Three-dimensional architecture of presynaptic terminal cytomatrix

被引:232
作者
Siksou, Lea
Rostaing, Philippe
Lechaire, Jean-Pierre
Boudier, Thomas
Ohtsuka, Toshihisa
Fejtova, Anna
Kao, Hung-Teh
Greengard, Paul
Gundelfinger, Eckart D.
Triller, Antoine
Marty, Serge
机构
[1] INSERM, Ecole Normale Super, U789, F-75005 Paris, France
[2] Univ Paris 06, CNRS, Serv CryoMicroscopie Elect, Inst Federat Rech Biol Integrat 83, F-75252 Paris 05, France
[3] Ctr Univ Orsay, INSERM, U759, Inst Curie, F-91405 Orsay, France
[4] Toyama Med & Pharmaceut Univ, Fac Med, Dept Clin & Mol Pathol, Grad Sch Med, Sugitani, Toyama 9300194, Japan
[5] Leibniz Inst Neurobiol, Dept Neurochem & Mol Biol, D-39118 Magdeburg, Germany
[6] NYU, Sch Med, Dept Psychiat, Orangeburg, NY 10962 USA
[7] Nathan S Kline Inst Psychiat Res, Orangeburg, NY 10962 USA
[8] Rockefeller Univ, New York, NY 10021 USA
关键词
hippocampus; synapsin; synaptic vesicles; active zone; electron tomography; high-pressure freezing;
D O I
10.1523/JNEUROSCI.1773-07.2007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Presynaptic terminals are specialized for mediating rapid fusion of synaptic vesicles (SVs) after calcium influx. The regulated trafficking of SVs likely results from a highly organized cytomatrix. How this cytomatrix links SVs, maintains them near the active zones (AZs) of release, and organizes docked SVs at the release sites is not fully understood. To analyze the three-dimensional (3D) architecture of the presynaptic cytomatrix, electron tomography of presynaptic terminals contacting spines was performed in the stratum radiatum of the rat hippocampal CA1 area. To preserve the cytomatrix, hippocampal slices were immobilized using high-pressure freezing, followed by cryosubstitution and embedding. SVs are surrounded by a dense network of filaments. A given vesicle is connected to similar to 1.5 neighboring ones. SVs at the periphery of this network are also linked to the plasma membrane, by longer filaments. More of these filaments are found at the AZ. At the AZ, docked SVs are grouped around presynaptic densities. Filaments with adjacent SVs emerge from these densities. Immunogold localizations revealed that synapsin is located in the presynaptic bouton, whereas Bassoon and CAST( ERC2) are at focal points next to the AZ. In synapsin triple knock-out mice, the number of SVs is reduced by 63%, but the size of the boutons is reduced by only 18%, and the mean distance of SVs to the AZ is unchanged. This 3D analysis reveals the morphological constraints exerted by the presynaptic molecular scaffold. SVs are tightly interconnected in the axonal bouton, and this network is preferentially connected to the AZ.
引用
收藏
页码:6868 / 6877
页数:10
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