期刊
CELLULAR IMMUNOLOGY
卷 250, 期 1-2, 页码 68-74出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.cellimm.2008.01.006
关键词
Tim-3; galectin-9; CD8; cytotoxic; apoptosis
CD8(+) alloreactive T cells are the key mediators of accelerated rejection. Vigorous CD8(+) alloreactive T cells responses against alloantigens, which is the main effector mechanism in acute allograft rejection, has been well described. But the molecular mechanisms to dampen activated CD8(+) T cells are largely unknown. On the other hand, Tim-3 is a molecule expressed on terminally differentiated CD4(+) Th1 cells. Engaging Tim-3 with its ligand galectin-9 causes an inhibitory signal, resulting in apoptosis of Th1 cells and negatively regulates Th I type immunity. However, the question whether CD8(+) T cells express surface molecular Tim-3 has not been fully elucidated. In this study, we have investigated which CD8(+) subset express molecular Tim-3 by flow cytometric assay. In addition, cytotoxic assay was applied to analyze whether CD8(+) alloreactive T cells were sensitive to galectin-9 induced apoptosis. Here, our results demonstrated that Tim-3 was expressed on activated CD8(+) alloreactive T cells (CD8(+)CD44(high)CD62L(low)), but not expressed on naive CD8(+) T cells. Furthermore, alloreactive CD8(+) cytotoxic T cells were sensitive to galectin-9 induced apoptosis both in vitro and vivo, resulting in attenuation of CD8(+) alloreactive T cells mediated cytotoxicity and prolonged survival of skin graft. (c) 2008 Elsevier Inc. All rights reserved.
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