Multiple Roles for Frequenin/NCS-1 in Synaptic Function and Development

被引:37
|
作者
Dason, Jeffrey S. [1 ]
Romero-Pozuelo, Jesus [2 ]
Atwood, Harold L. [1 ]
Ferrus, Alberto [2 ]
机构
[1] Univ Toronto, Dept Physiol, Toronto, ON M5S 1A8, Canada
[2] CSIC, Inst Cajal, E-28002 Madrid, Spain
关键词
Neurotransmitter release; Calcium; Presynaptic; Postsynaptic; Facilitation; Short-term synaptic plasticity; LTP; Learning; Memory; Neurite outgrowth; Axon regeneration; Calcium-binding protein; Drosophila; NEURONAL CALCIUM SENSOR-1; PHOSPHATIDYLINOSITOL 4-KINASE ISOFORM; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR; ADRENAL CHROMAFFIN CELLS; ACCESSORY PROTEIN-LIKE; CA2+ BINDING-PROTEIN; IMMUNOCYTOCHEMICAL LOCALIZATION; NEUROMUSCULAR-JUNCTION; CONFORMATIONAL-CHANGES; CA2+-BINDING PROTEIN;
D O I
10.1007/s12035-012-8250-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The calcium-binding protein frequenin (Frq), discovered in the fruit fly Drosophila, and its mammalian homologue neuronal calcium sensor 1 (NCS-1) have been reported to affect several aspects of synaptic transmission, including basal levels of neurotransmission and short- and long-term synaptic plasticities. However, discrepant reports leave doubts about the functional roles of these conserved proteins. In this review, we attempt to resolve some of these seemingly contradictory reports. We discuss how stimulation protocols, sources of calcium (voltage-gated channels versus internal stores), and expression patterns (presynaptic versus postsynaptic) of Frq may result in the activation of various protein targets, leading to different synaptic effects. In addition, the potential interactions of Frq's C-terminal and N-terminal domains with other proteins are discussed. Frq also has a role in regulating neurite outgrowth, axonal regeneration, and synaptic development. We examine whether the effects of Frq on neurotransmitter release and neurite outgrowth are distinct or interrelated through homeostatic mechanisms. Learning and memory are affected by manipulations of Frq probably through changes in synaptic transmission and neurite outgrowth, raising the possibility that Frq may be implicated in human pathological conditions, including schizophrenia, bipolar disorder, and X-linked mental retardation.
引用
收藏
页码:388 / 402
页数:15
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