Signalling for survival and death in neurones - The role of stress-activated kinases, JNK and p38

被引:268
作者
Harper, SJ
LoGrasso, P
机构
[1] Merck Sharp & Dohme Res Labs, Dept Pharmacol, Neurosci Res Ctr, Harlow CM20 2QR, Essex, England
[2] MRL San Diego, Dept Neuroinflammat, La Jolla, CA 92037 USA
关键词
JNK; p38; CEP1347; neurone; cell death; kinase;
D O I
10.1016/S0898-6568(01)00148-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The pathways involved in neuronal survival or death have been extensively studied mainly in cell lines. Recent evidence has suggested that activation of the stress activated pathways, jun N-terminal kinase (JNK) and p38 may play important roles in neuronal cell death or regeneration. In this review we will discuss these pathways in detail. We will examine the evidence that these pathways are important in neuronal cell death. Finally we will review the evidence that inhibitors of these pathways have a neuroprotective effect both in vitro and in vivo. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:299 / 310
页数:12
相关论文
共 153 条
  • [1] Deficiency of the stress kinase p38α results in embryonic lethality:: Characterization of the kinase dependence of stress responses of enzyme-deficient embryonic stem cells
    Allen, M
    Svensson, L
    Roach, M
    Hambor, J
    McNeish, J
    Gabel, CA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (05) : 859 - 869
  • [2] P53 is essential for developmental neuron death as regulated by the TrkA and p75 neurotrophin receptors
    Aloyz, RS
    Bamji, SX
    Pozniak, CD
    Toma, JG
    Atwal, J
    Kaplan, DR
    Miller, FD
    [J]. JOURNAL OF CELL BIOLOGY, 1998, 143 (06) : 1691 - 1703
  • [3] Anderson CNG, 1999, J NEUROSCI, V19, P664
  • [4] Anguelova E, 2000, J NEUROSCI RES, V59, P209, DOI 10.1002/(SICI)1097-4547(20000115)59:2<209::AID-JNR7>3.0.CO
  • [5] 2-I
  • [6] Inhibition of the cardiac p38-MAPK pathway by SB203580 delays ischemic cell death
    Barancik, M
    Htun, P
    Strohm, C
    Kilian, K
    Schaper, W
    [J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2000, 35 (03) : 474 - 483
  • [7] CEP-1347/KT7515, a JNK pathway inhibitor, supports the in vitro survival of chick embryonic neurons
    Borasio, GD
    Horstmann, S
    Anneser, JMH
    Neff, NT
    Glicksman, MA
    [J]. NEUROREPORT, 1998, 9 (07) : 1435 - 1439
  • [8] INVOLVEMENT OF RAS P21 IN NEUROTROPHIN-INDUCED RESPONSE OF SENSORY, BUT NOT SYMPATHETIC NEURONS
    BORASIO, GD
    MARKUS, A
    WITTINGHOFER, A
    BARDE, YA
    HEUMANN, R
    [J]. JOURNAL OF CELL BIOLOGY, 1993, 121 (03) : 665 - 672
  • [9] TRANSECTION OF RAT FIMBRIA-FORNIX INDUCES LASTING EXPRESSION OF C-JUN PROTEIN IN AXOTOMIZED SEPTAL NEURONS IMMUNONEGATIVE FOR CHOLINE-ACETYLTRANSFERASE AND NITRIC-OXIDE SYNTHASE
    BRECHT, S
    MARTINVILLALBA, A
    ZUSCHRATTER, W
    BRAVO, R
    HERDEGEN, T
    [J]. EXPERIMENTAL NEUROLOGY, 1995, 134 (01) : 112 - 125
  • [10] Medial septal cholinergic neurons express c-Jun but do not undergo DNA fragmentation after fornix-fimbria transections
    Butterworth, NJ
    Dragunow, M
    [J]. MOLECULAR BRAIN RESEARCH, 1996, 43 (1-2): : 1 - 12