The ASK1-MAP kinase cascades in mammalian stress response

被引:267
作者
Matsukawa, J
Matsuzawa, A
Takeda, K
Ichijo, H
机构
[1] Univ Tokyo, Lab Cell Signaling, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[2] Japan Sci & Technol Corp, CREST, Tokyo 1130033, Japan
关键词
apoptosis; ASKl; JNK; MAPKKK; p38;
D O I
10.1093/jb/mvh134
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
The mitogen-activated protein (MAP) kinase cascades play essential roles in a variety of cell processes by influencing transcriptional or translational regulation. ERKs play a central role in survival and mitogenic signaling, while JNKs and p38 MAP kinases are preferentially activated by environmental stresses and are actively involved in various stress responses including cell death, survival and differentiation. Apoptosis signal-regulating kinase 1 (ASK1)-a serine/threonine protein kinase-is a member of the MAPKKK family and activates both JNK and p38 pathways. It is well known that ASK1 is activated in cells treated with death receptor ligands and oxidant stress, such as that caused by hydrogen peroxide (H2O2). Moreover, recent studies have revealed new mechanisms by which ASK1 is activated in response to various types of extracellular and intracellular signals, such as endoplasmic reticulum (ER) stress, calcium signaling, and G-protein coupled receptor (GPCR) signaling. This review summarizes the regulatory mechanisms of ASK1 activity and the physiological roles of ASK1-mediated signal transduction.
引用
收藏
页码:261 / 265
页数:5
相关论文
共 45 条
  • [1] Apoptosis induced in neuronal cells by oxidative stress: role played by caspases and intracellular calcium ions
    Annunziato, L
    Amoroso, S
    Pannaccione, A
    Cataldi, M
    Pignataro, G
    D'Alessio, A
    Sirabella, R
    Secondo, A
    Sibaud, L
    Di Renzo, GF
    [J]. TOXICOLOGY LETTERS, 2003, 139 (2-3) : 125 - 133
  • [2] Integration of endoplasmic reticulum signaling in health and disease
    Aridor, M
    Balch, WE
    [J]. NATURE MEDICINE, 1999, 5 (07) : 745 - 751
  • [3] Impairment of the ubiquitin-proteasome system by protein aggregation
    Bence, NF
    Sampat, RM
    Kopito, RR
    [J]. SCIENCE, 2001, 292 (5521) : 1552 - 1555
  • [4] Dissecting Fas signaling with an altered-specificity death-domain mutant: Requirement of FADD binding for apoptosis but not Jun N-terminal kinase activation
    Chang, HY
    Yang, XL
    Baltimore, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (04) : 1252 - 1256
  • [5] Activation of apoptosis signal regulating kinase 1 (ASK1) by the adapter protein Daxx
    Chang, HY
    Nishitoh, H
    Yang, XL
    Ichijo, H
    Baltimore, D
    [J]. SCIENCE, 1998, 281 (5384) : 1860 - 1863
  • [6] Persistent activation of c-Jun N-terminal kinase 1 (JNK1) in gamma radiation-induced apoptosis
    Chen, YR
    Meyer, CF
    Tan, TH
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (02) : 631 - 634
  • [7] ASK1 mediates apoptotic cell death induced by genotoxic stress
    Chen, ZH
    Seimiya, H
    Naito, M
    Mashima, T
    Kizaki, A
    Dan, S
    Imaizumi, M
    Ichijo, H
    Miyazono, K
    Tsuruo, T
    [J]. ONCOGENE, 1999, 18 (01) : 173 - 180
  • [8] Redox control of signal transduction, gene expression and cellular senescence
    Esposito, F
    Ammendola, R
    Faraonio, R
    Russo, T
    Cimino, F
    [J]. NEUROCHEMICAL RESEARCH, 2004, 29 (03) : 617 - 628
  • [9] Activation of apoptosis signal-regulating kinase 1 by reactive oxygen species through dephosphorylation at serine 967 and 14-3-3 dissociation
    Goldman, EH
    Chen, L
    Fu, H
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (11) : 10442 - 10449
  • [10] DIRECT EVIDENCE FOR TUMOR NECROSIS FACTOR-INDUCED MITOCHONDRIAL REACTIVE OXYGEN INTERMEDIATES AND THEIR INVOLVEMENT IN CYTOTOXICITY
    GOOSSENS, V
    GROOTEN, J
    DEVOS, K
    FIERS, W
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (18) : 8115 - 8119