Mechanisms of synaptic vesicle recycling illuminated by fluorescent dyes

被引:61
作者
Cousin, MA [1 ]
Robinson, PJ [1 ]
机构
[1] Childrens Med Res Inst, Cell Signalling Unit, Wentworthville, NSW 2145, Australia
关键词
exocytosis; endocytosis; synaptic vesicle; trafficking; FM1-43; nerve terminal;
D O I
10.1046/j.1471-4159.1999.0732227.x
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 recycling of synaptic vesicles in nerve terminals involves multiple steps, underlies all aspects of synaptic transmission, and is a key to understanding the basis of synaptic plasticity. The development of styryl dyes as fluorescent molecules that label recycling synaptic vesicles has revolutionized the way in which synaptic vesicle recycling can be investigated, by allowing an examination of processes in neurons that have long been inaccessible. In this review, we evaluate the major aspects of synaptic vesicle recycling that have been revealed and advanced by studies with styryl dyes, focussing upon synaptic vesicle fusion, retrieval, and trafficking. The greatest impact of styryl dyes has been to allow the routine visualization of endocytosis in central nerve terminals for the first time. This has revealed the kinetics of endocytosis, its underlying sequential steps, and its regulation by Ca2+. In studies of exocytosis, styryl dyes have helped distinguish between different modes of vesicle fusion, provided direct support for the quantal nature of exocytosis and endocytosis, and revealed how the probability of exocytosis varies enormously from one nerve terminal to another. Synaptic vesicle labelling with styryl dyes has helped our understanding of vesicle trafficking by allowing better under-standing of different synaptic vesicle pools within the nerve terminal, vesicle intermixing, and vesicle clustering at release sites. Finally, the dyes are now being used in innovative ways to reveal further insights into synaptic plasticity.
引用
收藏
页码:2227 / 2239
页数:13
相关论文
共 96 条
[1]   High calcium concentrations shift the mode of exocytosis to the kiss-and-run mechanism [J].
Alés, E ;
Tabares, L ;
Poyato, JM ;
Valero, V ;
Lindau, M ;
de Toledo, GA .
NATURE CELL BIOLOGY, 1999, 1 (01) :40-44
[2]   Monitoring secretion in real time: Capacitance, amperometry and fluorescence compared [J].
Angleson, JK ;
Betz, WJ .
TRENDS IN NEUROSCIENCES, 1997, 20 (07) :281-287
[3]   Calmodulin is the divalent cation receptor for rapid endocytosis, but not exocytosis, in adrenal chromaffin cells [J].
Artalejo, CR ;
Elhamdani, A ;
Palfrey, HC .
NEURON, 1996, 16 (01) :195-205
[4]   RAPID ENDOCYTOSIS COUPLED TO EXOCYTOSIS IN ADRENAL CHROMAFFIN CELLS INVOLVES CA2+, GTP, AND DYNAMIN BUT NOT CLATHRIN [J].
ARTALEJO, CR ;
HENLEY, JR ;
MCNIVEN, MA ;
PALFREY, CH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (18) :8328-8332
[5]   Amphiphysin I is associated with coated endocytic intermediates and undergoes stimulation-dependent dephosphorylation in nerve terminals [J].
Bauerfeind, R ;
Takei, K ;
De Camilli, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (49) :30984-30992
[6]   Imaging exocytosis and endocytosis [J].
Betz, WJ ;
Mao, F ;
Smith, CB .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (03) :365-371
[7]   OKADAIC ACID DISRUPTS CLUSTERS OF SYNAPTIC VESICLES IN FROG MOTOR-NERVE TERMINALS [J].
BETZ, WJ ;
HENKEL, AW .
JOURNAL OF CELL BIOLOGY, 1994, 124 (05) :843-854
[8]   OPTICAL ANALYSIS OF SYNAPTIC VESICLE RECYCLING AT THE FROG NEUROMUSCULAR-JUNCTION [J].
BETZ, WJ ;
BEWICK, GS .
SCIENCE, 1992, 255 (5041) :200-203
[9]   INTRACELLULAR MOVEMENTS OF FLUORESCENTLY LABELED SYNAPTIC VESICLES IN FROG MOTOR-NERVE TERMINALS DURING NERVE-STIMULATION [J].
BETZ, WJ ;
BEWICK, GS ;
RIDGE, RMAP .
NEURON, 1992, 9 (05) :805-813
[10]   The cysteine string secretory vesicle protein activates hsc70 ATPase [J].
Braun, JEA ;
Wilbanks, SM ;
Scheller, RH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (42) :25989-25993