FORMATION OF APOPTOTIC BODIES IS ASSOCIATED WITH INTERNUCLEOSOMAL DNA FRAGMENTATION DURING DRUG-INDUCED APOPTOSIS

被引:31
作者
CATCHPOOLE, DR [1 ]
STEWART, BW [1 ]
机构
[1] UNIV NEW S WALES, PRINCE WALES CHILDRENS HOSP, CHILDRENS LEUKAEMIA & CANC RES CTR, SYDNEY, NSW 2031, AUSTRALIA
关键词
D O I
10.1006/excr.1995.1021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The onset of apoptosis is often coincident with internucleosomal DNA fragmentation or ladders which are considered a hallmark of the process. However, several studies have indicated that MOLT-4 human lymphoblastoid cells exposed to various agents, including VP16, display some apoptotic characteristics in the absence of either internucleosomal ladders or production of apoptotic bodies. The present study records that, in the presence of aurintricarboxylic acid (ATA), internucleosomal ladders were detected in DNA isolated from VP16-treated MOLT-4 cells; a paradoxical result in view of inhibition by ATA of nuclease activity in cell free preparations. The activity of ATA in mediating genomic fragmentation was dose- and time-dependent. Moreover, addition of ATA to VP16-treated MOLT-4 cells also resulted in production of apoptotic bodies, this effect being quantified by morphological examination and flow cytometry. Detection of ladders and apoptotic bodies after addition of ATA was not attributable to increased toxicity in cells exposed to the combined treatment relative to VP16 alone. A similar response, that is the appearance of both internucleosomal fragmentation and apoptotic bodies, occurred after exposure of MOLT-4 cells to the mitotic inhibitor podophyllotoxin. The consistent association between internucleosomal fragmentation of DNA and formation of apoptotic bodies exhibited during death of MOLT-4 cells, insofar as both characteristics are either present or absent following different agents, suggests interdependence. (C) 1995 Academic Press, Inc.
引用
收藏
页码:169 / 177
页数:9
相关论文
共 55 条
[1]   APOPTOSIS - A GENERAL COMMENT [J].
ALLES, A ;
ALLEY, K ;
BARRETT, JC ;
BUTTYAN, R ;
COLUMBANO, A ;
COPE, FO ;
COPELAN, EA ;
DUKE, RC ;
FAREL, PB ;
GERSHENSON, LE ;
GOLDGABER, D ;
GREEN, DR ;
HONN, KV ;
HULLY, J ;
ISAACS, JT ;
KERR, JFR ;
KRAMMER, PH ;
LOCKSHIN, RA ;
MARTIN, DP ;
MCCONKEY, DJ ;
MICHAELSON, J ;
SCHULTEHERMANN, R ;
SERVER, AC ;
SZENDE, B ;
TOMEI, LD ;
TRITTON, TR ;
UMANSKY, SR ;
VALERIE, K ;
WARNER, HR .
FASEB JOURNAL, 1991, 5 (08) :2127-2128
[2]  
BARRY MA, 1993, CANCER RES, V53, P2349
[3]   IDENTIFICATION OF DEOXYRIBONUCLEASE-II AS AN ENDONUCLEASE INVOLVED IN APOPTOSIS [J].
BARRY, MA ;
EASTMAN, A .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 300 (01) :440-450
[4]   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
[5]  
BERTRAND R, 1991, CANCER RES, V51, P6280
[6]  
BINASTEIN M, 1976, MOL PHARMACOL, V12, P191
[7]   INHIBITION OF NUCLEIC ACID-BINDING PROTEINS BY AURINTRICARBOXYLIC ACID [J].
BLUMENTHAL, T ;
LANDERS, TA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1973, 55 (03) :680-688
[8]   THE BIOCHEMISTRY OF CELL-DEATH BY APOPTOSIS [J].
BURSCH, W ;
KLEINE, L ;
TENNISWOOD, M .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1990, 68 (09) :1071-1074
[9]  
CATCHPOOLE DR, 1993, CANCER RES, V53, P4287
[10]  
CATCHPOOLE DR, 1994, ANTICANCER RES, V14, P853