Evidence map›Paper›PMID 35039202›Full record

ArticleAmerican journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics2022

Orthodontic loading activates cell-specific autophagy in a force-dependent manner.

Laura Anne Jacox, Na Tang, Yina Li, Clare Bocklage, Christina Graves, Shannon Coats, Michael Miao, Tim Glesener, Jane Kwon, Natalie Giduz and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

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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

13 authors at 5 institutions in 2 countries.

Laura Anne JacoxDivision of Craniofacial and Surgical Care, and Division of Oral and Craniofacial Health Sciences, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC.
Na TangDivision of Oral and Craniofacial Health Sciences, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC Department of Oral Medicine, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu, Sichuan, China.
Yina LiDivision of Craniofacial and Surgical Care, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC.
Clare BocklageDivision of Craniofacial and Surgical Care, and Division of Oral and Craniofacial Health Sciences, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC.
Christina GravesDivision of Oral and Craniofacial Health Sciences, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC.
Shannon CoatsDuke University School of Medicine, Durham, NC.
Michael MiaoCurriculum in Oral and Craniofacial Biomedicine, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC.
Tim GlesenerDivision of Oral and Craniofacial Health Sciences, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC.
Jane KwonDivision of Craniofacial and Surgical Care, and Division of Oral and Craniofacial Health Sciences, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC.
Natalie GiduzDivision of Craniofacial and Surgical Care, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC.
Feng-Chang LinDepartment of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC.
Jennifer MartinezNational Institutes of Health, Bethesda, Md National Institute of Environmental Health Sciences, Research Triangle Park, Durham, NC.
Ching-Chang KoDivision of Orthodontics, College of Dentistry, The Ohio State University, Columbus, Ohio. Electronic address: Ko.367@osu.edu.
University of North Carolina at Chapel Hill · USDuke University · USNational Institutes of Health · USSichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital · CNThe Ohio State University · US

Funding

Engineering novel bio-inspired materials for stem-cell mediated bone regenerationR01DE022816 · NIDCR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KO, CHING-CHANG · 2014 to 2018
$2.0M
NIDCR NIH HHS R01 DE022816
6 · The paper itself

Abstract

introductionOrthodontic tooth movement (OTM) relies on bone remodeling and controlled aseptic inflammation. Autophagy, a conserved homeostatic pathway, has been shown to play a role in bone turnover. We hypothesize that autophagy participates in regulating bone remodeling during OTM in a force-dependent and cell type-specific manner.

methodsA split-mouth design was used to load molars with 1 of 3 force levels (15, 30, or 45 g of force) in mice carrying a green fluorescent protein-LC3 transgene to detect cellular autophagy. Fluorescent microscopy and quantitative polymerase chain reaction analyses were used to evaluate autophagy activation and its correlation with force level. Cell type-specific antibodies were used to identify cells with green fluorescent protein-positive puncta (autophagosomes) in periodontal tissues.

resultsAutophagic activity increased shortly after loading with moderate force and was associated with the expression of bone turnover, inflammatory, and autophagy markers. Different load levels resulted in altered degrees of autophagic activation, gene expression, and osteoclast recruitment. Autophagy was specifically induced by loading in macrophages and osteoclasts found in the periodontal ligament and alveolar bone. Data suggest autophagy participates in regulating bone turnover during OTM.

conclusionsAutophagy is induced in macrophage lineage cells by orthodontic loading in a force-dependent manner and plays a role during OTM, possibly through modulation of osteoclast bone resorption. Exploring the roles of autophagy in OTM is medically relevant, given that autophagy is associated with oral and systemic inflammatory conditions.

Indexed as

OsteoclastsTooth Movement TechniquesAnimalsAutophagyBone RemodelingMicePeriodontal Ligament

Identifiers

PMID35039202
PMCPMC10971665
OpenAlexW4205208082

What OpenQuestion holds

Textmetadata
LicenceTDM
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.