Center for Neuroscience and Cell Biology (CNC), University of Coimbra, Coimbra, Portugal; Institute for Interdisciplinary Research, University of Coimbra, Coimbra, Portugal.
Center for Neuroscience and Cell Biology (CNC), University of Coimbra, Coimbra, Portugal.
Cell Rep. 2019 Jul 23;28(4):864-876.e6. doi: 10.1016/j.celrep.2019.06.080.
Ribosomes and a subset of cellular mRNAs are trafficked into axons of developing neurons. The axonal localization of translational machinery allows new proteins to be rapidly and locally synthesized during axonal growth and pathfinding. However, in mature neurons, axonal ribosomes are significantly reduced or even absent. The mechanism that elicits this removal is currently unknown. Here, we demonstrate that synapse formation is the trigger for ribosome reduction in mature axons. In vivo analysis shows that axonal ribosome levels decrease in rat brain at a developmental stage coincident with synapse formation. Next, we observe in vitro that different synaptogenic inducers trigger an overall decrease of ribosomal proteins and rRNA in the axons of spinal motor neurons. We further observe that this process is dependent on the ubiquitin-proteasome system but not on autophagy. Together, these data identify synaptogenesis as the long missing biological trigger that leads to ribosome disappearance during axonal maturation.
核糖体和细胞信使 RNA 的亚基被运送到发育中的神经元轴突中。翻译机制在轴突中的定位使新的蛋白质能够在轴突生长和寻径过程中快速且局部地合成。然而,在成熟的神经元中,轴突核糖体显著减少甚至缺失。引发这种去除的机制目前尚不清楚。在这里,我们证明了突触形成是成熟轴突中核糖体减少的触发因素。体内分析表明,在与突触形成一致的大鼠脑发育阶段,轴突核糖体水平降低。接下来,我们在体外观察到不同的突触发生诱导物触发脊髓运动神经元轴突中核糖体蛋白和 rRNA 的整体减少。我们进一步观察到,这个过程依赖于泛素蛋白酶体系统,但不依赖于自噬。总之,这些数据表明,突触发生是导致轴突成熟过程中核糖体消失的长期缺失的生物学触发因素。