Synaptic Function Section, The Porter Neuroscience Research Center, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
J Cell Biol. 2024 Jun 3;223(6). doi: 10.1083/jcb.202401145. Epub 2024 Apr 3.
Disruption of synapse assembly and maturation leads to a broad spectrum of neurodevelopmental disorders. Presynaptic proteins are largely synthesized in the soma, where they are packaged into precursor vesicles and transported into distal axons to ensure precise assembly and maintenance of presynapses. Due to their morphological features, neurons face challenges in the delivery of presynaptic cargos to nascent boutons. Thus, targeted axonal transport is vital to build functional synapses. A growing number of mutations in genes encoding the transport machinery have been linked to neurodevelopmental disorders. Emerging lines of evidence have started to uncover presynaptic mechanisms underlying axonal transport defects, thus broadening the view of neurodevelopmental disorders beyond postsynaptic mechanisms. In this review, we discuss presynaptic perspectives of neurodevelopmental disorders by focusing on impaired axonal transport and disturbed assembly and maintenance of presynapses. We also discuss potential strategies for restoring axonal transport as an early therapeutic intervention.
突触组装和成熟的破坏会导致广泛的神经发育障碍。突触前蛋白主要在胞体中合成,在那里它们被包装到前体小泡中,并运输到远端轴突,以确保精确组装和维持突触前。由于神经元的形态特征,它们在将突触前 cargos 递送到新生末梢时面临挑战。因此,靶向轴突运输对于建立功能性突触至关重要。越来越多的编码运输机制的基因突变与神经发育障碍有关。新出现的证据表明,已经开始揭示轴突运输缺陷的突触前机制,从而将神经发育障碍的观点从突触后机制扩展到更广泛的范围。在这篇综述中,我们通过关注受损的轴突运输以及突触前的组装和维持障碍,讨论了神经发育障碍的突触前观点。我们还讨论了作为早期治疗干预的恢复轴突运输的潜在策略。