Evidence map›Paper›PMID 20697725›Full record

ArticleArchives of dermatological research2010

Protease-activated receptor-2 mediates the expression of inflammatory cytokines, antimicrobial peptides, and matrix metalloproteinases in keratinocytes in response to Propionibacterium acnes.

Sang Eun Lee, Ji-Min Kim, Se Kyoo Jeong, Jeong Eun Jeon, Hyun-Ju Yoon, Min-Kyung Jeong, Seung Hun Lee

Open access · hybridAbstract read
In one paragraph

Article in Archives of dermatological research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

48 citing papers in PubMed, 110 citations in OpenAlex.

  1. Article
  2. Article
  3. An In Vitro Study of the Anti-Acne Effects ofMolecules (Basel, Switzerland) · 2025
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Genetic Variants Associated with Acne Vulgaris.International journal of general medicine · 2023
    Review
  12. A review of skin immune processes in acne.Frontiers in immunology · 2023
    Review
  13. Article
  14. Article
  15. Review
  16. The Immunogenetics of Acne.Advances in experimental medicine and biology · 2022
    Article
  17. Review
  18. Article
  19. Microorganisms · 2021
    Review
  20. Antibacterial Susceptibility Testing ofClinical, cosmetic and investigational dermatology · 2021
    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

7 authors at 3 institutions in 1 country.

Sang Eun LeeDepartment of Dermatology, Gangnam Severance Hospital, Yonsei University College of Medicine, 712 Eonjuro, Kangnam-gu, Seoul 135-720, Korea.
Ji-Min Kim
Se Kyoo Jeong
Jeong Eun Jeon
Hyun-Ju Yoon
Min-Kyung Jeong
Seung Hun Lee
Yonsei University · KRAekyung (South Korea) · KRGangnam Severance Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Propionibacterium acnes (P. acnes) has been known to produce various exogenous proteases, however, their role in acne pathogenesis remains largely unknown. Proteases elicit cellular responses, at least in part, via proteinase-activated receptor-2 (PAR-2), which is known to mediate inflammation and immune response. In this study, we investigated whether proteases from P. acnes could activate PAR-2 on keratinocytes and induce pro-inflammatory cytokines, antimicrobial peptides (AMPs), and matrix metalloproteinases (MMPs) via PAR-2 signaling. We examined PAR-2 expression and protease activity in acne lesions using immunofluorescence staining and in situ zymography. The effect of the culture supernatant of P. acnes on Ca(2+) signaling in immortalized keratinocytes (HaCaT) was measured using a fluorescence method. HaCaT cells were treated with P. acnes strain ATCC 6919 culture supernatant, with or without pretreatment with serine protease inhibitor or selective PAR-2 antagonist and the gene expression of pro-inflammatory cytokines, AMPs, and MMPs was detected using real-time reverse transcription-polymerase chain reaction. We found that the protease activity and PAR-2 expression were increased in acne lesions. The P. acnes culture supernatant induced calcium signaling in keratinocytes via PAR-2 and stimulated the mRNA expression of interleukin (IL)-1α, -8, tumor necrosis factor (TNF)-α, human beta defensin (hBD)-2, LL-37, MMP-1, -2, -3, -9, and -13 in keratinocytes, which was significantly inhibited by serine protease inhibitor as well as selective PAR-2 specific antagonist. These results indicate that PAR-2 plays an important role in the pathogenesis of acne by inducing inflammatory mediators in response to proteases secreted from P. acnes.

Indexed as

Acne VulgarisAntigens, BacterialAntimicrobial Cationic PeptidesCalcium SignalingCell Line, TransformedCytokinesGene Expression RegulationGram-Positive Bacterial InfectionsHumansInflammation MediatorsKeratinocytesMatrix MetalloproteinasesPropionibacterium acnesReceptor, PAR-2Serine Proteinase InhibitorsAntigens, BacterialAntimicrobial Cationic PeptidesCytokinesInflammation MediatorsMatrix MetalloproteinasesReceptor, PAR-2Serine Proteinase Inhibitors

Identifiers

PMID20697725
PMCPMC2970807
OpenAlexW2043804545

What OpenQuestion holds

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LicenceCC BY-NC
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.