzuki, S Matsuda, Y Mazda, M R Torruella, M M Azuma and 7 more

Open access · greenAbstract read
In one paragraph

Article in Journal of dental research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

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  17. 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
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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

17 authors at 6 institutions in 3 countries.

W Wisitrasameewong1 Department of Periodontology, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.
M Kajiya4 Hiroshima University Graduate School of Biomedical Sciences, Periodontal Medicine, Hiroshima, Japan.
A Movila2 Department of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, MA, USA.
S Rittling2 Department of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, MA, USA.
T Ishii5 Tokyo Dental College, Tokyo, Chiyoda-ku, Japan.
M Suzuki6 College of Dentistry, The Ohio State University, Columbus, OH, USA.
S Matsuda4 Hiroshima University Graduate School of Biomedical Sciences, Periodontal Medicine, Hiroshima, Japan.
Y Mazda2 Department of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, MA, USA.
M R Torruella2 Department of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, MA, USA.
M M Azuma2 Department of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, MA, USA.
K Egashira2 Department of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, MA, USA.
M O Freire2 Department of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, MA, USA.
H Sasaki2 Department of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, MA, USA.
C Y Wang9 UCLA, Lab of Molecular Signaling, Division of Oral Biology and Medicine, UCLA, Los Angeles, CA, USA.
X Han2 Department of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, MA, USA.
M A Taubman2 Department of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, MA, USA.
T Kawai10 Department of Periodontology, NOVA Southeastern University College of Dental Medicine, Fort Lauderdale, FL, USA.
Hiroshima University · JPChulalongkorn University · THLion Corporation (Japan) · JPNova Southeastern University · USThe Ohio State University · USTokyo Dental College · JP

Funding

Regulatory B Cells in the Amelioration of Immune-Mediated Periodontal DiseaseR01DE025255 · NIDCR · NOVA SOUTHEASTERN UNIVERSITY · PI HAN, XIAOZHE · 2015 to 2025
$5.8M
FORSYTH POSTDOCTORAL TRAINING IN ORAL HEALTH RESEARCHT32DE007327 · NIDCR · FORSYTH INSTITUTE · PI VAN DYKE, THOMAS ELLIOTT · 2001 to 2015
$3.5M
Programming dendritic cells in concert with morphagen delivery for periodontal reR01DE019917 · NIDCR · HARVARD UNIVERSITY · PI KAWAI, TOSHIHISA, MOONEY, DAVID J · 2009 to 2013
$3.5M
Osteopontin and Integrins in Innate Immune Responses to Polymicrobial InfectionR01DE022380 · NIDCR · ADA FORSYTH INSTITUTE, INC. · PI RITTLING, SUSAN R · 2012 to 2016
$2.4M
T-Regulatory Cells in PeriodontitisR01DE018499 · NIDCR · ADA FORSYTH INSTITUTE, INC. · PI KAWAI, TOSHIHISA · 2008 to 2011
$1.9M
Regulation of ChemR23 in Resolution of InflammationR00DE023584 · NIDCR · J. CRAIG VENTER INSTITUTE, INC. · PI FREIRE, MARCELO · 2015 to 2019
$1.2M
NIDCR NIH HHS R01 DE018499NIDCR NIH HHS R01 DE019917NIDCR NIH HHS R01 DE022380NIDCR NIH HHS R01 DE025255NIDCR NIH HHS T32 DE007327
6 · The paper itself

Abstract

Dendritic cell-specific transmembrane protein (DC-STAMP) plays a key role in the induction of osteoclast (OC) cell fusion, as well as DC-mediated immune regulation. While DC-STAMP gene expression is upregulated in the gingival tissue with periodontitis, its pathophysiological roles in periodontitis remain unclear. To evaluate the effects of DC-STAMP in periodontitis, anti-DC-STAMP-monoclonal antibody (mAb) was tested in a mouse model of ligature-induced periodontitis ( n = 6-7/group) where Pasteurella pneumotropica ( Pp)-reactive immune response activated T cells to produce receptor activator of nuclear factor kappa-B ligand (RANKL), which, in turn, promotes the periodontal bone loss via upregulation of osteoclastogenesis. DC-STAMP was expressed on the cell surface of mature multinuclear OCs, as well as immature mononuclear OCs, in primary cultures of RANKL-stimulated bone marrow cells. Anti-DC-STAMP-mAb suppressed the emergence of large, but not small, multinuclear OCs, suggesting that DC-STAMP is engaged in the late stage of cell fusion. Anti-DC-STAMP-mAb also inhibited pit formation caused by RANKL-stimulated bone marrow cells. Attachment of ligature to a second maxillary molar induced DC-STAMP messenger RNA and protein, along with elevated tartrate-resistant acid phosphatase-positive (TRAP+) OCs and alveolar bone loss. As we expected, systemic administration of anti-DC-STAMP-mAb downregulated the ligature-induced alveolar bone loss. Importantly, local injection of anti-DC-STAMP-mAb also suppressed alveolar bone loss and reduced the total number of multinucleated TRAP+ cells in mice that received ligature attachment. Attachment of ligature induced significantly elevated tumor necrosis factor-α, interleukin-1β, and RANKL in the gingival tissue compared with the control site without ligature ( P < 0.05), which was unaffected by local injection with either anti-DC-STAMP-mAb or control-mAb. Neither in vivo anti- Pp IgG antibody nor in vitro anti- Pp T-cell response and resultant production of RANKL was affected by anti-DC-STAMP-mAb. This study illustrated the roles of DC-STAMP in promoting local OC cell fusion without affecting adaptive immune responses to oral bacteria. Therefore, it is plausible that a novel therapeutic regimen targeting DC-STAMP could suppress periodontal bone loss.

Indexed as

AnimalsAntibodies, MonoclonalBlotting, WesternBone ResorptionCell DifferentiationCell FusionDisease Models, AnimalEnzyme-Linked Immunosorbent AssayGene Expression RegulationMaleMembrane ProteinsMiceMice, Inbred C57BLNerve Tissue ProteinsOsteoclastsPeriodontitisAntibodies, MonoclonalDC-STAMP protein, mouseMembrane ProteinsNerve Tissue ProteinsRANK Ligandbone resorptioncell fusionimmunitymiceosteoclastsperiodontal disease(s)/periodontitis

Identifiers

PMID28199142
PMCPMC5444615
OpenAlexW2588535141

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.