Evidence map›Paper›PMID 34255809›Full record

ArticlePLoS pathogens2021

Treponema denticola dentilisin triggered TLR2/MyD88 activation upregulates a tissue destructive program involving MMPs via Sp1 in human oral cells.

Sean Ganther, Allan Radaic, Erin Malone, Pachiyappan Kamarajan, Nai-Yuan Nicholas Chang, Christian Tafolla, Ling Zhan, J Christopher Fenno, Yvonne L Kapila

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 31 citations in OpenAlex.

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  16. The Emerging Role of MMP12 in the Oral Environment.International journal of molecular sciences · 2023
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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

9 authors at 2 institutions in 1 country.

Sean GantherDepartment of Orofacial Sciences, School of Dentistry, University of California San Francisco, San Francisco, California, United States of America.ORCID 0000-0001-7553-155X
Allan RadaicDepartment of Orofacial Sciences, School of Dentistry, University of California San Francisco, San Francisco, California, United States of America.ORCID 0000-0002-0899-9061
Erin MaloneDepartment of Orofacial Sciences, School of Dentistry, University of California San Francisco, San Francisco, California, United States of America.ORCID 0000-0001-8356-7413
Pachiyappan KamarajanDepartment of Orofacial Sciences, School of Dentistry, University of California San Francisco, San Francisco, California, United States of America.
Nai-Yuan Nicholas ChangDepartment of Orofacial Sciences, School of Dentistry, University of California San Francisco, San Francisco, California, United States of America.
Christian TafollaDepartment of Orofacial Sciences, School of Dentistry, University of California San Francisco, San Francisco, California, United States of America.
Ling ZhanDepartment of Orofacial Sciences, School of Dentistry, University of California San Francisco, San Francisco, California, United States of America.
J Christopher FennoDepartment of Biological and Material Sciences & Prosthodontics, School of Dentistry, University of Michigan, Ann Arbor, Michigan, United States of America.ORCID 0000-0002-7073-7855
Yvonne L KapilaDepartment of Orofacial Sciences, School of Dentistry, University of California San Francisco, San Francisco, California, United States of America.ORCID 0000-0003-1330-0654
University of California, San Francisco · USUniversity of Michigan · US

Funding

UCSF INTEGRATED DDS-PHD TRAINING PROGRAMT32DE007306 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Yukiko Nakano · 1996 to 2026
$15.4M
Treponema - Host Cell and Tissue InteractionsR01DE025225 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI J CHRISTOPHER FENNO, Yvonne L Kapila · 2015 to 2026
$6.3M
Characterization of Treponema Denticola-Mediated Interactions With Periodontal Ligament Cells Leading to Persistent Host Cell/Tissue DestructionF30DE027598 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MALONE, ERIN TRENT · 2017 to 2022
$280k
NIDCR NIH HHS F30 DE027598NIDCR NIH HHS R01 DE025225NIDCR NIH HHS T32 DE007306
6 · The paper itself

Abstract

Periodontal disease is driven by dysbiosis in the oral microbiome, resulting in over-representation of species that induce the release of pro-inflammatory cytokines, chemokines, and tissue-remodeling matrix metalloproteinases (MMPs) in the periodontium. These chronic tissue-destructive inflammatory responses result in gradual loss of tooth-supporting alveolar bone. The oral spirochete Treponema denticola, is consistently found at significantly elevated levels in periodontal lesions. Host-expressed Toll-Like Receptor 2 (TLR2) senses a variety of bacterial ligands, including acylated lipopolysaccharides and lipoproteins. T. denticola dentilisin, a surface-expressed protease complex comprised of three lipoproteins has been implicated as a virulence factor in periodontal disease, primarily due to its proteolytic activity. While the role of acylated bacterial components in induction of inflammation is well-studied, little attention has been given to the potential role of the acylated nature of dentilisin. The purpose of this study was to test the hypothesis that T. denticola dentilisin activates a TLR2-dependent mechanism, leading to upregulation of tissue-destructive genes in periodontal tissue. RNA-sequencing of periodontal ligament cells challenged with T. denticola bacteria revealed significant upregulation of genes associated with extracellular matrix organization and degradation including potentially tissue-specific inducible MMPs that may play novel roles in modulating host immune responses that have yet to be characterized within the context of oral disease. The Gram-negative oral commensal, Veillonella parvula, failed to upregulate these same MMPs. Dentilisin-induced upregulation of MMPs was mediated via TLR2 and MyD88 activation, since knockdown of expression of either abrogated these effects. Challenge with purified dentilisin upregulated the same MMPs while a dentilisin-deficient T. denticola mutant had no effect. Finally, T. denticola-mediated activation of TLR2/MyD88 lead to the nuclear translocation of the transcription factor Sp1, which was shown to be a critical regulator of all T. denticola-dependent MMP expression. Taken together, these data suggest that T. denticola dentilisin stimulates tissue-destructive cellular processes in a TLR2/MyD88/Sp1-dependent fashion.

Indexed as

Periodontal DiseasesBacterial ProteinsCells, CulturedHumansMatrix MetalloproteinasesMyeloid Differentiation Factor 88Peptide HydrolasesPeriodontal LigamentSp1 Transcription FactorToll-Like Receptor 2Treponema denticolaTreponemal InfectionsUp-RegulationVirulence FactorsBacterial ProteinsdentilisinMatrix MetalloproteinasesMYD88 protein, humanMyeloid Differentiation Factor 88Peptide HydrolasesSP1 protein, humanSp1 Transcription FactorTLR2 protein, humanToll-Like Receptor 2Virulence Factors

Identifiers

PMID34255809
PMCPMC8301614
OpenAlexW3178906930

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.