Matamoros Andrew J, Baas Peter W
Department of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA 19129, United States.
Department of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA 19129, United States.
Brain Res Bull. 2016 Sep;126(Pt 3):217-225. doi: 10.1016/j.brainresbull.2016.06.016. Epub 2016 Jun 27.
Microtubules are essential for the development and maintenance of axons and dendrites throughout the life of the neuron, and are vulnerable to degradation and disorganization in a variety of neurodegenerative diseases. Microtubules, polymers of tubulin heterodimers, are intrinsically polar structures with a plus end favored for assembly and disassembly and a minus end less favored for these dynamics. In the axon, microtubules are nearly uniformly oriented with plus ends out, whereas in dendrites, microtubules have mixed orientations. Microtubules in developing neurons typically have a stable domain toward the minus end and a labile domain toward the plus end. This domain structure becomes more complex during neuronal maturation when especially stable patches of polyaminated tubulin become more prominent within the microtubule. Microtubules are the substrates for molecular motor proteins that transport cargoes toward the plus or minus end of the microtubule, with motor-driven forces also responsible for organizing microtubules into their distinctive polarity patterns in axons and dendrites. A vast array of microtubule-regulatory proteins impart direct and indirect changes upon the microtubule arrays of the neuron, and these include microtubule-severing proteins as well as proteins responsible for the stability properties of the microtubules. During neurodegenerative diseases, microtubule mass is commonly diminished, and the potential exists for corruption of the microtubule polarity patterns and microtubule-mediated transport. These ill effects may be a primary causative factor in the disease or may be secondary effects, but regardless, therapeutics capable of correcting these microtubule abnormalities have great potential to improve the status of the degenerating nervous system.
微管对于神经元整个生命周期中轴突和树突的发育与维持至关重要,并且在多种神经退行性疾病中易发生降解和紊乱。微管是微管蛋白异二聚体的聚合物,是具有内在极性的结构,其正端有利于组装和拆卸,而负端则不太利于这些动态变化。在轴突中,微管几乎一致地以正端向外的方向排列,而在树突中,微管具有混合的方向。发育中的神经元中的微管通常在负端有一个稳定区域,在正端有一个不稳定区域。当尤其是多胺化微管蛋白的特别稳定的斑块在微管内变得更加突出时,这种区域结构在神经元成熟过程中会变得更加复杂。微管是分子运动蛋白的底物,这些蛋白将货物向微管的正端或负端运输,运动驱动的力也负责将微管组织成它们在轴突和树突中独特的极性模式。大量的微管调节蛋白对神经元的微管阵列产生直接和间接的变化,这些蛋白包括微管切断蛋白以及负责微管稳定性的蛋白。在神经退行性疾病期间,微管质量通常会减少,并且存在微管极性模式和微管介导的运输被破坏的可能性。这些不良影响可能是疾病的主要致病因素,也可能是次要影响,但无论如何,能够纠正这些微管异常的疗法具有极大的潜力来改善退化神经系统的状态。