Department of Neuroscience, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.
Discovery Theme on Chronic Brain Injury, The Ohio State University, Columbus, OH, USA.
Dev Neurobiol. 2020 Jul;80(7-8):277-301. doi: 10.1002/dneu.22780. Epub 2020 Sep 28.
Axons in the adult mammalian central nervous system (CNS) fail to regenerate inside out due to intrinsic and extrinsic neuronal determinants. During CNS development, axon growth, synapse formation, and function are tightly regulated processes allowing immature neurons to effectively grow an axon, navigate toward target areas, form synaptic contacts and become part of information processing networks that control behavior in adulthood. Not only immature neurons are able to precisely control the expression of a plethora of genes necessary for axon extension and pathfinding, synapse formation and function, but also non-neuronal cells such as astrocytes and microglia actively participate in sculpting the nervous system through refinement, consolidation, and elimination of synaptic contacts. Recent evidence indicates that a balancing act between axon regeneration and synaptic function may be crucial for rebuilding functional neuronal circuits after CNS trauma and disease in adulthood. Here, we review the role of classical and new intrinsic and extrinsic neuronal determinants in the context of CNS development, injury, and disease. Moreover, we discuss strategies targeting neuronal and non-neuronal cell behaviors, either alone or in combination, to promote axon regeneration and neuronal circuit formation in adulthood.
轴突在成年哺乳动物中枢神经系统 (CNS) 中无法再生,这是由于内在和外在神经元决定因素所致。在 CNS 发育过程中,轴突生长、突触形成和功能是受到严格调控的过程,使未成熟神经元能够有效地生长轴突、向靶区导航、形成突触接触,并成为控制成年行为的信息处理网络的一部分。不仅未成熟神经元能够精确控制多种基因的表达,这些基因对于轴突延伸和导向、突触形成和功能是必需的,而且星形胶质细胞和小胶质细胞等非神经元细胞也通过对突触接触的细化、巩固和消除,积极参与神经系统的塑造。最近的证据表明,在成年期 CNS 创伤和疾病后重建功能性神经元回路,轴突再生和突触功能之间的平衡可能是至关重要的。在这里,我们综述了经典和新的内在和外在神经元决定因素在 CNS 发育、损伤和疾病中的作用。此外,我们讨论了单独或联合靶向神经元和非神经元细胞行为的策略,以促进成年期轴突再生和神经元回路形成。