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Responses of Multipotent Retinal Stem Cells to IL-1 β,IL-18,or IL-17
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نویسنده
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chen s. ,shen d. ,popp n.a. ,ogilvy a.j. ,tuo j. ,abu-asab m. ,xie t. ,chan c.-c.
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منبع
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journal of ophthalmology - 2015 - دوره : 2015 - شماره : 0
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چکیده
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Purpose. to investigate how multipotent retinal stem cells (rscs) isolated from mice respond to the proinflammatory signaling molecules,il-1β,il-18,and il-17a. materials and methods. rscs were cultured in a specific culture medium and were treated with these cytokines. cell viability was detected by mtt assay; ultrastructure was evaluated by transmission electron microscopy; expression of il-17rc and proapoptotic proteins was detected by immunocytochemistry and expression of il-6 and il-17a was detected by quantitative rt-pcr. as a comparison,primary mouse retinal pigment epithelium (rpe) cells were also treated with il-1β,il-18,or il-17a and analyzed for the expression of il-6 and il-17rc. results. treatment with il-1β,il-18,or il-17a decreased rsc viability in a dose-dependent fashion and led to damage in cellular ultrastructure including pyroptotic and/or necroptotic cells. il-1β and il-18 could induce proapoptotic protein expression. all treatments induced significantly higher expression of il-6 and il-17rc in both cells. however,neither il-1β nor il-18 could induce il-17a expression in rscs. conclusions. il-1β,il-18,and il-17a induce retinal cell death via pyroptosis/necroptosis and apoptosis. they also provoke proinflammatory responses in rscs. though il-1β and il-18 could not induce il-17a expression in rscs,they both increase il-17rc expression,which may mediate the effect of il-17a. © 2015 shida chen et al.
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آدرس
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laboratory of immunology,national eye institute,national institutes of health,bethesda, United States, laboratory of immunology,national eye institute,national institutes of health,bethesda, United States, laboratory of immunology,national eye institute,national institutes of health,bethesda, United States, histology core,national eye institute,national institutes of health,bethesda, United States, zhongshan ophthalmic center,sun yat-sen university, China, histology core,national eye institute,national institutes of health,bethesda, United States, stowers institute for medical research,kansas city, United States, department of anatomy and cell biology,university of kansas school of medicine,kansas city, United States
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Authors
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