NEUROTROPHIN-INDUCED MODULATION OF SYNAPTIC TRANSMISSION IN THE ADULT HIPPOCAMPUS

被引:100
作者
KANG, HJ
SCHUMAN, EM
机构
[1] Division of Biology 216-76, California Institute of Technology, Pasadena
关键词
NEUROTROPHIN; BDNF; NT-3; HIPPOCAMPUS; NEURONAL PLASTICITY;
D O I
10.1016/0928-4257(96)80547-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The NGF-family of neurotrophic factors including NGF, BDNF and NT-3,4/5 is known to be crucial for neuronal survival and differentiation during development. However, recent studies suggest that the neurotrophins are also widely expressed and play a dynamic role in the mature nervous system. One of the major sites of expression of the neurotrophins in the adult brain is the hippocampus which has been also popular as an important structure for the adult plasticity. Moreover, the level of expression of the neurotrophins in the hippocampus can be regulated by a variety of neuronal inputs, such as experimentally-induced seizures: injection of glutamate receptor agonists, and LTP-inducing stimulation. The possibility that the neurotrophins modulate synaptic transmission in the mature brain has been investigated at the Schaffer collateral-CA1 synapses in the adult rat hippocampus. We report that transient application of BDNF and NT-3, but not NGF induces a long-lasting increase of synaptic transmission, which is likely to be mediated by Trk family of receptor tyrosine kinases. Both BDNF and NT-3 decrease paired pulse facilitation, suggesting a possible presynaptic modification. interestingly, previous potentiation of synaptic activity by the application of neurotrophic factors does not occlode the induction of long-term potentiation. These results suggest that the neurotrophins may locally regulate synaptic plasticity in the adult nervous system.
引用
收藏
页码:11 / 22
页数:12
相关论文
共 57 条
[11]  
Elliott, Inturrisi, Black, Dreyfus, An improved method detects differential NGF and BDNF gene expression in response to depolarization in cultured hippocampal neurons, Mol Brain Res, 26, pp. 81-88, (1994)
[12]  
Ernfors, Wetmorc, Olson, Persson, Identification of cells in the rat brain and peripheral tissues expressing mRNA for members of the nerve growth factor family, Neuron, 5, pp. 511-526, (1990)
[13]  
Frey, Krug, Reymann, Matthies, Anisomycin, an inhibitor protein synthesis, blocks late phases of LTP phenomena in the hippocampal CA1 region in vitro, Brain Res, 452, pp. 57-65, (1988)
[14]  
Frey, Huang, Kandel, Effects of cAMP simulate a late stage of LTP in hippocampal CA1 neurons, Science, 260, pp. 1661-1664, (1993)
[15]  
Gwag, Springer, Activation of NMDA receptors increases BDNF mRNA expression in the hippocampal formation, Neuroreport, 5, pp. 125-128, (1993)
[16]  
Huang, Li, Kandel, cAMP contributes to mossy fiber LTP by initiating both a covalently mediated early phase and macromolecular synthesis-dependent late phase, Cell, 79, pp. 69-79, (1994)
[17]  
Holtzman, Li, Parada, Kinsman, Chen, Valletta, Zhou, Long, Mobley, p140trk mRNA marks NGF-responsive forebrain neurons: evidence that trk gene expression is induced by NGF, Neuron, 9, pp. 465-478, (1992)
[18]  
Ip, Ibanez, Nye, McClain, Jones, Gies, Belluscio, Le, Espinosa, Squinto, Persson, Yancopoulos, Mammalian neurotrophin-4: structure, chromosomal localization, tissue distribution, and receptor specificity, Proc Natl Acad Sci USA, 89, pp. 3060-3064, (1992)
[19]  
Ip, Li, Yancopoulos, Lindsay, Cultured hippocampal neurons show responses to BDNF, NT-3, and NT-4, but not NGF, J Neurosci, 13, pp. 3394-3405, (1993)
[20]  
Isackson, Huntsman, Murray, Gall, BDNF mRNA expression is increased in the adult rat forebrain after limbic seizures: temporal patterns of induction distinct from NGF, Neuron, 6, pp. 937-948, (1991)