Matches in SemOpenAlex for { <https://semopenalex.org/work/W2893863934> ?p ?o ?g. }
- W2893863934 endingPage "12" @default.
- W2893863934 startingPage "1" @default.
- W2893863934 abstract "In its classical genomic mode of action, the aryl hydrocarbon receptor (AhR) acts as a ligand activated transcription factor regulating expression of target genes such as CYP1A1 and CYP1B1. Some ligands may also trigger more rapid nongenomic responses through AhR, including calcium signaling (Ca2+). In the present study we observed that pyrene induced a relatively rapid increase in intracellular Ca2+-concentrations ([Ca2+]i) in human microvascular endothelial cells (HMEC-1) and human embryonic kidney cells (HEK293) that was attenuated by AhR-inhibitor treatment and/or transient AhR knockdown by RNAi. In silico molecular docking based on homology models, suggested that pyrene is not able to bind to the human AhR in the agonist conformation. Instead, pyrene docked in the antagonist conformation of the AhR PAS-B binding pocket, although the interaction differed from antagonists such as GNF-351 and CH223191. Accordingly, pyrene did not induce CYP1A1 or CYP1B1, but suppressed CYP1-expression by benzo[a]pyrene (B[a]P) in HMEC-1 cells, confirming that pyrene act as an antagonist of AhR-induced gene expression. Use of pharmacological inhibitors and Ca2+-free medium indicated that the pyrene-induced AhR nongenomic [Ca2+]i increase was initiated by Ca2+-release from intracellular stores followed by a later phase of extracellular Ca2+-influx, consistent with store operated calcium entry (SOCE). These effects was accompanied by an AhR-dependent reduction in ordered membrane lipid domains, as determined by di-4-ANEPPDHQ staining. Addition of cholesterol inhibited both the pyrene-induced [Ca2+]i-increase and alterations in membrane lipid order. In conclusion, we propose that pyrene binds to AhR, act as an antagonist of the canonical genomic AhR/Arnt/CYP1-pathway, reduces ordered membrane lipid domains, and activates AhR nongenomic Ca2+-signaling from intracellular stores." @default.
- W2893863934 created "2018-10-05" @default.
- W2893863934 creator A5010012417 @default.
- W2893863934 creator A5012556210 @default.
- W2893863934 creator A5017383994 @default.
- W2893863934 creator A5031978455 @default.
- W2893863934 creator A5050726126 @default.
- W2893863934 creator A5054140824 @default.
- W2893863934 creator A5056517514 @default.
- W2893863934 creator A5061687512 @default.
- W2893863934 creator A5063447840 @default.
- W2893863934 creator A5091873648 @default.
- W2893863934 date "2018-12-01" @default.
- W2893863934 modified "2023-09-30" @default.
- W2893863934 title "Evidence of selective activation of aryl hydrocarbon receptor nongenomic calcium signaling by pyrene" @default.
- W2893863934 cites W1494420910 @default.
- W2893863934 cites W1935479846 @default.
- W2893863934 cites W1963612766 @default.
- W2893863934 cites W1966594837 @default.
- W2893863934 cites W1973113456 @default.
- W2893863934 cites W1979787038 @default.
- W2893863934 cites W1980358526 @default.
- W2893863934 cites W1983612873 @default.
- W2893863934 cites W1986882200 @default.
- W2893863934 cites W1989652405 @default.
- W2893863934 cites W1992427628 @default.
- W2893863934 cites W1995055722 @default.
- W2893863934 cites W2000708353 @default.
- W2893863934 cites W2002667904 @default.
- W2893863934 cites W2005855834 @default.
- W2893863934 cites W2008925541 @default.
- W2893863934 cites W2009509624 @default.
- W2893863934 cites W2012480853 @default.
- W2893863934 cites W2014781687 @default.
- W2893863934 cites W2028415142 @default.
- W2893863934 cites W2030445630 @default.
- W2893863934 cites W2032453591 @default.
- W2893863934 cites W2032770343 @default.
- W2893863934 cites W2036536542 @default.
- W2893863934 cites W2037639963 @default.
- W2893863934 cites W2047878721 @default.
- W2893863934 cites W2052140378 @default.
- W2893863934 cites W2052519626 @default.
- W2893863934 cites W2058535289 @default.
- W2893863934 cites W2062909384 @default.
- W2893863934 cites W2064169979 @default.
- W2893863934 cites W2070617809 @default.
- W2893863934 cites W2071573213 @default.
- W2893863934 cites W2071577234 @default.
- W2893863934 cites W2074777341 @default.
- W2893863934 cites W2085798235 @default.
- W2893863934 cites W2086510006 @default.
- W2893863934 cites W2088241167 @default.
- W2893863934 cites W2095249724 @default.
- W2893863934 cites W2095511031 @default.
- W2893863934 cites W2109440685 @default.
- W2893863934 cites W2127624625 @default.
- W2893863934 cites W2136650702 @default.
- W2893863934 cites W2137467707 @default.
- W2893863934 cites W2151443708 @default.
- W2893863934 cites W2156884339 @default.
- W2893863934 cites W2162483141 @default.
- W2893863934 cites W2163818502 @default.
- W2893863934 cites W2164402812 @default.
- W2893863934 cites W2170025066 @default.
- W2893863934 cites W2217899903 @default.
- W2893863934 cites W2527670917 @default.
- W2893863934 cites W2544894048 @default.
- W2893863934 cites W2801907230 @default.
- W2893863934 cites W2953316160 @default.
- W2893863934 cites W4255760236 @default.
- W2893863934 doi "https://doi.org/10.1016/j.bcp.2018.09.023" @default.
- W2893863934 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30248327" @default.
- W2893863934 hasPublicationYear "2018" @default.
- W2893863934 type Work @default.
- W2893863934 sameAs 2893863934 @default.
- W2893863934 citedByCount "18" @default.
- W2893863934 countsByYear W28938639342019 @default.
- W2893863934 countsByYear W28938639342020 @default.
- W2893863934 countsByYear W28938639342021 @default.
- W2893863934 countsByYear W28938639342022 @default.
- W2893863934 countsByYear W28938639342023 @default.
- W2893863934 crossrefType "journal-article" @default.
- W2893863934 hasAuthorship W2893863934A5010012417 @default.
- W2893863934 hasAuthorship W2893863934A5012556210 @default.
- W2893863934 hasAuthorship W2893863934A5017383994 @default.
- W2893863934 hasAuthorship W2893863934A5031978455 @default.
- W2893863934 hasAuthorship W2893863934A5050726126 @default.
- W2893863934 hasAuthorship W2893863934A5054140824 @default.
- W2893863934 hasAuthorship W2893863934A5056517514 @default.
- W2893863934 hasAuthorship W2893863934A5061687512 @default.
- W2893863934 hasAuthorship W2893863934A5063447840 @default.
- W2893863934 hasAuthorship W2893863934A5091873648 @default.
- W2893863934 hasBestOaLocation W28938639342 @default.
- W2893863934 hasConcept C104317684 @default.
- W2893863934 hasConcept C155164980 @default.
- W2893863934 hasConcept C155701950 @default.
- W2893863934 hasConcept C170493617 @default.