Full metadata record

DC FieldValueLanguage
dc.contributor.author최제민-
dc.date.accessioned2016-10-12T01:24:02Z-
dc.date.available2016-10-12T01:24:02Z-
dc.date.issued2015-04-
dc.identifier.citationINTERNATIONAL IMMUNOPHARMACOLOGY, v. 25, NO 2, Page. 285-292en_US
dc.identifier.issn1567-5769-
dc.identifier.issn1878-1705-
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S1567576915000466-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/23763-
dc.description.abstractPiceatannol, a metabolite of resveratrol found in red wine and grapes, displays a wide spectrum of biological activity. Although the anti-oxidant, anti-inflammatory, and anti-tumorigenesis activity of piceatannol has been extensively studied, its role in the adaptive immune response has received less attention. Here we investigated the role of piceatannol, a well-known Syk inhibitor, in T cell activation, proliferation, and differentiation using isolated murine splenic T cells from C57BL/6 mice. Piceatannol treatment inhibited surface expression of CD4 and CD8 T cell activation markers CD25 and CD69, reduced production of cytokines IFN gamma, IL-2, and IL-17, and suppressed proliferation of activated T cells. Moreover, piceatannol treatment significantly inhibited differentiation of CD4(+)CD25(-)CD62L(+) naive CD4 T cells into Th1, Th2, and Th17 cells, presumably due to inhibition of TcR signaling through p-Erk, p-Akt, and p-p38. Piceatannol appears to be a useful nutritional or pharmacological biomolecule that regulates effector T cell functions such as cytokine production, differentiation, and proliferation. (C) 2015 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipThis study is supported by the Basic Science Research Program through the grants from the National Research Foundation of Korea (NRF-2013R1A1A2A10060048) and Hanyang University (HY-2011-00000001004).en_US
dc.language.isoenen_US
dc.publisherELSEVIER SCIENCE BVen_US
dc.subjectPiceatannolen_US
dc.subjectT cellsen_US
dc.subjectTcR signalingen_US
dc.subjectT cell proliferationen_US
dc.subjectT cell differentiationen_US
dc.titlePiceatannol inhibits effector T cell functions by suppressing TcR signalingen_US
dc.typeArticleen_US
dc.relation.no2-
dc.relation.volume25-
dc.identifier.doi10.1016/j.intimp.2015.01.030-
dc.relation.page285-292-
dc.relation.journalINTERNATIONAL IMMUNOPHARMACOLOGY-
dc.contributor.googleauthorKim, Do-Hyun-
dc.contributor.googleauthorLee, Yong-Gab-
dc.contributor.googleauthorPark, Hong-Jai-
dc.contributor.googleauthorLee, Jung-Ah-
dc.contributor.googleauthorKim, Hyun Jung-
dc.contributor.googleauthorHwang, Jae-Kwan-
dc.contributor.googleauthorChoi, Je-Min)-
dc.relation.code2015002418-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF LIFE SCIENCE-
dc.identifier.pidjeminchoi-
Appears in Collections:
COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > LIFE SCIENCE(생명과학과) > Articles
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML


qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE