Presynaptic dysfunction in neurodevelopmental disorders: Insights from the synaptic vesicle life cycle

被引:53
作者
Bonnycastle, Katherine [1 ,2 ,3 ]
Davenport, Elizabeth C. [1 ,2 ,3 ]
Cousin, Michael A. [1 ,2 ,3 ]
机构
[1] Univ Edinburgh, Ctr Discovery Brain Sci, Hugh Robson Bldg,George Sq, Edinburgh EH8 9XD, Midlothian, Scotland
[2] Univ Edinburgh, Muir Maxwell Epilepsy Ctr, Edinburgh, Midlothian, Scotland
[3] Univ Edinburgh, Simons Initiat Dev Brain, Edinburgh, Midlothian, Scotland
基金
英国惠康基金; 芬兰科学院;
关键词
autism; endocytosis; epilepsy; exocytosis; intellectual disability; neurotransmission; vesicle; DE-NOVO MUTATIONS; DEPENDENT BULK ENDOCYTOSIS; OF-FUNCTION MUTATIONS; FRAGILE-X-SYNDROME; PAROXYSMAL KINESIGENIC DYSKINESIA; CLATHRIN-MEDIATED ENDOCYTOSIS; DANDY-WALKER MALFORMATION; AUTISM SPECTRUM DISORDER; BASAL GANGLIA DISEASE; SHORT-TERM PLASTICITY;
D O I
10.1111/jnc.15035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The activity-dependent fusion, retrieval and recycling of synaptic vesicles is essential for the maintenance of neurotransmission. Until relatively recently it was believed that most mutations in genes that were essential for this process would be incompatible with life, because of this fundamental role. However, an ever-expanding number of mutations in this very cohort of genes are being identified in individuals with neurodevelopmental disorders, including autism, intellectual disability and epilepsy. This article will summarize the current state of knowledge linking mutations in presynaptic genes to neurodevelopmental disorders by sequentially covering the various stages of the synaptic vesicle life cycle. It will also discuss how perturbations of specific stages within this recycling process could translate into human disease. Finally, it will also provide perspectives on the potential for future therapy that are targeted to presynaptic function.
引用
收藏
页码:179 / 207
页数:29
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