Fukaya Ryota, Miyano Rinako, Hirai Himawari, Sakaba Takeshi
Institute for Biology/Genetics, Freie Universität Berlin, Berlin, Germany.
Graduate School of Brain Science, Doshisha University, Kyoto, Japan.
Front Cell Neurosci. 2023 Jul 13;17:1237589. doi: 10.3389/fncel.2023.1237589. eCollection 2023.
Presynaptic plasticity is an activity-dependent change in the neurotransmitter release and plays a key role in dynamic modulation of synaptic strength. Particularly, presynaptic potentiation mediated by cyclic adenosine monophosphate (cAMP) is widely seen across the animals and thought to contribute to learning and memory. Hippocampal mossy fiber-CA3 pyramidal cell synapses have been used as a model because of robust presynaptic potentiation in short- and long-term forms. Moreover, direct presynaptic recordings from large mossy fiber terminals allow one to dissect the potentiation mechanisms. Recently, super-resolution microscopy and flash-and-freeze electron microscopy have revealed the localizations of release site molecules and synaptic vesicles during the potentiation at a nanoscale, identifying the molecular mechanisms of the potentiation. Incorporating these growing knowledges, we try to present plausible mechanisms underlying the cAMP-mediated presynaptic potentiation.
突触前可塑性是一种依赖于活动的神经递质释放变化,在突触强度的动态调节中起关键作用。特别是,由环磷酸腺苷(cAMP)介导的突触前增强在动物中广泛存在,并被认为有助于学习和记忆。海马苔藓纤维-CA3锥体细胞突触因其短期和长期形式的强大突触前增强作用而被用作模型。此外,从大型苔藓纤维终末进行的直接突触前记录使人们能够剖析增强机制。最近,超分辨率显微镜和闪光冷冻电子显微镜揭示了增强过程中释放位点分子和突触小泡在纳米尺度上的定位,确定了增强的分子机制。结合这些不断增长的知识,我们试图提出cAMP介导的突触前增强的合理机制。