Reactive oxygen species participate in peroxynitrite-induced apoptosis in HL-60 cells

被引:103
作者
Lin, KT
Xue, JY
Sun, FF
Wong, PYK
机构
[1] UNIV MED & DENT NEW JERSEY, SCH OSTEOPATH MED, DEPT CELL BIOL, STRATFORD, NJ 08084 USA
[2] UNIV MED & DENT NEW JERSEY, ROBERT WOOD JOHNSON MED SCH, DEPT MOL GENET & MICROBIOL, PISCATAWAY, NJ 08854 USA
关键词
D O I
10.1006/bbrc.1996.5897
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Peroxynitrite (ONOO-) is a physiological product generated by the interaction of superoxide (O-2(.-)) and nitric oxide ((NO)-N-.), We have previously shown that peroxynitrite induces apoptosis in HL-60 cells, In the present study, we demonstrated that peroxynitrite generates reactive oxygen species (ROS) in HL-60 cells, Brief exposure of HL-60 cells to ONOO- induced elevation of lucigenin chemiluminescence, indicating generation of superoxide anion. Exogenous superoxide dismutase (SOD), a scavenger of O-2(.-), fully abolished the chemiluminescence response, further supporting this notion. Following O-2(.-) generation, the accumulation of hydrogen peroxide (H2O2) was observed, The addition of SOD exacerbated but that of catalase attenuated peroxynitrite-induced DNA fragmentation, suggesting that this H2O2 production contributes to the apoptotic process, In addition, pre-treatment of HL-60 cells with N-acetyl-L-cysteine (15 mM), a ROS scavenger, fully scavenged peroxynitrite-elicited ROS generation and effectively inhibited ONOO--induced apoptosis, further enforcing this hypothesis, In summary, our results suggest that ONOO--stimulated ROS formation may serve as a mechanism for the propagation of peroxynitrite-mediated apoptotic cell death in an intact cell system. (C) 1997 Academic Press
引用
收藏
页码:115 / 119
页数:5
相关论文
共 31 条
[1]  
ALLEN RC, 1986, METHOD ENZYMOL, V133, P449
[2]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[3]   EXTENSIVE NITRATION OF PROTEIN TYROSINES IN HUMAN ATHEROSCLEROSIS DETECTED BY IMMUNOHISTOCHEMISTRY [J].
BECKMANN, JS ;
YE, YZ ;
ANDERSON, PG ;
CHEN, J ;
ACCAVITTI, MA ;
TARPEY, MM ;
WHITE, CR ;
BECKMAN, JS .
BIOLOGICAL CHEMISTRY HOPPE-SEYLER, 1994, 375 (02) :81-88
[5]   SUPEROXIDE ANION INHIBITS CGMP-ASSOCIATED BOVINE PULMONARY ARTERIAL RELAXATION [J].
CHERRY, PD ;
OMAR, HA ;
FARRELL, KA ;
STUART, JS ;
WOLIN, MS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 259 (04) :H1056-H1062
[6]   BIOLOGICAL EFFECTS OF THE SUPEROXIDE RADICAL [J].
FRIDOVICH, I .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1986, 247 (01) :1-11
[7]  
Gutteridge J. M. C., 1989, FREE RADICALS BIOL M
[8]   LUCIGENIN CHEMILUMINESCENCE IN THE ASSESSMENT OF NEUTROPHIL SUPEROXIDE PRODUCTION [J].
GYLLENHAMMAR, H .
JOURNAL OF IMMUNOLOGICAL METHODS, 1987, 97 (02) :209-213
[9]  
HIRAISHI H, 1992, J BIOL CHEM, V267, P14812
[10]   THE REACTION OF NO WITH SUPEROXIDE [J].
HUIE, RE ;
PADMAJA, S .
FREE RADICAL RESEARCH COMMUNICATIONS, 1993, 18 (04) :195-199