Evidence map›Paper›PMID 36614313›Full record

ArticleInternational journal of molecular sciences2023

The Antimicrobial Peptide Cathelicidin Exerts Immunomodulatory Effects via Scavenger Receptors.

Ryo Amagai, Toshiya Takahashi, Hitoshi Terui, Taku Fujimura, Kenshi Yamasaki, Setsuya Aiba, Yoshihide Asano

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Cecropin anisaxin-2S hasFrontiers in immunology · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Nutrients · 2024
    Article
  14. Review
  15. Review
  16. Shedding Light on Skin Autoimmunity: More than Just Skin Deep.International journal of molecular sciences · 2023
    Article
  17. Review
  18. 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 1 institution in 1 country.

Ryo AmagaiDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.
Toshiya TakahashiDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.ORCID 0000-0001-9742-2282
Hitoshi TeruiDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.ORCID 0000-0002-7598-2833
Taku FujimuraDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.
Kenshi YamasakiDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.ORCID 0000-0002-5495-4956
Setsuya AibaDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.
Yoshihide AsanoDepartment of Dermatology, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.ORCID 0000-0001-5560-9778
Tohoku University · JP

Funding

GlaxoSmithKline Japan Research Grant 2019Japan Society for the Promotion of Science 18H06136Japan Society for the Promotion of Science 19K21251Japan Society for the Promotion of Science 20K17304
6 · The paper itself

Abstract

An active form of cathelicidin antimicrobial peptide, LL-37, has immunomodulatory and stimulatory effects, though the specific pathways are not clear. The purpose of this study was to identify the cellular pathways by which LL-37 amplifies the inflammation induced by damage-associated molecular patterns (DAMPs). We performed DNA microarray, reverse transcription polymerase chain reaction, immunoblotting, and proximity ligation assays using cultured keratinocytes treated with LL-37 and/or the DAMP poly(I:C), a synthetic double-stranded RNA. In contrast to the combination of LL-37 and poly(I:C), LL-37 alone induced genes related to biological metabolic processes such as VEGFA and PTGS2 (COX-2). Inhibition of FPR2, a known receptor for cathelicidin, partially suppressed the induction of VEGFA and PTGS2. Importantly, VEGFA and PTGS2 induced by LL-37 alone were diminished by the knockdown of scavenger receptors including SCARB1 (SR-B1), OLR1 (SR-E1), and AGER (SR-J1). Moreover, LL-37 alone, as well as the combination of LL-37 and poly(I:C), showed proximity to the scavenger receptors, indicating that LL-37 acts via scavenger receptors and intermediates between them and poly(I:C). These results showed that the broad function of cathelicidin is generally dependent on scavenger receptors. Therefore, inhibitors of scavenger receptors or non-functional mock cathelicidin peptides may serve as new anti-inflammatory and immunosuppressive agents.

Indexed as

CathelicidinsImmunomodulationReceptors, ScavengerCyclooxygenase 2HumansPoly I-CCAMP protein, humanCathelicidinsCyclooxygenase 2Poly I-CReceptors, Scavengercathelicidindamage-associated molecular patterns (DAMPs)innate immunitypsoriasisscavenger receptors

Identifiers

PMID36614313
PMCPMC9821026
OpenAlexW4313585010

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.