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dc.contributor.authorChang, Cicero Lee-Tianen_US
dc.contributor.authorChang, Shu-Linen_US
dc.contributor.authorLee, Yi-Meien_US
dc.contributor.authorChiang, Yi-Mingen_US
dc.contributor.authorChuang, Da-Yungen_US
dc.contributor.authorKuo, Hui-Kaien_US
dc.contributor.authorYang, Wen-Chinen_US
dc.date.accessioned2014-12-08T15:24:31Z-
dc.date.available2014-12-08T15:24:31Z-
dc.date.issued2007-06-01en_US
dc.identifier.issn0022-1767en_US
dc.identifier.urihttp://hdl.handle.net/11536/17001-
dc.description.abstractSome polyacetylenes from the plant Bidens pilosa have been reported to treat diabetes. In this study, we report that the cytopiloyne from B. pilosa, which is structurally different from the above-mentioned polyacetylenes and inhibits CD4(+) T cell proliferation, effectively prevents the development of diabetes in nonobese diabetic mice as evidenced by a normal level of blood glucose and insulin and normal pancreatic islet architecture. Cytopiloyne also suppresses the differentiation of type 1 Th cells but promotes that of type 2 Th cells, which is consistent with it enhancing GATA-3 transcription. Also, long-term application of cytopiloyne significantly decreases the level of CD4(+) T cells inside pancreatic lymph nodes and spleens but does not compromise total Ab responses mediated by T cells. Coculture assays imply that this decrease in CD4(+) T cells involves the Fas ligand/Fas pathway. Overall, our results suggest that cytopiloyne prevents type 1 diabetes mainly via T cell regulation.en_US
dc.language.isoen_USen_US
dc.titleCytopiloyne, a polyacetylenic glucoside, prevents type 1 diabetes in nonobese diabetic miceen_US
dc.typeArticleen_US
dc.identifier.journalJOURNAL OF IMMUNOLOGYen_US
dc.citation.volume178en_US
dc.citation.issue11en_US
dc.citation.spage6984en_US
dc.citation.epage6993en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000246896300040-
dc.citation.woscount21-
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