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摘要:
Brain-derived neurotrophic factor (BDNF) is a neurotrophin that elicits neuronal survival and differentiation, synaptic transmission, and the modulation of synaptic plasticity. The biological actions of BDNF are mediated via two distinct receptors: the high-affinity tropomyosin-related kinase B (TrkB) receptor and the low-affinity p75 neurotrophin receptor (p75NTR). Recent findings regarding the actions and mechanisms of BDNF are reviewed here. Activity-dependent synaptic plasticity, as exemplified by long-term potentiation (LTP) and long-term depression (LTD), underlies the cellular mechanism of learning and memory. An accumulating body of evidence shows that BDNF modulates synaptic plasticity. This function requires extracellular neurotrophin release, synaptic activity-dependent local protein synthesis. In addition, a precursor of BDNF, proBDNF, is emerging as a new ligand with biological activities that are distinct from those of BDNF. The proteolytic cleavage of proBDNF is also proposed as a mechanism that determines the direction of BDNF actions. This review discusses the post-translational processing of proBDNF, the modulatory roles of the human BDNF polymorphism Val66Met, recent reports of the novel mechanisms of BDNF expression, and clinical reports showing the roles of BDNF in the blood. Taken together, these data provide new insights into the biological roles of BDNF and its related molecules in the central nervous system.
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篇名 The Biological Actions and Mechanisms of Brain-Derived Neurotrophic Factor in Healthy and Disordered Brains
来源期刊 神经系统科学与医药(英文) 学科 医学
关键词 Component BRAIN-DERIVED NEUROTROPHIC Factor (BDNF) Tropomyosin-Related Kinase B (TrkB) Synaptic Plasticity Polymorphism PROTEOLYTIC Cleavage
年,卷(期) 2014,(4) 所属期刊栏目
研究方向 页码范围 183-195
页数 13页 分类号 R73
字数 语种
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Component
BRAIN-DERIVED
NEUROTROPHIC
Factor
(BDNF)
Tropomyosin-Related
Kinase
B
(TrkB)
Synaptic
Plasticity
Polymorphism
PROTEOLYTIC
Cleavage
研究起点
研究来源
研究分支
研究去脉
引文网络交叉学科
相关学者/机构
期刊影响力
神经系统科学与医药(英文)
季刊
2158-2912
武汉市江夏区汤逊湖北路38号光谷总部空间
出版文献量(篇)
287
总下载数(次)
0
总被引数(次)
0
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