CD8+T cells in large granular lymphocyte leukemia are not defective in activation- and replication-related apoptosis

被引:18
作者
Melenhorst, JJ
Brümmendorf, TH
Kirby, M
Lansdorp, PM
Barrett, AJ
机构
[1] NHLBI, Bone Marrow Transplant Unit, Hematol Branch, NIH, Bethesda, MD 20892 USA
[2] British Columbia Canc Res Ctr, Terry Fox Lab, Vancouver, BC V5Z 1L3, Canada
关键词
LGL; apoptosis; telomere; flow-FISH; homeostasis; Fas;
D O I
10.1016/S0145-2126(01)00010-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Persistent lymphocytosis in large granular lymphocyte leukemia (LGL) may result from defects in activation- or Fas crosslinking-induced cell death. Here we show that Fas crosslinking and CD3 activation causes apoptosis of in vitro activated CD8 T cells, but not of freshly isolated CD8 T cells. Death was partially blocked by a neutralizing antibody to FasL. Inhibition of metalloproteinase-mediated FasL solubilization significantly potentiated induction of cell death. Further-more, CD3 plus CD28 stimulation resulted in telomeric erosion in LGL cells, and ultimately proliferation ceased. Together, these data indicate that activation- and proliferation-related cell death mechanisms are functional in LGL cells. Published by Elsevier Science Ltd.
引用
收藏
页码:699 / 708
页数:10
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