Bellouze Sarah, Schäfer Michael K, Buttigieg Dorothée, Baillat Gilbert, Rabouille Catherine, Haase Georg
Institut de Neurosciences de la Timone, Centre National de la Recherche Scientifique (CNRS) and Aix-Marseille Université UMR7289, Marseille, France.
Klinik für Anästhesiologie, Universitätsmedizin Mainz, Mainz, Germany.
Hum Mol Genet. 2014 Nov 15;23(22):5961-75. doi: 10.1093/hmg/ddu320. Epub 2014 Jun 20.
Golgi fragmentation is an early hallmark of many neurodegenerative diseases but its pathophysiological relevance and molecular mechanisms are unclear. We here demonstrate severe and progressive Golgi fragmentation in motor neurons of progressive motor neuronopathy (pmn) mice due to loss of the Golgi-localized tubulin-binding cofactor E (TBCE). Loss of TBCE in mutant pmn and TBCE-depleted motor neuron cultures causes defects in Golgi-derived microtubules, as expected, but surprisingly also reduced levels of COPI subunits, decreased recruitment of tethering factors p115/GM130 and impaired Golgi SNARE-mediated vesicle fusion. Conversely, ARF1, which stimulates COPI vesicle formation, enhances the recruitment of TBCE to the Golgi, increases polymerization of Golgi-derived microtubules and rescues TBCE-linked Golgi fragmentation. These data indicate an ARF1/TBCE-mediated cross-talk that coordinates COPI formation and tubulin polymerization at the Golgi. We conclude that interruption of this cross-talk causes Golgi fragmentation in pmn mice and hypothesize that similar mechanisms operate in human amyotrophic lateral sclerosis and spinal muscular atrophy.
高尔基体碎片化是许多神经退行性疾病的早期特征,但其病理生理相关性和分子机制尚不清楚。我们在此证明,由于高尔基体定位的微管蛋白结合辅因子E(TBCE)缺失,进行性运动神经元病(pmn)小鼠的运动神经元中出现严重且进行性的高尔基体碎片化。正如预期的那样,突变型pmn小鼠和TBCE缺失的运动神经元培养物中TBCE的缺失导致高尔基体衍生微管出现缺陷,但令人惊讶的是,这也降低了COPI亚基的水平,减少了拴系因子p115/GM130的募集,并损害了高尔基体SNARE介导的囊泡融合。相反,刺激COPI囊泡形成的ARF1增强了TBCE向高尔基体的募集,增加了高尔基体衍生微管的聚合,并挽救了与TBCE相关的高尔基体碎片化。这些数据表明存在一种ARF1/TBCE介导的相互作用,可在高尔基体协调COPI形成和微管蛋白聚合。我们得出结论,这种相互作用的中断导致pmn小鼠的高尔基体碎片化,并推测类似机制在人类肌萎缩侧索硬化症和脊髓性肌萎缩症中起作用。