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dc.contributor.authorLin, Yi-Chunen_US
dc.contributor.authorHuang, Yi-Chunen_US
dc.contributor.authorWang, Yu-Shanen_US
dc.contributor.authorJuang, Rong-Huayen_US
dc.contributor.authorLiao, Kuang-Wenen_US
dc.contributor.authorChu, Rea-Minen_US
dc.date.accessioned2014-12-08T15:07:24Z-
dc.date.available2014-12-08T15:07:24Z-
dc.date.issued2010-02-15en_US
dc.identifier.issn0165-2427en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.vetimm.2009.07.013en_US
dc.identifier.urihttp://hdl.handle.net/11536/5838-
dc.description.abstractNatural killer (NK) cells have been considered to be a group of lymphocytes lacking clonally distributed receptors for antigens typical of T cells and B cells. in some mammalian species, including humans, a subpopulation of CD8(+) peripheral blood lymphocytes (PBLs) exhibits NK activity. This NK subpopulation has not been well characterized in mammals and its characterization is particularly poor in the dog. In this study, we demonstrated that a subset of canine CD8(+) cells derived from PBLs and lymphokine (IL-2)-activated killers (LAKs) of PBLs that was CD3(+), CD4(-), CD21(-), CD5(lo), alpha/beta TCR(+), and gamma/delta TCR(-) contained substantially higher levels of mRNAs for NK cell-related receptors (NKp30, NKp44, NKG2D, 2B4, and CD16 for PBL, and NKG2D and CD56 for LAK) than the corresponding CD8(-) cells. This subset of CD8(+) lymphocytes derived from LAKs also displayed significantly higher NK cytotoxic activity than the corresponding CD8(+) cells. In contrast, CD8(+) cells derived from nonstimulated PBLs showed very low levels of NK cytotoxic activity. Our results indicate that, in IL-2-stimulated PBLs, canine CD8(+) cells are an important subset associated with NK cytotoxic activity. (C) 2009 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectNK cellen_US
dc.subjectCanineen_US
dc.subjectNKp30en_US
dc.subjectCD8(+)en_US
dc.subjectCytotoxicityen_US
dc.titleCanine CD8 T cells showing NK cytotoxic activity express mRNAs for NK cell-associated surface moleculesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.vetimm.2009.07.013en_US
dc.identifier.journalVETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGYen_US
dc.citation.volume133en_US
dc.citation.issue2-4en_US
dc.citation.spage144en_US
dc.citation.epage153en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000273904500007-
dc.citation.woscount9-
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