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轴突成束与解束的化学和机械控制

Chemical and mechanical control of axon fasciculation and defasciculation.

作者信息

Breau Marie Anne, Trembleau Alain

机构信息

Sorbonne Université, Centre National de la Recherche Scientifique (CNRS UMR 7622), Institut de Biologie Paris Seine (IBPS), Developmental Biology Laboratory, Paris, France.

Sorbonne Université, Centre National de la Recherche Scientifique (CNRS UMR8246), Inserm U1130, Institut de Biologie Paris Seine (IBPS), Neuroscience Paris Seine (NPS), Paris, France.

出版信息

Semin Cell Dev Biol. 2023 May 15;140:72-81. doi: 10.1016/j.semcdb.2022.06.014. Epub 2022 Jul 6.

Abstract

Neural networks are constructed through the development of robust axonal projections from individual neurons, which ultimately establish connections with their targets. In most animals, developing axons assemble in bundles to navigate collectively across various areas within the central nervous system or the periphery, before they separate from these bundles in order to find their specific targets. These processes, called fasciculation and defasciculation respectively, were thought for many years to be controlled chemically: while guidance cues may attract or repulse axonal growth cones, adhesion molecules expressed at the surface of axons mediate their fasciculation. Recently, an additional non-chemical parameter, the mechanical longitudinal tension of axons, turned out to play a role in axon fasciculation and defasciculation, through zippering and unzippering of axon shafts. In this review, we present an integrated view of the currently known chemical and mechanical control of axon:axon dynamic interactions. We highlight the facts that the decision to cross or not to cross another axon depends on a combination of chemical, mechanical and geometrical parameters, and that the decision to fasciculate/defasciculate through zippering/unzippering relies on the balance between axon:axon adhesion and their mechanical tension. Finally, we speculate about possible functional implications of zippering-dependent axon shaft fasciculation, in the collective migration of axons, and in the sorting of subpopulations of axons.

摘要

神经网络是通过单个神经元强大的轴突投射发展而构建的,这些轴突最终与它们的靶标建立连接。在大多数动物中,发育中的轴突聚集在一起形成束状,以便在中枢神经系统或外周的各个区域共同导航,然后它们从这些束中分离出来以找到它们的特定靶标。这两个过程分别称为成束和去束,多年来一直被认为是由化学物质控制的:引导线索可能吸引或排斥轴突生长锥,轴突表面表达的粘附分子介导它们的成束。最近,一个额外的非化学参数,即轴突的机械纵向张力,通过轴突轴的拉链式和非拉链式作用,在轴突成束和去束过程中发挥了作用。在这篇综述中,我们展示了目前已知的轴突与轴突动态相互作用的化学和机械控制的综合观点。我们强调这样的事实,即决定是否穿过另一条轴突取决于化学、机械和几何参数的组合,并且通过拉链式/非拉链式进行成束/去束的决定依赖于轴突与轴突之间的粘附力和它们的机械张力之间的平衡。最后,我们推测了依赖拉链式的轴突轴成束在轴突的集体迁移以及轴突亚群的分类中的可能功能意义。

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