Evidence map›Paper›PMID 29278706›Full record

ArticleBiochemical and biophysical research communications2018

Endogenous acid ceramidase protects epithelial cells from Porphyromonas gingivalis-induced inflammation in vitro.

Mariane Maffei Azuma, Pooja Balani, Heike Boisvert, Mindy Gil, Kenji Egashira, Tsuguno Yamaguchi, Hatice Hasturk, Margaret Duncan, Toshihisa Kawai, Alexandru Movila

Open access · bronzeAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.3field-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

24 citing papers in PubMed, 31 citations in OpenAlex.

  1. FASEB bioAdvances · 2026
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  2. Article
  3. Article
  4. Review
  5. Sphingosine-mediated death ofInfection and immunity · 2025
    Article
  6. Journal of oral microbiology · 2025
    Article
  7. Sphingosine Prevents Rhinoviral Infections.International journal of molecular sciences · 2024
    Article
  8. Article
  9. Reduced Sphingosine in Cystic Fibrosis Increases Susceptibility toInternational journal of molecular sciences · 2023
    Article
  10. Review
  11. Article
  12. Sphingosine as a New Antifungal Agent againstInternational journal of molecular sciences · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Sphingosine kills bacteria by binding to cardiolipin.The Journal of biological chemistry · 2020
    Article
  20. Sphingosine-coating of plastic surfaces prevents ventilator-associated pneumonia.Journal of molecular medicine (Berlin, Germany) · 2019
    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

10 authors at 3 institutions in 2 countries.

Mariane Maffei AzumaThe Forsyth Institute, Cambridge, MA, USA.
Pooja BalaniThe Forsyth Institute, Cambridge, MA, USA; Harvard University School of Dental Medicine, Boston, MA, USA.
Heike BoisvertThe Forsyth Institute, Cambridge, MA, USA.
Mindy GilThe Forsyth Institute, Cambridge, MA, USA; Harvard University School of Dental Medicine, Boston, MA, USA.
Kenji EgashiraThe Forsyth Institute, Cambridge, MA, USA; Lion Corporation, Research & Development Headquarter, Odawara, Kanagawa, Japan.
Tsuguno YamaguchiThe Forsyth Institute, Cambridge, MA, USA; Lion Corporation, Research & Development Headquarter, Odawara, Kanagawa, Japan.
Hatice HasturkThe Forsyth Institute, Cambridge, MA, USA; Harvard University School of Dental Medicine, Boston, MA, USA.
Margaret DuncanThe Forsyth Institute, Cambridge, MA, USA.
Toshihisa KawaiNOVA Southeastern University, College of Dental Medicine, Fort Lauderdale, FL, USA.
Alexandru MovilaThe Forsyth Institute, Cambridge, MA, USA; Harvard University School of Dental Medicine, Boston, MA, USA; NOVA Southeastern University, College of Dental Medicine, Fort Lauderdale, FL, USA. Electronic address: amovila@nova.edu.
Harvard University · USLion Corporation (Japan) · JPNova Southeastern University · US

Funding

REGULATORY CELLS IN EXPERIMENTAL PERIODONTAL DISEASER01DE003420 · NIDCR · FORSYTH INSTITUTE · PI KAWAI, TOSHIHISA · 1985 to 2012
$4.3M
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
T-Regulatory Cells in PeriodontitisR01DE018499 · NIDCR · ADA FORSYTH INSTITUTE, INC. · PI KAWAI, TOSHIHISA · 2008 to 2011
$1.9M
Effects of aging on MIF-mediated migration of circulating osteoclast precursors to particle-induced osteolysis lesionsR03AG053615 · NIA · NOVA SOUTHEASTERN UNIVERSITY · PI MOVILA, ALEXANDRU · 2017 to 2018
$173k
REGULATORY CELLS IN EXPERIMENTAL PERIODONTAL DISEASER37DE003420 · NIDCR · FORSYTH INSTITUTE · PI TAUBMAN, MARTIN A · 1990 to 1999
–
NIA NIH HHS R03 AG053615NIDCR NIH HHS R01 DE003420NIDCR NIH HHS R01 DE018499NIDCR NIH HHS R01 DE019917NIDCR NIH HHS R37 DE003420NIDCR NIH HHS T32 DE007327
6 · The paper itself

Abstract

Ceramidases are a group of enzymes that degrade pro-inflammatory ceramide by cleaving a fatty acid to form anti-inflammatory sphingosine lipid. Thus far, acid, neutral and alkaline ceramidase isozymes have been described. However, the expression patterns of ceramidase isoforms as well as their role in periodontal disease pathogenesis remain unknown. In this study, expression patterns of ceramidase isoforms were quantified by real-time PCR and immunohistochemistry in gingival samples of patients with periodontitis and healthy subjects, as well as in EpiGingivalTM-3D culture and OBA-9 gingival epithelial cells both of which were stimulated with or without the presence of live Porphyromonas gingivalis (ATCC 33277 strain). A significantly lower level of acid ceramidase expression was detected in gingival tissues from periodontal patients compared to those from healthy subjects. In addition, acid-ceramidase expression in EpiGingival™ 3D culture and OBA-9 cells was suppressed by stimulation with P. gingivalis in vitro. No significant fluctuation was detected for neutral or alkaline ceramidases in either gingival samples or cell cultures. Next, to elucidate the role of acid ceramidase in P. gingivalis-induced inflammation in vitro, OBA-9 cells were transduced with adenoviral vector expressing the human acid ceramidase (Ad-ASAH1) gene or control adenoviral vector (Ad-control). In response to stimulation with P. gingivalis, ASAH1-over-expressing OBA-9 cells showed significantly lower mRNA expressions of caspase-3 as well as the percentage of Annexin V-positive cells, when compared with OBA-9 cells transduced with Ad-control vector. Furthermore, in response to stimulation with P. gingivalis, ASAH1-over-expressing OBA-9 cells produced less TNF-α, IL-6, and IL1β pro-inflammatory cytokines than observed in OBA-9 cells transduced with Ad-control vector. Collectively, our data show the novel discovery of anti-inflammatory and anti-apoptotic effects of acid ceramidase in host cells exposed to periodontal bacteria, and the attenuation of the expression of host-protective acid ceramidase in periodontal lesions.

Indexed as

Acid CeramidaseBacteroidaceae InfectionsEpithelial CellsFemaleHumansMaleMiddle AgedPeriodontitisPeriodontiumPorphyromonas gingivalisAcid CeramidaseAcid ceramidaseCeramidasesEpithelial cellsImmunityPeriodontal disease(s)/Periodontitis

Identifiers

PMID29278706
PMCPMC5765770
OpenAlexW2776602346

What OpenQuestion holds

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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.