Activation of a tyrosine kinase-MAPK cascade enhances the induction of long-term synaptic facilitation and long-term memory in Aplysia

被引:106
作者
Purcell, AL
Sharma, SK
Bagnall, MW
Sutton, MA
Carew, TJ [1 ]
机构
[1] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Ctr Neurobiol Learning & Memory, Irvine, CA 92697 USA
[3] Yale Univ, Interdepartmental Neurosci Program, New Haven, CT 06520 USA
[4] Univ Calif Irvine, Ctr Neurobiol Learning & Memory, Irvine, CA 92697 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0896-6273(03)00030-8
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Tyrosine kinases have been implicated in cellular processes thought to underlie learning and memory. Here we show that tyrosine kinases play a direct role in long-term synaptic facilitation (LTF) and long-term memory (LTM) for sensitization in Aplysia. Tyrosine kinase activity is required for serotonin-induced LTF of sensorimotor (SN-MN) synapses, and enhancement of endogenous tyrosine kinase activity facilitates the induction of LTF. These effects are mediated, at least in part, through mitogen-activated protein kinase (MAPK) activation and are blocked by transcriptional and translational inhibitors. Moreover, brain-derived neurotrophic factor (BDNF) also enhances the induction of LTF in a MAPK-dependent fashion. Finally, activation of endogenous tyrosine kinases enhances the induction of long-term memory for sensitization, and this enhancement also requires MAPK activation. Thus, tyrosine kinases, acting through MAPK, play a pivotal role in LTF and LTM formation.
引用
收藏
页码:473 / 484
页数:12
相关论文
共 56 条
[1]
AKIYAMA T, 1987, J BIOL CHEM, V262, P5592
[2]
Akiyama T., 1991, METHOD ENZYMOL, V201, P362
[3]
SPATIALLY RESOLVED DYNAMICS OF CAMP AND PROTEIN KINASE-A SUBUNITS IN APLYSIA SENSORY NEURONS [J].
BACSKAI, BJ ;
HOCHNER, B ;
MAHAUTSMITH, M ;
ADAMS, SR ;
KAANG, BK ;
KANDEL, ER ;
TSIEN, RY .
SCIENCE, 1993, 260 (5105) :222-226
[4]
STIMULATION OF PROTEIN TYROSINE PHOSPHORYLATION BY NMDA RECEPTOR ACTIVATION [J].
BADING, H ;
GREENBERG, ME .
SCIENCE, 1991, 253 (5022) :912-914
[5]
APLYSIA CREB2 REPRESSES LONG-TERM FACILITATION - RELIEF OF REPRESSION CONVERTS TRANSIENT FACILITATION INTO LONG-TERM FUNCTIONAL AND STRUCTURAL-CHANGE [J].
BARTSCH, D ;
GHIRARDI, M ;
SKEHEL, PA ;
KARL, KA ;
HERDER, SP ;
CHEN, M ;
BAILEY, CH ;
KANDEL, ER .
CELL, 1995, 83 (06) :979-992
[6]
CREB1 encodes a nuclear activator, a repressor, and a cytoplasmic modulator that form a regulatory unit critical for long-term facilitation [J].
Bartsch, D ;
Casadio, A ;
Karl, KA ;
Serodio, P ;
Kandel, ER .
CELL, 1998, 95 (02) :211-223
[7]
Peroxovanadium compounds: Biological actions and mechanism of insulin-mimesis [J].
Bevan, AP ;
Drake, PG ;
Yale, JF ;
Shaver, A ;
Posner, BI .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1995, 153 (1-2) :49-58
[8]
A signaling pathway to translational control [J].
Brown, EJ ;
Schreiber, SL .
CELL, 1996, 86 (04) :517-520
[9]
A transient, neuron-wide form of CREB-mediated long-term facilitation can be stabilized at specific synapses by local protein synthesis [J].
Casadio, A ;
Martin, KC ;
Giustetto, M ;
Zhu, HX ;
Chen, M ;
Bartsch, D ;
Bailey, CH ;
Kandel, ER .
CELL, 1999, 99 (02) :221-237
[10]
PRESYNAPTIC FACILITATION AS A MECHANISM FOR BEHAVIORAL SENSITIZATION IN APLYSIA [J].
CASTELLUCCI, V ;
KANDEL, ER .
SCIENCE, 1976, 194 (4270) :1176-1178