Evidence map›Paper›PMID 27514746›Full record

ArticleThe Journal of biological chemistry2016

Plasticity of Myeloid Cells during Oral Barrier Wound Healing and the Development of Bisphosphonate-related Osteonecrosis of the Jaw.

Yujie Sun, Kawaljit Kaur, Keiichi Kanayama, Kenzo Morinaga, Sil Park, Akishige Hokugo, Anna Kozlowska, William H McBride, Jun Li, Anahid Jewett and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

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  11. Surgical Treatment of Medication-Related Osteonecrosis of the Jaw: A Retrospective Study.International journal of environmental research and public health · 2020
    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

11 authors at 5 institutions in 4 countries.

Yujie SunFrom the Department of Dental Implant Centre, Beijing Stomatological Hospital, School of Stomatology, Capital Medical University, Beijing 100050, China, Weintraub Center for Reconstructive Biotechnology, Division of Advanced Prosthodontics, and.
Kawaljit KaurWeintraub Center for Reconstructive Biotechnology, Division of Oral Medicine and Biology, UCLA School of Dentistry, Los Angeles, California 90095.
Keiichi KanayamaWeintraub Center for Reconstructive Biotechnology, Department of Periodontology, Asahi University School of Dentistry, Gifu, Japan 501-0296.
Kenzo MorinagaWeintraub Center for Reconstructive Biotechnology, Department of Oral Rehabilitation, Fukuoka Dental College, Fukuoka, Japan 814-0175.
Sil ParkWeintraub Center for Reconstructive Biotechnology, Division of Advanced Prosthodontics, and Division of Oral Medicine and Biology, UCLA School of Dentistry, Los Angeles, California 90095.
Akishige HokugoWeintraub Center for Reconstructive Biotechnology, Division of Plastic and Reconstructive Surgery, David Geffen School of Medicine at UCLA, Los Angeles, California 90095.
Anna KozlowskaWeintraub Center for Reconstructive Biotechnology, Division of Oral Medicine and Biology, UCLA School of Dentistry, Los Angeles, California 90095, Department of Tumor Immunology, Chair of Medical Biotechnology, Poznan University of Medical Sciences, Poznan, Poland 61-866, and.
William H McBrideDivision of Molecular and Cellular Oncology, David Geffen School of Medicine at UCLA, Los Angeles, California 90095.
Jun LiFrom the Department of Dental Implant Centre, Beijing Stomatological Hospital, School of Stomatology, Capital Medical University, Beijing 100050, China, lijun3021@aliyun.com.
Anahid JewettWeintraub Center for Reconstructive Biotechnology, Division of Oral Medicine and Biology, UCLA School of Dentistry, Los Angeles, California 90095, ajewett@dentistry.ucla.edu.
Ichiro NishimuraWeintraub Center for Reconstructive Biotechnology, Division of Advanced Prosthodontics, and Division of Oral Medicine and Biology, UCLA School of Dentistry, Los Angeles, California 90095, inishimura@dentistry.ucla.edu.
University of California, Los Angeles · USCapital Medical University · CNAsahi University · JPFukuoka Dental College · JPPoznan University of Medical Sciences · PL

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
UCLA Center for Biological RadioprotectorsU19AI067769 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MCBRIDE, WILLIAM H. · 2005 to 2019
$44.6M
Oral Mucosa Barrier and Bisphosphonate-related Osteonecrosis of the JawR01DE022552 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI NISHIMURA, ICHIRO · 2012 to 2016
$2.2M
Molecular and cellular mechanism of ONJ related to osteoclast inhibitionR21DE023410 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MCKENNA, CHARLES E, NISHIMURA, ICHIRO · 2014 to 2015
$451k
EXTRAMURAL RESEARCH FACILITIES CONSTRUCTION PROJECTSC06RR014529 · NCRR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PARK, NO-HEE · 1999 to 1999
–
NCI NIH HHS P30 CA016042NCRR NIH HHS C06 RR014529NIAID NIH HHS U19 AI067769NIDCR NIH HHS R01 DE022552NIDCR NIH HHS R21 DE023410
6 · The paper itself

Abstract

Injury to the barrier tissue initiates a rapid distribution of myeloid immune cells from bone marrow, which guide sound wound healing. Bisphosphonates, a widely used anti-bone resorptive drug with minimal systemic side effects, have been linked to an abnormal wound healing in the oral barrier tissue leading to, in some cases, osteonecrosis of the jaw (ONJ). Here we report that the development of ONJ may involve abnormal phenotypic plasticity of Ly6G+/Gr1+ myeloid cells in the oral barrier tissue undergoing tooth extraction wound healing. A bolus intravenous zoledronate (ZOL) injection to female C57Bl/6 mice followed by maxillary first molar extraction resulted in the development of ONJ-like lesion during the second week of wound healing. The multiplex assay of dissociated oral barrier cells exhibited the secretion of cytokines and chemokines, which was significantly modulated in ZOL mice. Tooth extraction-induced distribution of Ly6G+/Gr1+ cells in the oral barrier tissue increased in ZOL mice at week 2. ONJ-like lesion in ZOL mice contained Ly6G+/Gr1+ cells with abnormal size and morphology as well as different flow cytometric staining intensity. When anti-Ly6G (Gr1) antibody was intraperitoneally injected for 5 days during the second week of tooth extraction, CD11b+GR1(hi) cells in bone marrow and Ly6G+ cells in the oral barrier tissue were depleted, and the development of ONJ-like lesion was significantly attenuated. This study suggests that local modulation of myeloid cell plasticity in the oral barrier tissue may provide the basis for pathogenesis and thus therapeutic as well as preventive strategy of ONJ.

Indexed as

AnimalsAntigens, LyBisphosphonate-Associated Osteonecrosis of the JawBone MarrowFemaleMiceMouthMyeloid CellsTooth ExtractionWound HealingAntigens, LyLy6G antigen, mousebonebone marrownecrosis (necrotic death)neutrophilwound healing

Identifiers

PMID27514746
PMCPMC5034053
OpenAlexW2509370936

What OpenQuestion holds

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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.