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在海兔的同源突触增强开始时,突触素簇迅速增加。

Rapid increase in clusters of synaptophysin at onset of homosynaptic potentiation in Aplysia.

机构信息

Department of Neuroscience, Columbia University, New York, NY 10032, USA.

出版信息

Proc Natl Acad Sci U S A. 2011 Jul 12;108(28):11656-61. doi: 10.1073/pnas.1102695108. Epub 2011 Jun 27.

Abstract

Imaging studies have shown that even the earliest phases of long-term plasticity are accompanied by the rapid recruitment of synaptic components, which generally requires actin polymerization and may be one of the first steps in a program that can lead to the formation of new stable synapses during late-phase plasticity. However, most of those results come from studies of long-term potentiation in rodent hippocampus and might not generalize to other forms of synaptic plasticity or plasticity in other brain areas and species. For example, recruitment of presynaptic proteins during long-term facilitation by 5HT in Aplysia is delayed for several hours, suggesting that whereas activity-dependent forms of plasticity, such as long-term potentiation, involve rapid recruitment of presynaptic proteins, neuromodulatory forms of plasticity, such as facilitation by 5HT, involve more delayed recruitment. To begin to explore this hypothesis, we examined an activity-dependent form of plasticity, homosynaptic potentiation produced by tetanic stimulation of the presynaptic neuron in Aplysia. We found that homosynaptic potentiation involves presynaptic but not postsynaptic actin and a rapid (under 10 min) increase in the number of clusters of the presynaptic vesicle-associated protein synaptophysin. These results indicate that rapid recruitment of synaptic components is not limited to hippocampal potentiation and support the hypothesis that activity-dependent types of plasticity involve rapid recruitment of presynaptic proteins, whereas neuromodulatory types of plasticity involve more delayed recruitment.

摘要

影像学研究表明,即使是长期可塑性的早期阶段也伴随着突触成分的快速募集,这通常需要肌动蛋白聚合,并且可能是导致晚期可塑性中新的稳定突触形成的程序的第一步。然而,这些结果大多来自于对啮齿动物海马体的长时程增强的研究,可能不适用于其他形式的突触可塑性或其他脑区和物种的可塑性。例如,在海兔中,5-HT 诱导的长时程易化过程中,突触前蛋白的募集延迟了几个小时,这表明,虽然依赖于活动的形式的可塑性,如长时程增强,涉及突触前蛋白的快速募集,但神经调质形式的可塑性,如 5-HT 诱导的易化,则涉及更延迟的募集。为了开始探索这一假说,我们研究了一种依赖于活动的可塑性形式,即在海兔中通过刺激突触前神经元的强直刺激产生的同源突触增强。我们发现,同源突触增强涉及突触前但不涉及突触后肌动蛋白,以及突触小泡相关蛋白突触素簇数量的快速(在 10 分钟内)增加。这些结果表明,突触成分的快速募集不仅限于海马体的增强,并且支持这样的假说,即依赖于活动的类型的可塑性涉及突触前蛋白的快速募集,而神经调质类型的可塑性涉及更延迟的募集。

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