<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Amagai R</submitter><funding>GlaxoSmithKline Japan</funding><funding>Japan Society for the Promotion of Science</funding><pagination>875</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9821026</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_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</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>The Antimicrobial Peptide Cathelicidin Exerts Immunomodulatory Effects via Scavenger Receptors.</pubmed_title><pmcid>PMC9821026</pmcid><funding_grant_id>19K21251</funding_grant_id><funding_grant_id>20K17304</funding_grant_id><funding_grant_id>Research Grant 2019</funding_grant_id><funding_grant_id>18H06136</funding_grant_id><pubmed_authors>Takahashi T</pubmed_authors><pubmed_authors>Fujimura T</pubmed_authors><pubmed_authors>Asano Y</pubmed_authors><pubmed_authors>Yamasaki K</pubmed_authors><pubmed_authors>Aiba S</pubmed_authors><pubmed_authors>Amagai R</pubmed_authors><pubmed_authors>Terui H</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Antimicrobial Peptide Cathelicidin Exerts Immunomodulatory Effects via Scavenger Receptors.</name><description>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</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-21T16:18:08.1Z</modification><creation>2025-04-21T16:18:08.1Z</creation></dates><accession>S-EPMC9821026</accession><cross_references><pubmed>36614313</pubmed><doi>10.3390/ijms24010875</doi></cross_references></HashMap>