Kaempf Natalie, Maritzen Tanja
Molecular Physiology and Cell Biology Section, Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Front Cell Neurosci. 2017 Oct 11;11:320. doi: 10.3389/fncel.2017.00320. eCollection 2017.
Communication between neurons relies on neurotransmitters which are released from synaptic vesicles (SVs) upon Ca stimuli. To efficiently load neurotransmitters, sense the rise in intracellular Ca and fuse with the presynaptic membrane, SVs need to be equipped with a stringently controlled set of transmembrane proteins. In fact, changes in SV protein composition quickly compromise neurotransmission and most prominently give rise to epileptic seizures. During exocytosis SVs fully collapse into the presynaptic membrane and consequently have to be replenished to sustain neurotransmission. Therefore, surface-stranded SV proteins have to be efficiently retrieved post-fusion to be used for the generation of a new set of fully functional SVs, a process in which dedicated endocytic sorting adaptors play a crucial role. The question of how the precise reformation of SVs is achieved is intimately linked to how SV membranes are retrieved. For a long time both processes were believed to be two sides of the same coin since Clathrin-mediated endocytosis (CME), the proposed predominant SV recycling mode, will jointly retrieve SV membranes and proteins. However, with the recent proposal of Clathrin-independent SV recycling pathways SV membrane retrieval and SV reformation turn into separable events. This review highlights the progress made in unraveling the molecular mechanisms mediating the high-fidelity retrieval of SV proteins and discusses how the gathered knowledge about SV protein recycling fits in with the new notions of SV membrane endocytosis.
神经元之间的通讯依赖于神经递质,神经递质在钙离子刺激下从突触小泡(SVs)中释放出来。为了有效地装载神经递质、感知细胞内钙离子的升高并与突触前膜融合,突触小泡需要配备一组严格控制的跨膜蛋白。事实上,突触小泡蛋白组成的变化会迅速损害神经传递,最显著的是引发癫痫发作。在胞吐过程中,突触小泡完全塌陷到突触前膜中,因此必须补充以维持神经传递。因此,表面滞留的突触小泡蛋白必须在融合后被有效地回收,以用于生成一组新的功能完全正常的突触小泡,在这个过程中,专门的内吞分选衔接蛋白起着至关重要的作用。突触小泡如何精确重塑的问题与突触小泡膜如何回收密切相关。长期以来,这两个过程都被认为是同一枚硬币的两面,因为网格蛋白介导的内吞作用(CME),即所提出的主要突触小泡回收模式,将共同回收突触小泡膜和蛋白。然而,随着最近提出的非网格蛋白依赖性突触小泡回收途径,突触小泡膜回收和突触小泡重塑变成了可分离的事件。这篇综述强调了在揭示介导突触小泡蛋白高保真回收的分子机制方面取得的进展,并讨论了关于突触小泡蛋白回收的现有知识如何与突触小泡膜内吞作用的新观念相契合。