Department of Molecular Pharmacology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo 187-8502, Japan.
Department of NCNP Brain Physiology and Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.
J Neurosci. 2024 Oct 23;44(43):e1593232024. doi: 10.1523/JNEUROSCI.1593-23.2024.
Injuries to the central nervous system (CNS) can cause severe neurological deficits. Axonal regrowth is a fundamental process for the reconstruction of compensatory neuronal networks after injury; however, it is extremely limited in the adult mammalian CNS. In this study, we conducted a loss-of-function genetic screen in cortical neurons, combined with a Web resource-based phenotypic screen, and identified synaptotagmin 4 (Syt4) as a novel regulator of axon elongation. Silencing Syt4 in primary cultured cortical neurons inhibits neurite elongation, with changes in gene expression involved in signaling pathways related to neuronal development. In a spinal cord injury model, inhibition of Syt4 expression in cortical neurons prevented axonal sprouting of the corticospinal tract, as well as neurological recovery after injury. These results provide a novel therapeutic approach to CNS injury by modulating Syt4 function.
中枢神经系统 (CNS) 的损伤可导致严重的神经功能缺损。轴突再生是损伤后重建代偿性神经元网络的基本过程;然而,在成年哺乳动物的中枢神经系统中,其再生能力极其有限。在这项研究中,我们在皮质神经元中进行了功能丧失的遗传筛选,结合基于网络资源的表型筛选,鉴定出突触结合蛋白 4 (Syt4) 是轴突伸长的一个新的调节因子。在原代培养的皮质神经元中沉默 Syt4 可抑制神经突的伸长,基因表达的变化涉及与神经元发育相关的信号通路。在脊髓损伤模型中,抑制皮质神经元中 Syt4 的表达可防止皮质脊髓束的轴突发芽,以及损伤后的神经功能恢复。这些结果通过调节 Syt4 功能为中枢神经系统损伤提供了一种新的治疗方法。