The fusion pore

被引:124
作者
Lindau, M [1 ]
de Toledo, GA
机构
[1] Cornell Univ, Sch Appl & Engn Phys, Ithaca, NY 14850 USA
[2] Univ Seville, Fac Med, Dept Fisiol Med & Biofis, E-41009 Seville, Spain
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2003年 / 1641卷 / 2-3期
关键词
membrane fusion; fusion pore; exocytosis; kiss-and-run; transmitter release;
D O I
10.1016/S0167-4889(03)00085-5
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 secretory process requires many different steps and stages. Vesicles must be formed and transported to the target membrane. They must be tethered or docked at the appropriate sites and must be prepared for fusion (priming). As the last step, a fusion pore is formed and the contents are released. Release of neurotransmitter is an extremely rapid event leading to rise times of the postsynaptic response of less than 100 mus. The release thus occurs during the initial formation of the exocytotic fusion pore. To understand the process of synaptic transmission, it is thus of outstanding importance to understand the molecular structure of the fusion pore, what are the properties of the initial fusion pore, how these properties affect the release process and what other factors may be limiting the kinetics of release. Here we review the techniques currently employed in fusion pore studies and discuss recent data and opinions on exocytotic fusion pore properties. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:167 / 173
页数:7
相关论文
共 71 条
[51]   BEGINNING OF EXOCYTOSIS CAPTURED BY RAPID-FREEZING OF LIMULUS AMEBOCYTES [J].
ORNBERG, RL ;
REESE, TS .
JOURNAL OF CELL BIOLOGY, 1981, 90 (01) :40-54
[52]   Trans-complex formation by proteolipid channels in the terminal phase of membrane fusion [J].
Peters, C ;
Bayer, MJ ;
Bühler, S ;
Andersen, JS ;
Mann, M ;
Mayer, A .
NATURE, 2001, 409 (6820) :581-588
[53]   Real-time measurements of vesicle-SNARE recycling in synapses of the central nervous system [J].
Sankaranarayanan, S ;
Ryan, TA .
NATURE CELL BIOLOGY, 2000, 2 (04) :197-204
[54]   Fusion pore expansion in horse eosinophils is modulated by Ca2+ and protein kinase C via distinct mechanisms [J].
Scepek, S ;
Coorssen, JR ;
Lindau, M .
EMBO JOURNAL, 1998, 17 (15) :4340-4345
[55]  
SCHMIDT W, 1983, EUR J CELL BIOL, V32, P31
[56]   Surface dynamics in living acinar cells imaged by atomic force microscopy: Identification of plasma membrane structures involved in exocytosis [J].
Schneider, SW ;
Sritharan, KC ;
Geibel, JP ;
Oberleithner, H ;
Jena, BP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (01) :316-321
[57]   PROPERTIES OF THE FUSION PORE THAT FORMS DURING EXOCYTOSIS OF A MAST-CELL SECRETORY VESICLE [J].
SPRUCE, AE ;
BRECKENRIDGE, LJ ;
LEE, AK ;
ALMERS, W .
NEURON, 1990, 4 (05) :643-654
[58]   Kiss and run exocytosis at hippocampal synapses [J].
Stevens, CF ;
Williams, JH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) :12828-12833
[59]  
Sulzer D, 2000, REV NEUROSCIENCE, V11, P159
[60]   Single and multiple vesicle fusion induce different rates of endocytosis at a central synapse [J].
Sun, JY ;
Wu, XS ;
Wu, LG .
NATURE, 2002, 417 (6888) :555-559