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首页> 外文期刊>Biochemical and Biophysical Research Communications >Real-time three-dimensional tracking of single synaptic vesicles reveals that synaptic vesicles undergoing kiss-and-run fusion remain close to their original fusion site before reuse
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Real-time three-dimensional tracking of single synaptic vesicles reveals that synaptic vesicles undergoing kiss-and-run fusion remain close to their original fusion site before reuse

机译:单个突触囊泡的实时三维跟踪显示,在重用之前,正在接受吻合融合的突触囊泡仍然靠近其原始融合现场。

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摘要

The release of neurotransmitters via the fusion between synaptic vesicles and the presynaptic membrane is an essential step in synaptic transmission. Synaptic vesicles generally undergo two distinct modes of exocytosis called full-collapse fusion and kiss-and-run fusion. In kiss-and-run fusion, the fusion pore of the synaptic vesicle opens transiently without the vesicle collapsing fully into the plasma membrane; thus, each synaptic vesicle can be used multiple times to release neurotransmitters. Despite considerable research, the detailed mechanisms that underlie kiss-and-run fusion remain elusive, particularly the location of synaptic vesicles after kiss-and-run events. To address this question, we performed real-time three-dimensional tracking of single synaptic vesicles labeled with a single quantum dot in the presynaptic terminal of cultured hippocampal neurons and analyzed the three-dimensional trajectories of these vesicles undergoing kiss-and-run fusion. We found that the majority of these synaptic vesicles underwent another exocytosis event within 120 nm of their original fusion site and underwent a second exocytosis event within 10 s of the first fusion event.
机译:通过突触囊泡和突触膜之间的融合释放神经递质是突触传递的基本步骤。突触囊泡通常经过两种不同的外毒性,称为全塌陷融合和亲吻和运行融合。在吻和运行融合中,突触囊泡的融合孔隙瞬时打开,没有囊泡完全塌陷到质膜中;因此,可以多次使用每个突触囊泡来释放神经递质。尽管研究相当大,但底层和运行融合的详细机制仍然难以难以捉摸,特别是吻斗事件后突触囊泡的位置。为了解决这个问题,我们对培养的海马神经元的突触前末端的单量子点标记的单个突触囊泡进行了实时三维跟踪,并分析了经历了吻和运行融合的这些囊泡的三维轨迹。我们发现,大多数这些突触囊泡在其原始融合位点的120 nm内接受了另一种外卵症事件,并在第一个融合事件的10秒内进行了第二个外毒性事件。

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