DNA FRAGMENTATION INDUCED BY CYTOTOXIC T-LYMPHOCYTES CAN RESULT IN TARGET-CELL DEATH

被引:25
作者
HELGASON, CD
SHI, LF
GREENBERG, AH
SHI, YF
BROMLEY, P
COTTER, TG
GREEN, DR
BLEACKLEY, RC
机构
[1] UNIV ALBERTA, DEPT BIOCHEM, EDMONTON T6G 2H7, ALBERTA, CANADA
[2] UNIV MANITOBA, DEPT IMMUNOL, WINNIPEG R3E 0V9, MANITOBA, CANADA
[3] UNIV MANITOBA, MANITOBA INST CELL BIOL, WINNIPEG R3E 0V9, MANITOBA, CANADA
[4] LA JOLLA INST ALLERGY & IMMUNOL, LA JOLLA, CA 92037 USA
[5] UNIV ALBERTA, DEPT IMMUNOL, EDMONTON T6G 2H7, ALBERTA, CANADA
关键词
D O I
10.1006/excr.1993.1150
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cytotoxic T lymphocyte (CTL)-mediated lysis is accompanied by fragmentation of target cell DNA into an oligonuclcosome ladder, a hallmark of apoptosis. Is this a fortuitous coincidence, or could CTL be inducing lysis by activation of the suicide signal? In this report we demonstrate that CTL-mediated target cell death can be blocked with the drug aurintricarboxylic acid (ATA). The abrogation of death correlates with the inhibition of DNA fragmentation. While ATA prevented DNA fragmentation, it failed to significantly alter protein, RNA, or DNA synthesis in the cell lines over the dose range used. In addition, there was no inhibition of cell-cell interaction or granule exocytosis during CTL-mediated killing. ATA also significantly inhibited the cytolysis and DNA fragmentation mediated by isolated cytolytic granules, as well as the granular protein fragmentin. We developed an assay in which target cells could be separated from CTL after binding and programming for lysis. Once they had received the “kiss of death,” target cells could be rescued from lysis (as indicated by inhibition of DNA fragmentation and increased target cell viability) by treatment with ATA. These results suggest that ATA blocks target cell death by inhibition of DNA fragmentation, and further, that chromatin degradation is a cause rather than a result of cell death in CTL-mediated lysis. © 1993 Academic Press, Inc.
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页码:302 / 310
页数:9
相关论文
共 47 条
[1]   AURINTRICARBOXYLIC ACID RESCUES PC12 CELLS AND SYMPATHETIC NEURONS FROM CELL-DEATH CAUSED BY NERVE GROWTH-FACTOR DEPRIVATION - CORRELATION WITH SUPPRESSION OF ENDONUCLEASE ACTIVITY [J].
BATISTATOU, A ;
GREENE, LA .
JOURNAL OF CELL BIOLOGY, 1991, 115 (02) :461-471
[2]  
BERKE G, 1987, TRANSPLANT P, V19, P412
[3]  
COHEN JJ, 1984, J IMMUNOL, V132, P38
[4]   EFFECTS OF CYCLOHEXIMIDE ON B-CHRONIC LYMPHOCYTIC LEUKEMIC AND NORMAL LYMPHOCYTES INVITRO - INDUCTION OF APOPTOSIS [J].
COLLINS, RJ ;
HARMON, BV ;
SOUVLIS, T ;
POPE, JH ;
KERR, JFR .
BRITISH JOURNAL OF CANCER, 1991, 64 (03) :518-522
[5]   MEMBRANOLYTIC AND NUCLEOLYTIC ACTIVITIES OF CYTOLYTIC LYMPHOCYTE-T CLONES [J].
COSGROVE, JM ;
HOWCROFT, TK ;
TATUM, SM ;
LINDQUIST, RR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 179 (03) :1562-1567
[6]  
DENNERT G, 1988, J IMMUNOL, V141, P785
[7]   PURIFIED PERFORIN INDUCES TARGET-CELL LYSIS BUT NOT DNA FRAGMENTATION [J].
DUKE, RC ;
PERSECHINI, PM ;
CHANG, S ;
LIU, CC ;
COHEN, JJ ;
YOUNG, JDE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (04) :1451-1456
[8]   ENDOGENOUS ENDONUCLEASE-INDUCED DNA FRAGMENTATION - AN EARLY EVENT IN CELL-MEDIATED CYTOLYSIS [J].
DUKE, RC ;
CHERVENAK, R ;
COHEN, JJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (20) :6361-6365
[9]  
DUKE RC, 1989, CELLULAR BASIS IMMUN, P311
[10]   CELL-DEATH MECHANISMS AND THE IMMUNE-SYSTEM [J].
GOLSTEIN, P ;
OJCIUS, DM ;
YOUNG, JDE .
IMMUNOLOGICAL REVIEWS, 1991, 121 :29-65