Saito Atsushi, Cavalli Valeria
From the ‡Department of Anatomy and Neurobiology, Washington University in St Louis, School of Medicine, St Louis, 63110, Missouri.
Mol Cell Proteomics. 2016 Feb;15(2):382-93. doi: 10.1074/mcp.R115.052753. Epub 2015 Aug 21.
Neurons are extremely polarized cells. Axon lengths often exceed the dimension of the neuronal cell body by several orders of magnitude. These extreme axonal lengths imply that neurons have mastered efficient mechanisms for long distance signaling between soma and synaptic terminal. These elaborate mechanisms are required for neuronal development and maintenance of the nervous system. Neurons can fine-tune long distance signaling through calcium wave propagation and bidirectional transport of proteins, vesicles, and mRNAs along microtubules. The signal transmission over extreme lengths also ensures that information about axon injury is communicated to the soma and allows for repair mechanisms to be engaged. This review focuses on the different mechanisms employed by neurons to signal over long axonal distances and how signals are interpreted in the soma, with an emphasis on proteomic studies. We also discuss how proteomic approaches could help further deciphering the signaling mechanisms operating over long distance in axons.
神经元是极具极性的细胞。轴突长度通常比神经元细胞体的尺寸超出几个数量级。这些极长的轴突长度意味着神经元已经掌握了在胞体和突触末端之间进行高效长距离信号传递的机制。这些精细的机制对于神经元发育和神经系统的维持是必需的。神经元可以通过钙波传播以及蛋白质、囊泡和信使核糖核酸沿微管的双向运输来微调长距离信号传递。在极长距离上的信号传递还确保了有关轴突损伤的信息能够传递到胞体,并使得修复机制得以启动。本综述重点关注神经元用于在长轴突距离上进行信号传递的不同机制,以及这些信号在胞体中是如何被解读的,尤其着重于蛋白质组学研究。我们还将讨论蛋白质组学方法如何有助于进一步破译在轴突中长距离运作的信号传导机制。