Leibniz Group "Dendritic Organelles and Synaptic Function", Center for Molecular Neurobiology, ZMNH, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Research Group Neuroplasticity, Leibniz Institute for Neurobiology, Magdeburg, Germany.
EMBO J. 2022 Apr 4;41(7):e110057. doi: 10.15252/embj.2021110057. Epub 2022 Mar 14.
Synaptic function crucially relies on the constant supply and removal of neuronal membranes. The morphological complexity of neurons poses a significant challenge for neuronal protein transport since the machineries for protein synthesis and degradation are mainly localized in the cell soma. In response to this unique challenge, local micro-secretory systems have evolved that are adapted to the requirements of neuronal membrane protein proteostasis. However, our knowledge of how neuronal proteins are synthesized, trafficked to membranes, and eventually replaced and degraded remains scarce. Here, we review recent insights into membrane trafficking at synaptic sites and into the contribution of local organelles and micro-secretory pathways to synaptic function. We describe the role of endoplasmic reticulum specializations in neurons, Golgi-related organelles, and protein complexes like retromer in the synthesis and trafficking of synaptic transmembrane proteins. We discuss the contribution of autophagy and of proteasome-mediated and endo-lysosomal degradation to presynaptic proteostasis and synaptic function, as well as nondegradative roles of autophagosomes and lysosomes in signaling and synapse remodeling. We conclude that the complexity of neuronal cyto-architecture necessitates long-distance protein transport that combines degradation with signaling functions.
突触功能严重依赖于神经元膜的持续供应和去除。神经元的形态复杂性对神经元蛋白运输构成了重大挑战,因为蛋白质合成和降解的机制主要定位于细胞体。为了应对这一独特的挑战,已经进化出了局部微分泌系统,以适应神经元膜蛋白稳态的要求。然而,我们对神经元蛋白如何合成、运输到膜上,以及最终被替换和降解的了解仍然很少。在这里,我们回顾了最近关于突触部位膜运输以及局部细胞器和微分泌途径对突触功能贡献的研究进展。我们描述了内质网特化在神经元中的作用、高尔基体相关细胞器以及逆行蛋白复合物(retromer)在突触跨膜蛋白的合成和运输中的作用。我们讨论了自噬以及蛋白酶体介导的和内体溶酶体降解对突触前蛋白稳态和突触功能的贡献,以及自噬体和溶酶体在信号转导和突触重塑中的非降解作用。我们得出结论,神经元细胞结构的复杂性需要长距离蛋白运输,这种运输将降解与信号功能结合起来。