A distinct pathway of cell-mediated apoptosis initiated by granulysin

被引:121
作者
Kaspar, AA
Okada, S
Kumar, J
Poulain, FR
Drouvalakis, KA
Kelekar, A
Hanson, DA
Kluck, RM
Hitoshi, Y
Johnson, DE
Froelich, CJ
Thompson, CB
Newmeyer, DD
Anel, A
Clayberger, C
Krensky, AM [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Pediat, Div Immunol & Transplantat Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Cardiothorac Surg, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Mol Pharmacol, Stanford, CA 94305 USA
[4] Univ Chicago, Howard Hughes Med Inst, Gwen Knapp Ctr Lupus & Immunol Res, Chicago, IL 60637 USA
[5] La Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USA
[6] Univ Pittsburgh, Dept Med, Pittsburgh, PA 15213 USA
[7] Northwestern Univ, Evanston NW Res Inst, Evanston, IL 60201 USA
[8] Univ Penn, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[9] Univ Zaragoza, Fac Ciencias, Dept Bioquim, E-50009 Zaragoza, Spain
关键词
D O I
10.4049/jimmunol.167.1.350
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Granulysin is an antimicrobial and tumoricidal molecule expressed in granules of CTL and NK cells. In this study, we show that granulysin damages cell membranes based upon negative charge, disrupts the transmembrane potential (Delta psi) in mitochondria, and causes release of cytochrome c. Granulysin-induced apoptosis is blocked in cells overexpressing Bcl-2. Despite the release of cytochrome c, procaspase 9 is not processed. Nevertheless, activation of caspase 3 is observed in granulysin-treated cells, suggesting that granulysin activates a novel pathway of CTL- and NK cell-mediated death distinct from granzyme- and death receptor-induced apoptosis.
引用
收藏
页码:350 / 356
页数:7
相关论文
共 46 条
[1]  
ALLEY MC, 1988, CANCER RES, V48, P589
[2]   NK-LYSIN, A NOVEL EFFECTOR PEPTIDE OF CYTOTOXIC T-CELLS AND NK-CELLS - STRUCTURE AND CDNA CLONING OF THE PORCINE FORM, INDUCTION BY INTERLEUKIN-2, ANTIBACTERIAL AND ANTITUMOR-ACTIVITY [J].
ANDERSSON, M ;
GUNNE, H ;
AGERBERTH, B ;
BOMAN, A ;
BERGMAN, T ;
SILLARD, R ;
JORNVALL, H ;
MUTT, V ;
OLSSON, B ;
WIGZELL, H ;
DAGERLIND, A ;
BOMAN, HG ;
GUDMUNDSSON, GH .
EMBO JOURNAL, 1995, 14 (08) :1615-1625
[3]  
[Anonymous], 1998, RADIAT RES
[4]   Inhibition of caspase proteases by CrmA enhances the resistance of human leukemic cells to multiple chemotherapeutic agents [J].
Antoku, K ;
Liu, Z ;
Johnson, DE .
LEUKEMIA, 1997, 11 (10) :1665-1672
[5]   Death receptors: Signaling and modulation [J].
Ashkenazi, A ;
Dixit, VM .
SCIENCE, 1998, 281 (5381) :1305-1308
[6]   Granzyme A loading induces rapid cytolysis and a novel form of DNA damage independently of caspase activation [J].
Beresford, PJ ;
Xia, ZN ;
Greenberg, AH ;
Lieberman, J .
IMMUNITY, 1999, 10 (05) :585-594
[7]   THE CTLS KISS OF DEATH [J].
BERKE, G .
CELL, 1995, 81 (01) :9-12
[8]   Analysis of binding and membrane destabilization of phospholipid membranes by surfactant apoprotein B [J].
Chang, R ;
Nir, S ;
Poulain, FR .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1998, 1371 (02) :254-264
[9]   FADD, A NOVEL DEATH DOMAIN-CONTAINING PROTEIN, INTERACTS WITH THE DEATH DOMAIN OF FAS AND INITIATES APOPTOSIS [J].
CHINNAIYAN, AM ;
OROURKE, K ;
TEWARI, M ;
DIXIT, VM .
CELL, 1995, 81 (04) :505-512
[10]   ACTIVATION OF THE APOPTOTIC PROTEASE CPP32 BY CYTOTOXIC T-CELL-DERIVED GRANZYME-B [J].
DARMON, AJ ;
NICHOLSON, DW ;
BLEACKLEY, RC .
NATURE, 1995, 377 (6548) :446-448