BDNF signaling and survival of striatal neurons

被引:170
作者
Baydyuk, Maryna [1 ]
Xu, Baoji [2 ]
机构
[1] NINDS, NIH, Bethesda, MD 20892 USA
[2] Scripps Res Inst Florida, Dept Neurosci, Jupiter, FL 33458 USA
基金
美国国家卫生研究院;
关键词
neurotrophins; BDNF; TrkB; striatum; Huntington's disease; DRD1a; DRD2; dopaminergic neurons; HUNTINGTONS-DISEASE PHENOTYPES; NEUROTROPHIC FACTOR; MOUSE MODEL; SYNAPTIC PLASTICITY; PROJECTION NEURONS; PHOSPHATIDYLINOSITOL; 3-KINASE; STRIATOPALLIDAL NEURONS; POSTNATAL-DEVELOPMENT; RETROGRADE TRANSPORT; CELL-PROLIFERATION;
D O I
10.3389/fncel.2014.00254
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The striatum, a major component of the basal ganglia, performs multiple functions including control of movement, reward, and addiction. Dysfunction and death of striatal neurons are the main causes for the motor disorders associated with Huntington's disease (HD). Brain derived neurotrophic factor (BDNF), a member of the neurotrophin family, is among factors that promote survival and proper function of this neuronal population. Here, we review recent studies showing that BDNF determines the size of the striatum by supporting survival of the immature striatal neurons at their origin, promotes maturation of striatal neurons, and facilitates establishment of striatal connections during brain development. We also examine the role of BDNF in maintaining proper function of the striatum during adulthood, summarize the mechanisms that lead to a deficiency in BDNF signaling and subsequently striatal degeneration in HD, and highlight a potential role of BDNF as a therapeutic target for HD treatment.
引用
收藏
页数:10
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