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声靶向非侵入性基因治疗在大的脑体积。

Acoustically targeted noninvasive gene therapy in large brain volumes.

机构信息

Department of Bioengineering, Rice University, Houston, TX, 77030, USA.

Rice Neuroengineering Initiative, Rice University, Houston, TX, 77030, USA.

出版信息

Gene Ther. 2024 Mar;31(3-4):85-94. doi: 10.1038/s41434-023-00421-1. Epub 2023 Sep 12.

DOI:10.1038/s41434-023-00421-1
PMID:37696982
Abstract

Focused Ultrasound Blood-Brain Barrier Opening (FUS-BBBO) can deliver adeno-associated viral vectors (AAVs) to treat genetic disorders of the brain. However, such disorders often affect large brain regions. Moreover, the applicability of FUS-BBBO in the treatment of brain-wide genetic disorders has not yet been evaluated. Herein, we evaluated the transduction efficiency and safety of opening up to 105 sites simultaneously. Increasing the number of targeted sites increased gene delivery efficiency at each site. We achieved transduction of up to 60% of brain cells with comparable efficiency in the majority of the brain regions. Furthermore, gene delivery with FUS-BBBO was safe even when all 105 sites were targeted simultaneously without negative effects on animal weight or neuronal loss. To evaluate the application of multi-site FUS-BBBO for gene therapy, we used it for gene editing using the clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated 9 (Cas9) system and found effective gene editing, but also a loss of neurons at the targeted sites. Overall, this study provides a brain-wide map of transduction efficiency, shows the synergistic effect of multi-site targeting on transduction efficiency, and is the first example of large brain volume gene editing after noninvasive gene delivery with FUS-BBBO.

摘要

聚焦超声血脑屏障开放(FUS-BBBO)可将腺相关病毒载体(AAV)递送至大脑,以治疗遗传性脑部疾病。然而,此类疾病通常会影响大脑的大片区域。此外,FUS-BBBO 在治疗全脑遗传性疾病中的适用性尚未得到评估。在此,我们评估了同时打开多达 105 个靶点的转导效率和安全性。增加靶向靶点的数量会提高每个靶点的基因传递效率。我们实现了高达 60%的脑细胞转导,且在大多数脑区的效率相当。此外,即使同时靶向所有 105 个靶点,FUS-BBBO 的基因传递也是安全的,不会对动物体重或神经元丢失产生负面影响。为了评估多靶点 FUS-BBBO 在基因治疗中的应用,我们使用其进行基于簇状规则间隔短回文重复序列(CRISPR)/CRISPR 相关蛋白 9(Cas9)系统的基因编辑,发现了有效的基因编辑,但也存在靶向部位神经元丢失的情况。总的来说,这项研究提供了大脑转导效率的全脑图谱,显示了多靶点靶向对转导效率的协同作用,并且是 FUS-BBBO 进行非侵入性基因传递后进行大体积大脑基因编辑的首例。

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本文引用的文献

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Focused ultrasound-mediated brain genome editing.聚焦超声介导的大脑基因编辑。
Proc Natl Acad Sci U S A. 2023 Aug 22;120(34):e2302910120. doi: 10.1073/pnas.2302910120. Epub 2023 Aug 14.
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Efficacy of gene delivery to the brain using AAV and ultrasound depends on serotypes and brain areas.使用 AAV 和超声将基因递送到大脑的效果取决于血清型和大脑区域。
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Engineering viral vectors for acoustically targeted gene delivery.工程化病毒载体用于声靶向基因传递。
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超声介导基因传递和红光激发的非侵入性光遗传学。
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