Laboratory of Molecular Basis of Synaptic Plasticity, Centre of New Technologies, University of Warsaw, Warsaw, Poland.
Institute of Biochemistry and Biophysics, PAS, Warsaw, Poland.
EMBO Rep. 2020 Aug 5;21(8):e48882. doi: 10.15252/embr.201948882. Epub 2020 Jun 18.
Synapses are the regions of the neuron that enable the transmission and propagation of action potentials on the cost of high energy consumption and elevated demand for mitochondrial ATP production. The rapid changes in local energetic requirements at dendritic spines imply the role of mitochondria in the maintenance of their homeostasis. Using global proteomic analysis supported with complementary experimental approaches, we show that an essential pool of mitochondrial proteins is locally produced at the synapse indicating that mitochondrial protein biogenesis takes place locally to maintain functional mitochondria in axons and dendrites. Furthermore, we show that stimulation of synaptoneurosomes induces the local synthesis of mitochondrial proteins that are transported to the mitochondria and incorporated into the protein supercomplexes of the respiratory chain. Importantly, in a mouse model of fragile X syndrome, Fmr1 KO mice, a common disease associated with dysregulation of synaptic protein synthesis, we observed altered morphology and respiration rates of synaptic mitochondria. That indicates that the local production of mitochondrial proteins plays an essential role in synaptic functions.
突触是神经元的区域,通过消耗大量能量和提高对线粒体 ATP 生成的需求,实现动作电位的传递和传播。树突棘局部能量需求的快速变化意味着线粒体在维持其稳态中的作用。我们使用支持互补实验方法的全局蛋白质组学分析表明,线粒体蛋白的必需池在突触处局部产生,表明线粒体蛋白生物发生发生在局部,以维持轴突和树突中功能性线粒体。此外,我们还表明,刺激突触小体诱导线粒体蛋白的局部合成,这些蛋白被转运到线粒体并整合到呼吸链的蛋白质超级复合物中。重要的是,在脆性 X 综合征的小鼠模型中,Fmr1 KO 小鼠,一种与突触蛋白合成失调相关的常见疾病,我们观察到突触线粒体的形态和呼吸速率发生改变。这表明线粒体蛋白的局部产生在突触功能中起着至关重要的作用。