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dc.contributor.authorChang, Qing
dc.contributor.authorPeter, Marcus E.
dc.contributor.authorGrassi, Michael A.
dc.date.accessioned2013-11-22T15:28:55Z
dc.date.available2013-11-22T15:28:55Z
dc.date.issued2012-06
dc.identifier.bibliographicCitationChang Q, Peter ME, Grassi MA. Fas ligand-Fas signaling participates in light-induced apoptotic death in photoreceptor cells. Investigative Ophthalmology & Visual Science. 2012 Jun 20;53(7):3703-16.doi: 10.1167/iovs.11-8928en_US
dc.identifier.issn1552-5783
dc.identifier.urihttp://hdl.handle.net/10027/10588
dc.descriptionPost print version of article may differ from published version. The definitive version is available through Association for Research in Vision and Ophthalmology at DOI:10.1167/iovs.11-8928en_US
dc.description.abstractPURPOSE. To investigate the function of Fas in photoreceptors. METHODS. Postmortem human eyes and mouse-derived photoreceptor cells (661W) were examined for Fas expression by in situ hybridization and immunofluorescence. 661W cells were treated with FasL, Fas agonistic antibody, or exposed to light with/without pharmacological manipulation of Fas signaling, followed by apoptosis detection by TUNEL, immunofluorescence and FACS. Fractionated cellular extracts were used to detect protein expression or protein phosphorylation after immunoprecipitation by western blot. RESULTS. Expression of Fas was found in the photoreceptor layer of human retina. Fas and a cleaved form of FasL were found on the cell surface of 661W cells. Treatment with FasL or Fas agonistic antibody induced apoptosis in 661W cells. Blocking the activity of FasL or administration of caspase-8 inhibitor z-IETD inhibited light-induced apoptosis. However, it simultaneously caused induction of necroptosis, which could be blocked by the RIP1 inhibitor, Necrostatin-1. Light exposure in the presence of z-IETD caused hyper-phosphorylation of RIP1. Light exposure did not elevate the expression of Fas, FasL, or FADD. Cells or conditioned medium after light exposure induced apoptosis in dark-adapted cells, which could be attenuated by blockade of Fas. CONCLUSIONS. Fas has a pro-apoptotic role in photoreceptors. Under light stress, soluble and 2 membrane-bound FasL can bind to Fas inducing apoptosis via a paracrine mechanism. Although blocking Fas signaling inhibits apoptosis, it does not improve the overall photoreceptor survival due to a compensatory activation of necroptosis. Hence, prevention of photoreceptor loss from retinal photooxidative stress should target both Fas and RIP1.en_US
dc.language.isoen_USen_US
dc.publisherAssociation for Research in Vision and Ophthalmologyen_US
dc.titleFas Ligand-Fas Signaling Participates in Light-Induced Apoptotic Death in Photoreceptor Cellsen_US
dc.typeArticleen_US


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