APOPTOSIS - MOLECULAR CONTROL POINT IN TOXICITY

被引:227
作者
CORCORAN, GB
FIX, L
JONES, DP
MOSLEN, MT
NICOTERA, P
OBERHAMMER, FA
BUTTYAN, R
机构
[1] FRITO LAY INC, RES DEPT, IRVING, TX 75061 USA
[2] EMORY UNIV, SCH MED, DEPT BIOCHEM, ATLANTA, GA 30322 USA
[3] UNIV TEXAS, MED BRANCH, DEPT PATHOL, GALVESTON, TX 77550 USA
[4] KAROLINSKA INST, DEPT TOXICOL, STOCKHOLM, SWEDEN
[5] UNIV VIENNA, INST TUMOR BIOL, VIENNA, AUSTRIA
[6] COLUMBIA UNIV, COLL PHYS & SURG, DEPT UROL, NEW YORK, NY 10031 USA
关键词
D O I
10.1006/taap.1994.1195
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Apoptosis is a controlled form of cell death that serves as a molecular point of regulation for biological processes. Cell selection by apoptosis occurs during normal physiological functions as well as toxicities and diseases. Apoptosis is the counterpart and counterbalance to mitosis in cell population determination. Complex patterns of cell signaling and specific gene expression are clearly involved in the control of cell fate. Exposure to an apogen, a trigger of apoptosis, can significantly increase apoptotic cell loss during homeostatic processes as well as acute or chronic toxicities. Alternately, suppression of apoptosis through, for example, interference in cell signaling can result in pathological accumulation of aberrant cells and diseases such as tumors. Investigations into the mechanisms underlying apoptosis have extended into many areas, driven by increasingly sophisticated instrumental and molecular biology techniques. This symposium summary explores related aspects of apoptosis, including control of cell population size and function, specific gene activity and regulation, chromatin condensation and scaffold detachment, oxidative stress-induced cell proliferation versus death by apoptosis or necrosis, and hepatotoxicant-induced apoptosis versus necrosis. Insights into the mechanisms governing apoptosis and increasing appreciation of the relevance of apoptotic cell death are redirecting research in toxicology and carcinogenesis and are yielding novel therapeutic approaches for the control of toxicity, disease, and ultimately perhaps senescence. (C) 1994 Academic Press, Inc.
引用
收藏
页码:169 / 181
页数:13
相关论文
共 100 条
  • [1] PREFERENTIAL, COOPERATIVE BINDING OF DNA TOPOISOMERASE-II TO SCAFFOLD-ASSOCIATED REGIONS
    ADACHI, Y
    KAS, E
    LAEMMLI, UK
    [J]. EMBO JOURNAL, 1989, 8 (13) : 3997 - 4006
  • [2] APOPTOSIS - A GENERAL COMMENT
    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
    [J]. FASEB JOURNAL, 1991, 5 (08) : 2127 - 2128
  • [3] ALNEMRI ES, 1989, J BIOL CHEM, V264, P4104
  • [4] ARENDS MJ, 1990, AM J PATHOL, V136, P593
  • [5] ASKEW DS, 1991, ONCOGENE, V6, P1915
  • [6] CHARACTERIZATION OF THE PRODUCTS OF A GENE EXPRESSED DURING ANDROGEN-PROGRAMMED CELL-DEATH AND THEIR POTENTIAL USE AS A MARKER OF UROGENITAL INJURY
    BANDYK, MG
    SAWCZUK, IS
    OLSSON, CA
    KATZ, AE
    BUTTYAN, R
    [J]. JOURNAL OF UROLOGY, 1990, 143 (02) : 407 - 413
  • [7] ENDONUCLEASE ACTIVATION DURING APOPTOSIS - THE ROLE OF CYTOSOLIC CA2+ AND PH
    BARRY, MA
    EASTMAN, A
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 186 (02) : 782 - 789
  • [8] BELLOMO G, 1992, CANCER RES, V52, P1342
  • [9] THE PROTEIN PHOSPHATASE INHIBITOR OKADAIC ACID INDUCES MORPHOLOGICAL-CHANGES TYPICAL OF APOPTOSIS IN MAMMALIAN-CELLS
    BOE, R
    GJERTSEN, BT
    VINTERMYR, OK
    HOUGE, G
    LANOTTE, M
    DOSKELAND, SO
    [J]. EXPERIMENTAL CELL RESEARCH, 1991, 195 (01) : 237 - 246
  • [10] BCL-X, A BCL-2-RELATED GENE THAT FUNCTIONS AS A DOMINANT REGULATOR OF APOPTOTIC CELL-DEATH
    BOISE, LH
    GONZALEZGARCIA, M
    POSTEMA, CE
    DING, LY
    LINDSTEN, T
    TURKA, LA
    MAO, XH
    NUNEZ, G
    THOMPSON, CB
    [J]. CELL, 1993, 74 (04) : 597 - 608