通过aav介导的CRISPR-Cas9组分的递送,在小鼠肺上皮中进行群体范围的基因破坏。

Molecular Therapy. Methods & Clinical Development Pub Date : 2022-11-01 eCollection Date: 2022-12-08 DOI:10.1016/j.omtm.2022.10.016
Honglin Chen, Steffen Durinck, Hetal Patel, Oded Foreman, Kathryn Mesh, Jeffrey Eastham, Roger Caothien, Robert J Newman, Merone Roose-Girma, Spyros Darmanis, Soren Warming, Annalisa Lattanzi, Yuxin Liang, Benjamin Haley
{"title":"通过aav介导的CRISPR-Cas9组分的递送,在小鼠肺上皮中进行群体范围的基因破坏。","authors":"Honglin Chen,&nbsp;Steffen Durinck,&nbsp;Hetal Patel,&nbsp;Oded Foreman,&nbsp;Kathryn Mesh,&nbsp;Jeffrey Eastham,&nbsp;Roger Caothien,&nbsp;Robert J Newman,&nbsp;Merone Roose-Girma,&nbsp;Spyros Darmanis,&nbsp;Soren Warming,&nbsp;Annalisa Lattanzi,&nbsp;Yuxin Liang,&nbsp;Benjamin Haley","doi":"10.1016/j.omtm.2022.10.016","DOIUrl":null,"url":null,"abstract":"<p><p>With the aim of expediting drug target discovery and validation for respiratory diseases, we developed an optimized method for <i>in situ</i> somatic gene disruption in murine lung epithelial cells via AAV6-mediated CRISPR-Cas9 delivery. Efficient gene editing was observed in lung type II alveolar epithelial cells and distal airway cells following assessment of single- or dual-guide AAV vector formats, Cas9 variants, and a sequential dosing strategy with combinatorial guide RNA expression cassettes. In particular, we were able to demonstrate population-wide gene disruption within distinct epithelial cell types for separate targets in Cas9 transgenic animals, with minimal to no associated inflammation. We also observed and characterized AAV vector integration events that occurred within directed double-stranded DNA break sites in lung cells, highlighting a complicating factor with AAV-mediated delivery of DNA nucleases. Taken together, we demonstrate a uniquely effective approach for somatic engineering of the murine lung, which will greatly facilitate the modeling of disease and therapeutic intervention.</p>","PeriodicalId":517056,"journal":{"name":"Molecular Therapy. Methods & Clinical Development","volume":" ","pages":"431-449"},"PeriodicalIF":0.0000,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/8f/29/main.PMC9668740.pdf","citationCount":"1","resultStr":"{\"title\":\"Population-wide gene disruption in the murine lung epithelium via AAV-mediated delivery of CRISPR-Cas9 components.\",\"authors\":\"Honglin Chen,&nbsp;Steffen Durinck,&nbsp;Hetal Patel,&nbsp;Oded Foreman,&nbsp;Kathryn Mesh,&nbsp;Jeffrey Eastham,&nbsp;Roger Caothien,&nbsp;Robert J Newman,&nbsp;Merone Roose-Girma,&nbsp;Spyros Darmanis,&nbsp;Soren Warming,&nbsp;Annalisa Lattanzi,&nbsp;Yuxin Liang,&nbsp;Benjamin Haley\",\"doi\":\"10.1016/j.omtm.2022.10.016\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>With the aim of expediting drug target discovery and validation for respiratory diseases, we developed an optimized method for <i>in situ</i> somatic gene disruption in murine lung epithelial cells via AAV6-mediated CRISPR-Cas9 delivery. Efficient gene editing was observed in lung type II alveolar epithelial cells and distal airway cells following assessment of single- or dual-guide AAV vector formats, Cas9 variants, and a sequential dosing strategy with combinatorial guide RNA expression cassettes. In particular, we were able to demonstrate population-wide gene disruption within distinct epithelial cell types for separate targets in Cas9 transgenic animals, with minimal to no associated inflammation. We also observed and characterized AAV vector integration events that occurred within directed double-stranded DNA break sites in lung cells, highlighting a complicating factor with AAV-mediated delivery of DNA nucleases. Taken together, we demonstrate a uniquely effective approach for somatic engineering of the murine lung, which will greatly facilitate the modeling of disease and therapeutic intervention.</p>\",\"PeriodicalId\":517056,\"journal\":{\"name\":\"Molecular Therapy. Methods & Clinical Development\",\"volume\":\" \",\"pages\":\"431-449\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/8f/29/main.PMC9668740.pdf\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Therapy. Methods & Clinical Development\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.omtm.2022.10.016\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/12/8 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Therapy. Methods & Clinical Development","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.omtm.2022.10.016","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/12/8 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

为了加速呼吸道疾病药物靶点的发现和验证,我们开发了一种优化的方法,通过aav6介导的CRISPR-Cas9递送,在小鼠肺上皮细胞中原位破坏体细胞基因。在评估单导或双导AAV载体格式、Cas9变体以及使用组合引导RNA表达盒的顺序给药策略后,在肺II型肺泡上皮细胞和远端气道细胞中观察到有效的基因编辑。特别是,我们能够在Cas9转基因动物中针对不同靶点的不同上皮细胞类型中证明群体范围内的基因破坏,并且很少甚至没有相关的炎症。我们还观察并表征了发生在肺细胞定向双链DNA断裂位点的AAV载体整合事件,强调了AAV介导的DNA核酸酶递送的复杂因素。综上所述,我们展示了一种独特有效的小鼠肺体细胞工程方法,这将极大地促进疾病建模和治疗干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Population-wide gene disruption in the murine lung epithelium via AAV-mediated delivery of CRISPR-Cas9 components.

Population-wide gene disruption in the murine lung epithelium via AAV-mediated delivery of CRISPR-Cas9 components.

Population-wide gene disruption in the murine lung epithelium via AAV-mediated delivery of CRISPR-Cas9 components.

Population-wide gene disruption in the murine lung epithelium via AAV-mediated delivery of CRISPR-Cas9 components.

With the aim of expediting drug target discovery and validation for respiratory diseases, we developed an optimized method for in situ somatic gene disruption in murine lung epithelial cells via AAV6-mediated CRISPR-Cas9 delivery. Efficient gene editing was observed in lung type II alveolar epithelial cells and distal airway cells following assessment of single- or dual-guide AAV vector formats, Cas9 variants, and a sequential dosing strategy with combinatorial guide RNA expression cassettes. In particular, we were able to demonstrate population-wide gene disruption within distinct epithelial cell types for separate targets in Cas9 transgenic animals, with minimal to no associated inflammation. We also observed and characterized AAV vector integration events that occurred within directed double-stranded DNA break sites in lung cells, highlighting a complicating factor with AAV-mediated delivery of DNA nucleases. Taken together, we demonstrate a uniquely effective approach for somatic engineering of the murine lung, which will greatly facilitate the modeling of disease and therapeutic intervention.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信