<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dernovics A</submitter><funding>European Regional Development Fund</funding><pagination>3018</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10669503</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(11)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Phenol-soluble modulins (PSMs) are pore-forming toxins (PFTs) produced by staphylococci. PSMs exert diverse cellular effects, including lytic, pro-apoptotic, pro-inflammatory and antimicrobial actions. Since the effects of PSMs on autophagy have not yet been reported, we evaluated the autophagic activity in HaCaT keratinocytes treated with recombinant PSMα3.&lt;h4>Methods&lt;/h4>The autophagic flux and levels of autophagic marker proteins were determined using Western blot analysis. Subcellular localization of LC3B and Beclin-1 was investigated using an indirect immunofluorescence assay. The ultrastructural features of control and PSMα3-treated cells were evaluated via transmission electron microscopy. Cytoplasmic acidification was measured via acridine orange staining. Phosph</pubmed_abstract><journal>Biomedicines</journal><pubmed_title>Phenol-Soluble Modulin α3 Stimulates Autophagy in HaCaT Keratinocytes.</pubmed_title><pmcid>PMC10669503</pmcid><funding_grant_id>EFOP-3.6.1-16-2016-00008</funding_grant_id><pubmed_authors>Megyeri K</pubmed_authors><pubmed_authors>Razga Z</pubmed_authors><pubmed_authors>Ayaydin F</pubmed_authors><pubmed_authors>Seprenyi G</pubmed_authors><pubmed_authors>Vereb Z</pubmed_authors><pubmed_authors>Dernovics A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phenol-Soluble Modulin α3 Stimulates Autophagy in HaCaT Keratinocytes.</name><description>&lt;h4>Background&lt;/h4>Phenol-soluble modulins (PSMs) are pore-forming toxins (PFTs) produced by staphylococci. PSMs exert diverse cellular effects, including lytic, pro-apoptotic, pro-inflammatory and antimicrobial actions. Since the effects of PSMs on autophagy have not yet been reported, we evaluated the autophagic activity in HaCaT keratinocytes treated with recombinant PSMα3.&lt;h4>Methods&lt;/h4>The autophagic flux and levels of autophagic marker proteins were determined using Western blot analysis. Subcellular localization of LC3B and Beclin-1 was investigated using an indirect immunofluorescence assay. The ultrastructural features of control and PSMα3-treated cells were evaluated via transmission electron microscopy. Cytoplasmic acidification was measured via acridine orange staining. Phosph</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2025-04-19T13:50:48.798Z</modification><creation>2025-04-19T13:50:48.798Z</creation></dates><accession>S-EPMC10669503</accession><cross_references><pubmed>38002017</pubmed><doi>10.3390/biomedicines11113018</doi></cross_references></HashMap>