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Munc13-1对于谷氨酸能突触小泡的融合能力至关重要。

Munc13-1 is essential for fusion competence of glutamatergic synaptic vesicles.

作者信息

Augustin I, Rosenmund C, Südhof T C, Brose N

机构信息

Max-Planck-Institut für Experimentelle Medizin, AG Molekulare Neurobiologie, Göttingen, Bundesrepublik Deutschland.

出版信息

Nature. 1999 Jul 29;400(6743):457-61. doi: 10.1038/22768.

Abstract

Neurotransmitter release at synapses between nerve cells is mediated by calcium-triggered exocytotic fusion of synaptic vesicles. Before fusion, vesicles dock at the presynaptic release site where they mature to a fusion-competent state. Here we identify Munc13-1, a brain-specific presynaptic phorbol ester receptor, as an essential protein for synaptic vesicle maturation. We show that glutamatergic hippocampal neurons from mice lacking Munc13-1 form ultrastructurally normal synapses whose synaptic-vesicle cycle is arrested at the maturation step. Transmitter release from mutant synapses cannot be triggered by action potentials, calcium-ionophores or hypertonic sucrose solution. In contrast, release evoked by alpha-latrotoxin is indistinguishable from wild-type controls, indicating that the toxin can bypass Munc13-1-mediated vesicle maturation. A small subpopulation of synapses of any given glutamatergic neuron as well as all synapses of GABA (gamma-aminobutyric acid)-containing neurons are unaffected by Munc13-1 loss, demonstrating the existence of multiple and transmitter-specific synaptic vesicle maturation processes in synapses.

摘要

神经细胞之间突触处的神经递质释放是由钙触发的突触小泡胞吐融合介导的。在融合之前,小泡停靠在突触前释放位点,在那里它们成熟到具备融合能力的状态。在这里,我们确定Munc13-1,一种脑特异性突触前佛波酯受体,是突触小泡成熟的必需蛋白。我们发现,来自缺乏Munc13-1的小鼠的谷氨酸能海马神经元形成了超微结构正常的突触,其突触小泡循环在成熟步骤被阻断。突变突触的递质释放不能由动作电位、钙离子载体或高渗蔗糖溶液触发。相比之下,α-银环蛇毒素诱发的释放与野生型对照无差异,表明该毒素可以绕过Munc13-1介导的小泡成熟过程。任何给定谷氨酸能神经元的一小部分突触以及所有含γ-氨基丁酸(GABA)神经元的突触不受Munc13-1缺失的影响,这表明突触中存在多种递质特异性的突触小泡成熟过程。

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