A Comprehensive Atlas of AAV Tropism in the Mouse

Christopher J. Walkey, Kathy J. Snow, Jote Bulcha, Aaron R. Cox, Alexa E. Martinez, M. Cecilia Ljungberg, Denise G. Lanza, Marco De Giorgi, Marcel A. Chuecos, Michele Alves-Bezerra, Carlos Flores Suarez, Sean M. Hartig, Susan G. Hilsenbeck, Chih-Wei Hsu, Ethan Saville, Yaned Gaitan, Jeff Duryea, Seth Hannigan, Mary E. Dickinson, Oleg Mirochnitchenko, Dan Wang, Cathleen M. Lutz, Jason D. Heaney, Guangping Gao, Steve A. Murray, William R. Lagor
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Abstract

Gene therapy with Adeno-Associated Viral (AAV) vectors requires knowledge of their tropism within the body. Here we analyze the tropism of ten naturally occurring AAV serotypes (AAV3B, AAV4, AAV5, AAV6, AAV7, AAV8, AAV9, AAVrh8, AAVrh10 and AAVrh74) following systemic delivery into male and female mice. A transgene expressing ZsGreen and Cre recombinase was used to identify transduction in a cell-dependent manner based on fluorescence. Cre-driven activation of tdTomato fluorescence offered superior sensitivity for transduced cells. All serotypes except AAV3B and AAV4 had high liver tropism. Fluorescence activation revealed transduction of unexpected tissues, including adrenals, testes and ovaries. Rare transduced cells within tissues were also readily visualized. Biodistribution of AAV genomes correlated with fluorescence, except in immune tissues. AAV4 was found to have a pan-endothelial tropism while also targeting pancreatic beta cells. This public resource enables selection of the best AAV serotypes for basic science and preclinical applications in mice.
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小鼠 AAV Tropism 综合图谱
使用腺相关病毒(AAV)载体进行基因治疗需要了解它们在体内的趋向性。在这里,我们分析了十种天然存在的 AAV 血清型(AAV3B、AAV4、AAV5、AAV6、AAV7、AAV8、AAV9、AAVrh8、AAVrh10 和 AAVrh74)在雌性和雄性小鼠体内输送后的趋向性。利用表达 ZsGreen 和 Cre 重组酶的转基因,以荧光为基础确定依赖细胞的转导方式。Cre驱动的tdTomato荧光激活为转导细胞提供了更高的灵敏度。除 AAV3B 和 AAV4 外,所有血清型都具有较高的肝脏滋养性。荧光激活显示转导了意想不到的组织,包括肾上腺、睾丸和卵巢。组织内罕见的转导细胞也很容易被观察到。除免疫组织外,AAV 基因组的生物分布与荧光相关。研究发现,AAV4具有泛内皮滋养特性,同时也能靶向胰腺β细胞。这一公共资源有助于为基础科学和小鼠临床前应用选择最佳的 AAV 血清型。
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