IL-15 activates telomerase and minimizes telomere loss and may preserve the replicative life span of memory CD8+ T cells in vitiro

被引:51
|
作者
Li, Y [1 ]
Zhi, W [1 ]
Wareski, P [1 ]
Weng, NP [1 ]
机构
[1] NIA, Immunol Lab, NIH, Baltimore, MD 21224 USA
来源
JOURNAL OF IMMUNOLOGY | 2005年 / 174卷 / 07期
关键词
D O I
10.4049/jimmunol.174.7.4019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The preservation of the replicative life span of memory CD8(+) T cells is vital for long-term immune protection. Although IL-15 plays a key role in the homeostasis of memory CD8(+) T cells, it is unknown whether IL-15 regulates the replicative life span of memory CD8(+) T cells. In this study, we report an analysis of telomerase expression and telomere length in human memory phenotype CD8(+) T cells maintained by IL-15 in vitro. We demonstrate that IL-15 is capable of activating telomerase in memory CD8(+) T cells via Jak3 and PI3K signaling pathways..;urthermore, IL-15 induces a sustained level of telomerase activity over long periods of time, and in turn minimizes telomere loss ii memory CD8(+) T cells after substantial cell divisions. These findings suggest that IL-15 activates stable telomerase expression art I compensates telomere loss in memory phenotype CD8(+) T cells, and that telornerase may play anJimportant role in memory CD8(+) T cell homeostasis.
引用
收藏
页码:4019 / 4024
页数:6
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