Selective engagement of plasticity mechanisms for motor memory storage

被引:111
作者
Boyden, Edward S.
Katoh, Akira
Pyle, Jason L.
Chatila, Tallal A.
Tsien, Richard W.
Raymond, Jennifer L. [1 ]
机构
[1] Stanford Univ, Dept Neurobiol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
[3] Univ Calif Los Angeles, Dept Pediat, David Geffen Sch Med, Los Angeles, CA USA
关键词
LONG-TERM DEPRESSION; CA2+/CALMODULIN-DEPENDENT PROTEIN-KINASE; VESTIBULO-OCULAR REFLEX; CEREBELLAR PURKINJE-CELLS; PURSUIT EYE-MOVEMENTS; RAT CEREBELLUM; NITRIC-OXIDE; MUTANT MICE; LATE-PHASE; DYNAMIC CHARACTERISTICS;
D O I
10.1016/j.neuron.2006.08.026
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The number and diversity of plasticity mechanisms in the brain raises a central question: does a neural circuit store all memories by stereotyped application of the available plasticity mechanisms, or can subsets of these mechanisms be selectively engaged for specific memories? The uniform architecture of the cerebellum has inspired the idea that plasticity mechanisms like cerebellar long-term depression (LTD) contribute universally to memory storage. To test this idea, we investigated a set of closely related, cerebellum-dependent motor memories. In mutant mice lacking Ca2+/calmodulin-dependent protein kinase IV (CaMKIV), the maintenance of cerebellar LTD is abolished. Although memory for an increase in the gain of the vestibulo-ocular reflex (VOR) induced with high-frequency stimuli was impaired in these mice, memories for decreases in VOR gain and increases in gain induced with low-frequency stimuli were intact. Thus, a particular plasticity mechanism need not support all cerebellum-dependent memories, but can be engaged selectively according to the parameters of training.
引用
收藏
页码:823 / 834
页数:12
相关论文
共 83 条
[1]   Genetic demonstration of a role for PKA in the late phase of LTP and in hippocampus-based long-term memory [J].
Abel, T ;
Nguyen, PV ;
Barad, M ;
Deuel, TAS ;
Kandel, ER .
CELL, 1997, 88 (05) :615-626
[2]   A late phase of cerebellar long-term depression requires activation of CaMKIV and CREB [J].
Ahn, S ;
Ginty, DD ;
Linden, DJ .
NEURON, 1999, 23 (03) :559-568
[3]   REDUCED HIPPOCAMPAL LONG-TERM POTENTIATION AND CONTEXT-SPECIFIC DEFICIT IN ASSOCIATIVE LEARNING IN MGLUR1 MUTANT MICE [J].
AIBA, A ;
CHEN, C ;
HERRUP, K ;
ROSENMUND, C ;
STEVENS, CF ;
TONEGAWA, S .
CELL, 1994, 79 (02) :365-375
[4]  
ALBUS J S, 1971, Mathematical Biosciences, V10, P25, DOI 10.1016/0025-5564(71)90051-4
[5]   Regulation and function of the calcium/calmodulin-dependent protein kinase IV/protein serine/threonine phosphatase 2A signaling complex [J].
Anderson, KA ;
Noeldner, PK ;
Reece, K ;
Wadzinski, BE ;
Means, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (30) :31708-31716
[6]   Long-term potentiation of intrinsic excitability at the Mossy fiber-granule cell synapse of rat cerebellum [J].
Armano, S ;
Rossi, P ;
Taglietti, V ;
D'Angelo, E .
JOURNAL OF NEUROSCIENCE, 2000, 20 (14) :5208-5216
[7]   Zonal organization of flocculo-vestibular connections in rats [J].
Balaban, CD ;
Schuerger, RJ ;
Porter, JD .
NEUROSCIENCE, 2000, 99 (04) :669-682
[8]   IMPAIRMENT OF SPATIAL BUT NOT CONTEXTUAL MEMORY IN CAMKII MUTANT MICE WITH A SELECTIVE LOSS OF HIPPOCAMPAL LTP IN THE RANGE OF THE THETA-FREQUENCY [J].
BEACH, ME ;
HAWKINS, RD ;
OSMAN, M ;
KANDEL, ER ;
MAYFORD, M .
CELL, 1995, 81 (06) :905-915
[9]   Regional and cellular distribution of neural visinin-like protein immunoreactivities (VILIP-1 and VILIP-3) in human brain [J].
Bernstein, HG ;
Baumann, B ;
Danos, P ;
Diekmann, S ;
Bogerts, B ;
Gundelfinger, ED ;
Braunewell, KH .
JOURNAL OF NEUROCYTOLOGY, 1999, 28 (08) :655-662
[10]   CREB phosphorylation and dephosphorylation: A Ca2(+)- and stimulus duration-dependent switch for hippocampal gene expression [J].
Bito, H ;
Deisseroth, K ;
Tsien, RW .
CELL, 1996, 87 (07) :1203-1214