Zappala Alessandro, Li Heng, Inoue Ken
Department Mental Retardation & Birth Defect Research, National Center of Neurology & Psychiatry, National Institute of Neuroscience, Tokyo, Japan.
Hum Gene Ther. 2024 Dec;35(23-24):989-999. doi: 10.1089/hum.2024.108. Epub 2024 Nov 25.
Systemic delivery of adeno-associated virus (AAV) vectors targeting the central nervous system has the potential to solve many neurodevelopmental disorders, yet it is made difficult by the filtering effect of the blood-brain barrier and systemic complications. To overcome this limitation, we attempted to inject a Venus-expressing, oligodendrocyte-selective AAV9 viral vector in the ventricles together with lipid microbubbles and subjected them to focused ultrasound (FUS); the resulting mechanical stimulation on the brain ventricles is able to open small, temporary gaps from which vector particles can leak and spread. Our findings indicate that FUS can increase viral vector diffusion across both the anteroposterior and left-right axes without influencing cell tropism; significant effects were found with 60 and 90 s exposure time, but no effects were observed with longer intervals. Taken together, these results highlight a new strategy for the safe and effective delivery of viral vectors and offer new perspectives for the development and application of gene therapies for central nervous system diseases.
系统性递送靶向中枢神经系统的腺相关病毒(AAV)载体有潜力解决许多神经发育障碍问题,但血脑屏障的过滤作用和全身并发症使其面临困难。为克服这一限制,我们尝试将表达金星蛋白的少突胶质细胞选择性AAV9病毒载体与脂质微泡一起注入脑室,并对其施加聚焦超声(FUS);由此产生的对脑室的机械刺激能够打开小的临时间隙,载体颗粒可从中泄漏和扩散。我们的研究结果表明,FUS可增加病毒载体在前后轴和左右轴上的扩散,而不影响细胞嗜性;在60秒和90秒的暴露时间下发现了显著效果,但更长时间间隔未观察到效果。综上所述,这些结果突出了一种安全有效递送病毒载体的新策略,并为中枢神经系统疾病基因治疗的开发和应用提供了新的视角。