The synapsins: Key actors of synapse function and plasticity

被引:474
作者
Cesca, F. [1 ]
Baldelli, P. [1 ,2 ,3 ]
Valtorta, F. [4 ,5 ]
Benfenati, F. [1 ,2 ,3 ]
机构
[1] Italian Inst Technol, Dept Neurosci & Brain Technol, I-16163 Genoa, Italy
[2] Univ Genoa, Dept Expt Med, I-16132 Genoa, Italy
[3] Ist Nazl Neurosci, I-16132 Genoa, Italy
[4] Univ Vita Salute San Raffaele, San Raffaele Sci Inst, I-20132 Milan, Italy
[5] IIT Unit Mol Neurosci, I-20132 Milan, Italy
关键词
Synaptic vesicles; Actin cytoskeleton; Synaptic transmission; Synaptic plasticity; Epilepsy; PROTEIN-KINASE-II; LONG-TERM POTENTIATION; L-ISOASPARTYL METHYLTRANSFERASE; SEROTONIN STIMULATES PHOSPHORYLATION; NEURON-SPECIFIC PHOSPHOPROTEIN; SITE-SPECIFIC PHOSPHORYLATION; READILY RELEASABLE POOL; ATOMIC-FORCE MICROSCOPE; RAB3 EFFECTOR PROTEIN; SODIUM-CHANNEL GENE;
D O I
10.1016/j.pneurobio.2010.04.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The synapsins are a family of neuronal phosphoproteins evolutionarily conserved in invertebrate and vertebrate organisms. Their best-characterised function is to modulate neurotransmitter release at the pre-synaptic terminal, by reversibly tethering synaptic vesicles (SVs) to the actin cytoskeleton. However, many recent data have suggested novel functions for synapsins in other aspects of the pre-synaptic physiology, such as SV docking, fusion and recycling. Synapsin activity is tightly regulated by several protein kinases and phosphatases, which modulate the association of synapsins to SVs as well as their interaction with actin filaments and other synaptic proteins. In this context, synapsins act as a link between extracellular stimuli and the intracellular signalling events activated upon neuronal stimulation. Genetic manipulation of synapsins in various in vivo models has revealed that, although not essential for the basic development and functioning of neuronal networks, these proteins are extremely important in the fine-tuning of neuronal plasticity, as shown by the epileptic phenotype and behavioural abnormalities characterising mouse lines lacking one or more synapsin isoforms. In this review, we summarise the current knowledge about how the various members of the synapsin family are involved in the modulation of the pre-synaptic physiology. We give a comprehensive description of the molecular basis of synapsin function, as well as an overview of the more recent evidence linking mutations in the synapsin proteins to the onset of severe central nervous system diseases such as epilepsy and schizophrenia. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:313 / 348
页数:36
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