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dc.contributor.authorTseng, Wenche
dc.contributor.authorThein, Thuzar
dc.contributor.authorKinnunen, Kati
dc.contributor.authorLashkari, Kameran
dc.contributor.authorGregory, Meredith S.
dc.contributor.authorD'Amore, Patricia Ann
dc.contributor.authorKsander, Bruce R.
dc.date.accessioned2018-03-07T19:02:17Z
dc.date.issued2013
dc.identifierQuick submit: 2017-06-23T14:59:03-0400
dc.identifier.citationTseng, Wen Allen, Thuzar Thein, Kati Kinnunen, Kameran Lashkari, Meredith S. Gregory, Patricia A. D’Amore, and Bruce R. Ksander. 2013. “NLRP3 Inflammasome Activation in Retinal Pigment Epithelial Cells by Lysosomal Destabilization: Implications for Age-Related Macular Degeneration.” Investigative Opthalmology & Visual Science 54 (1) (January 7): 110. doi:10.1167/iovs.12-10655.en_US
dc.identifier.issn1552-5783en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:34902780
dc.description.abstractPurpose.: To evaluate the effect of lysosomal destabilization on NLRP3 inflammasome activation in RPE cells and to investigate the mechanisms by which inflammasome activation may contribute to the pathogenesis of age-related macular degeneration (AMD). Methods.: Human ocular tissue sections from patients with geographic atrophy or neovascular AMD were stained for NLRP3 and compared to tissues from age-matched controls. Expression of the IL-1β precursor, pro-IL-1β, was induced in ARPE-19 cells by IL-1α treatment. Immunoblotting was performed to assess expression of NLRP3 inflammasome components (NLRP3, ASC, and procaspase-1) and pro-IL-1β in ARPE-19 cells. Lysosomes were destabilized using the lysosomotropic agent L-leucyl-L-leucine methyl ester (Leu-Leu-OMe). Active caspase-1 was detected using FAM-YVAD-FMK, a fluorescent-labeled inhibitor of caspases (FLICA) specific for caspase-1. IL-1β was detected by immunoblotting and ELISA, and cytotoxicity was evaluated by LDH quantification. Results.: RPE of eyes affected by geographic atrophy or neovascular AMD exhibited NLRP3 staining at lesion sites. ARPE-19 cells were found to express NLRP3, ASC, and procaspase-1. IL-1α dose-dependently induced pro-IL-1β expression in ARPE-19 cells. Lysosomal destabilization induced by Leu-Leu-OMe triggered caspase-1 activation, IL-1β secretion, and ARPE-19 cell death. Blocking Leu-Leu-OMe–induced lysosomal disruption with the compound Gly-Phe-CHN2 or inhibiting caspase-1 with Z-YVAD-FMK abrogated IL-1β release and ARPE-19 cytotoxicity. Conclusions.: NLRP3 upregulation occurs in the RPE during the pathogenesis of advanced AMD, in both geographic atrophy and neovascular AMD. Destabilization of RPE lysosomes induces NLRP3 inflammasome activation, which may contribute to AMD pathology through the release of the proinflammatory cytokine IL-1β and through caspase-1-mediated cell death, known as “pyroptosis.”en_US
dc.language.isoen_USen_US
dc.publisherAssociation for Research in Vision and Ophthalmology (ARVO)en_US
dc.relation.isversionof10.1167/iovs.12-10655en_US
dc.relation.hasversionhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544415/en_US
dash.licenseLAA
dc.titleNLRP3 Inflammasome Activation in Retinal Pigment Epithelial Cells by Lysosomal Destabilization: Implications for Age-Related Macular Degenerationen_US
dc.typeJournal Articleen_US
dc.date.updated2017-06-23T18:59:06Z
dc.description.versionVersion of Recorden_US
dc.relation.journalInvestigative Opthalmology & Visual Scienceen_US
dash.depositing.authorD'Amore, Patricia Ann
dc.date.available2013
dc.date.available2018-03-07T19:02:17Z
dc.identifier.doi10.1167/iovs.12-10655*
dash.authorsorderedfalse
dash.contributor.affiliatedThein, Thuzar
dash.contributor.affiliatedTseng, Wenche
dash.contributor.affiliatedLashkari, Kameran
dash.contributor.affiliatedKsander, Bruce
dash.contributor.affiliatedD'Amore, Patricia


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