Department of Neuroscience, Brown University Providence, RI, USA.
Front Neural Circuits. 2009 Nov 4;3:17. doi: 10.3389/neuro.04.017.2009. eCollection 2009.
The ability of the nervous system to convert transient experiences into long-lasting structural changes at the synapse relies upon protein synthesis. It has become increasingly clear that a critical subset of this synthesis occurs within the synaptic compartment. While this process has been extensively characterized in the postsynaptic compartment, the contribution of local translation to presynaptic function remains largely unexplored. However, recent evidence highlights the potential importance of translation within the presynaptic compartment. Work in cultured neurons has shown that presynaptic translation occurs specifically at synapses undergoing long-term plasticity and may contribute to the maintenance of nascent synapses. Studies from our laboratory have demonstrated that Fragile X proteins, which regulate mRNA localization and translation, are expressed at the presynaptic apparatus. Further, mRNAs encoding presynaptic proteins traffic into axons. Here we discuss recent advances in the study of presynaptic translation as well as the challenges confronting the field. Understanding the regulation of presynaptic function by local protein synthesis promises to shed new light on activity-dependent modification of synaptic architecture.
神经系统将短暂的体验转化为突触处的持久结构变化的能力依赖于蛋白质合成。越来越明显的是,这种合成的一个关键子集发生在突触间隙内。虽然这个过程在突触后区已经被广泛描述,但局部翻译对突触前功能的贡献在很大程度上仍未被探索。然而,最近的证据强调了翻译在突触前区的潜在重要性。在培养神经元中的研究表明,突触前翻译特异性地发生在经历长期可塑性的突触处,并可能有助于新形成的突触的维持。我们实验室的研究表明,调节 mRNA 定位和翻译的脆性 X 蛋白在突触前装置中表达。此外,编码突触前蛋白的 mRNAs 也在轴突中运输。在这里,我们讨论了突触前翻译研究的最新进展以及该领域面临的挑战。通过局部蛋白质合成来理解突触前功能的调节有望为活动依赖性突触结构修饰提供新的见解。