Schaefer Michael K E, Schmalbruch Henning, Buhler Emmanuelle, Lopez Catherine, Martin Natalia, Guénet Jean-Louis, Haase Georg
Inserm, Unité 29, Equipe Avenir, Marseille, France.
J Neurosci. 2007 Aug 15;27(33):8779-89. doi: 10.1523/JNEUROSCI.1599-07.2007.
Axonal degeneration represents one of the earliest pathological features in motor neuron diseases. We here studied the underlying molecular mechanisms in progressive motor neuronopathy (pmn) mice mutated in the tubulin-specific chaperone TBCE. We demonstrate that TBCE is a peripheral membrane-associated protein that accumulates at the Golgi apparatus. In pmn mice, TBCE is destabilized and disappears from the Golgi apparatus of motor neurons, and microtubules are lost in distal axons. The axonal microtubule loss proceeds retrogradely in parallel with the axonal dying back process. These degenerative changes are inhibited in a dose-dependent manner by transgenic TBCE complementation that restores TBCE expression at the Golgi apparatus. In cultured motor neurons, the pmn mutation, interference RNA-mediated TBCE depletion, and brefeldin A-mediated Golgi disruption all compromise axonal tubulin routing. We conclude that motor axons critically depend on axonal tubulin routing from the Golgi apparatus, a process that involves TBCE and possibly other tubulin chaperones.
轴突退变是运动神经元疾病最早出现的病理特征之一。我们在此研究了在微管蛋白特异性伴侣蛋白TBCE中发生突变的进行性运动神经元病(pmn)小鼠的潜在分子机制。我们证明,TBCE是一种与外周膜相关的蛋白,在高尔基体中积累。在pmn小鼠中,TBCE不稳定并从运动神经元的高尔基体中消失,并且微管在轴突远端丢失。轴突微管的丢失与轴突回退过程平行地逆行进行。这些退行性变化通过转基因TBCE互补以剂量依赖性方式受到抑制,该互补可恢复高尔基体处的TBCE表达。在培养的运动神经元中,pmn突变、RNA干扰介导的TBCE缺失以及布雷菲德菌素A介导的高尔基体破坏均损害轴突微管蛋白的运输。我们得出结论,运动轴突严重依赖于来自高尔基体的轴突微管蛋白运输,这一过程涉及TBCE以及可能的其他微管蛋白伴侣蛋白。