Neurodegenerative and physiological actions of c-Jun N-terminal kinases in the mammalian brain

被引:51
作者
Waetzig, V [1 ]
Herdegen, T [1 ]
机构
[1] Univ Klinikum Schleswig Holstein, Inst Pharmacol, D-24105 Kiel, Germany
关键词
AP-1; c-Jun; cytochrome c; cytoskeleton; microglia; signal transduction;
D O I
10.1016/j.neulet.2004.02.041
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The research in the field of AP-1 transcription factor expression, such as Jun or Fos proteins, in the brain was a milestone in neurosciences. The last years have provided growing insights into the upstream signal transduction which controls the expression and activation of these transcriptional regulators. In particular, the c-Jun N-terminal kinases (JNKs) were considered to confer degeneration by activation of c-Jun. Recent findings, however, demonstrate an essential physiological role of JNKs in the nervous system. Here we review the specific control and dual functions of JNK isoforms which are relevant for the development of the intact brain on the one hand, and which can confer dramatic neurodegenerative effects and microglial activation on the other hand. (C) 2004 Published by Elsevier Ireland Ltd.
引用
收藏
页码:64 / 67
页数:4
相关论文
共 50 条
  • [31] Essential roles of c-JUN and c-JUN N-terminal kinase (JNK) in neuregulin-increased expression of the acetylcholine receptor ε-subunit
    Si, JT
    Wang, Q
    Mei, L
    JOURNAL OF NEUROSCIENCE, 1999, 19 (19) : 8498 - 8508
  • [32] AP-1 mediated retinal photoreceptor apoptosis is independent of N-terminal phosphorylation of c-Jun
    Grimm, C
    Wenzel, A
    Behrens, A
    Hafezi, F
    Wagner, EF
    Remé, CE
    CELL DEATH AND DIFFERENTIATION, 2001, 8 (08) : 859 - 867
  • [33] AP-1 mediated retinal photoreceptor apoptosis is independent of N-terminal phosphorylation of c-Jun
    C Grimm
    A Wenzel
    A Behrens
    F Hafezi
    E F Wagner
    C E Remé
    Cell Death & Differentiation, 2001, 8 : 859 - 867
  • [34] Inhibition of c-Jun N-terminal kinase increases apoE expression in vitro and in vivo
    Pocivavsek, Ana
    Rebeck, G. William
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 387 (03) : 516 - 520
  • [35] Regulation of p73-mediated apoptosis by c-Jun N-terminal kinase
    Jones, Emma V.
    Dickman, Mark J.
    Whitmarsh, Alan J.
    BIOCHEMICAL JOURNAL, 2007, 405 (03) : 617 - 623
  • [36] Activation of c-Jun N-terminal kinase during ischemia and reperfusion in mouse liver
    Onishi, I
    Tani, T
    Hashimoto, T
    Shimizu, K
    Yagi, M
    Yamamoto, K
    Yoshioka, K
    FEBS LETTERS, 1997, 420 (2-3) : 201 - 204
  • [37] Endothelin promotes neurite elongation by a mechanism dependent on c-Jun N-terminal kinase
    Uesugi, Noriko
    Muramatsu, Rieko
    Yamashita, Toshihide
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 383 (04) : 509 - 512
  • [38] c-Jun N-Terminal Kinase Pathway Activation in Human and Experimental Cerebral Contusion
    Ortolano, Fabrizio
    Colombo, Alessio
    Zanier, Elisa Roncati
    Sclip, Allessandra
    Longhi, Luca
    Perego, Carlo
    Stocchetti, Nino
    Borsello, Tiziana
    De Simoni, Maria Grazia
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2009, 68 (09) : 964 - 971
  • [39] Neuroprotective properties of the C-Jun N-terminal kinase (JNK) inhibitor in hypoxic hypoxia
    Zyuz'kov, G. N.
    Udut, E., V
    Miroshnichenko, L. A.
    Poljakova, T. Ju
    Simanina, E., V
    Stavrova, L. A.
    Agafonov, V., I
    Zhdanov, V. V.
    BYULLETEN SIBIRSKOY MEDITSINY, 2019, 18 (02): : 80 - 88
  • [40] Induction of experimental autoimmune encephalomyelitis in the absence of c-Jun N-terminal kinase 2
    Nicolson, K
    Freland, S
    Weir, C
    Delahunt, B
    Flavell, RA
    Bäckström, BT
    INTERNATIONAL IMMUNOLOGY, 2002, 14 (08) : 849 - 856