腺相关病毒
少年
遗传增强
医学
遗产管理(遗嘱认证法)
病毒
病毒学
神经科学
基因
心理学
生物
载体(分子生物学)
政治学
遗传学
重组DNA
法学
作者
Alessandro Zappala,Heng Li,Ken Inoue
出处
期刊:Human Gene Therapy
[Mary Ann Liebert, Inc.]
日期:2024-11-25
卷期号:35 (23-24): 989-999
被引量:1
摘要
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.
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