Cross-linking of P-selectin glycoprotein ligand-1 induces death of activated T cells

被引:24
作者
Chen, SC
Huang, CC
Chien, CL
Jeng, CJ
Su, HT
Chiang, E
Liu, MR
Wu, CHH
Chang, CN
Lin, RH
机构
[1] Natl Taiwan Univ, Coll Med, Dept Anat & Cell Biol, Taipei, Taiwan
[2] Natl Taiwan Univ, Coll Med, Grad Inst Immunol, Taipei, Taiwan
关键词
D O I
10.1182/blood-2003-05-1679
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Increasing evidence has shown that death signaling in T cells is regulated in a complicated way. Molecules other than death receptors can also trigger T-cell death. Here, we demonstrate for the first time that P-selectin glycoprotein ligand-1 (PSGL-1) or CD162 molecules crosslinked by an anti-PSGL-1 monoclonal antibody, TAB4, can trigger a death signal in activated T cells. In contrast to classic cell death, PSGL-1-mediated T-cell death is caspase independent. It involves translocation of apoptosis-inducing factor from mitochondria to nucleus and mitochondrial cytochrome c release. Ultrastructurally, both peripheral condensation of chromatin and apoptotic body were observed in PSGL-1-mediated T-cell death. Collectively, this study demonstrates a novel role for PSGL-1 in controlling activated T-cell death and, thus, advances our understanding of immune regulation. (C) 2004 by The American Society of Hematology.
引用
收藏
页码:3233 / 3242
页数:10
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