体内
星形胶质细胞
祖细胞
转基因
病毒载体
向性
细胞生物学
淋巴系统
全身给药
生物
少突胶质细胞
神经干细胞
病毒学
载体(分子生物学)
多发性硬化
基因传递
神经胶质
人脑
免疫学
遗传增强
化学
转染
离体
干细胞
神经球
胶质增生
医学
病毒
细胞
转基因小鼠
作者
Alexander Cona,Evan Newbold,Deniz Kesmen,Rajiv Snape,Jessica Danner,Nicholas White,William Borden,Abigail Iseson,Steven J. Schanz,Devin Chandler-Militello,X Li,Jose C. Cano,John N. Mariani,Maiken Nedergaard,Abdellatif Benraiss,Steven A. Goldman
标识
DOI:10.1038/s41587-026-03185-2
摘要
Treatment of neurological diseases that involve oligodendrocytes or astrocytes would benefit from the selective delivery of viral vectors to their common parent, glial progenitor cells (GPCs). Here, we select adeno-associated virus (AAV) capsids with tropism for human GPCs and demonstrate efficient and widespread delivery of the resultant AAVs throughout the mouse brain through the glymphatic system. In vivo screening of a library of capsid-modified, recombination-reported AAVs in chimeric mice engrafted with PDGFRA-driven Cre recombinase-expressing human GPCs identified a set of AAV5-based vectors that preferentially infect human GPCs and/or their astrocyte and oligodendrocyte progeny in vivo, with minimal systemic infection. To maximize the intracerebral distribution of these vectors while minimizing their dosing and extracerebral spread, we paired intracisternal delivery with systemic hypertonicity to increase glymphatic influx. This method bypasses the blood-brain barrier, delivering AAV directly into the brain parenchyma. Glymphatic delivery of our capsid-modified AAV5s enables efficient transgene delivery to human glia throughout the entire adult mouse brain, with minimal off-target transduction.
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