Lobe-Specific Gene Vector Delivery to Rat Lungs Using a Miniature Bronchoscope.

Q1 Immunology and Microbiology Human Gene Therapy Methods Pub Date : 2018-10-01 Epub Date: 2018-08-10 DOI:10.1089/hgtb.2018.050
Chantelle McIntyre, Martin Donnelley, Nathan Rout-Pitt, David Parsons
{"title":"Lobe-Specific Gene Vector Delivery to Rat Lungs Using a Miniature Bronchoscope.","authors":"Chantelle McIntyre,&nbsp;Martin Donnelley,&nbsp;Nathan Rout-Pitt,&nbsp;David Parsons","doi":"10.1089/hgtb.2018.050","DOIUrl":null,"url":null,"abstract":"<p><p>For respiratory research utilizing gene vector delivery to the lung, the size of rodent models has typically necessitated relatively \"blind\" dosing via the nose, via an endotracheal tube, or through a surgical incision into the trachea. This commonly results in a limited ability to dose specific small regions of the lung reliably, and contributes to high levels of transduction variability between animals. The resultant poor reliability, reproducibility, and high variability compromises statistical capability, and so demands greater animal sample sizes than should be feasible. The first reliable targeted gene vector dosing of small regions in rat lungs has been designed and successfully implemented using a miniature rigid bronchoscope containing a working channel. Using this setup, this technique can currently access airway branches down to at least the fourth generation in the lungs of rats >200 g in body weight, allowing dosing and re-dosing of specific lobes via airway branch points in the lung tree. Here, the protocol for performing this minimally invasive technique is reported, along with the effect of delivering vesicular stomatitis virus G pseudotyped lentivirus to selected lung lobes. Examples of other applications, such as delivery of agar beads, are also shown. It is expected that the availability of this technique will substantially enhance gene vector studies in rat models for a range of lung diseases.</p>","PeriodicalId":13126,"journal":{"name":"Human Gene Therapy Methods","volume":"29 5","pages":"228-235"},"PeriodicalIF":0.0000,"publicationDate":"2018-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/hgtb.2018.050","citationCount":"14","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Gene Therapy Methods","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1089/hgtb.2018.050","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2018/8/10 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 14

Abstract

For respiratory research utilizing gene vector delivery to the lung, the size of rodent models has typically necessitated relatively "blind" dosing via the nose, via an endotracheal tube, or through a surgical incision into the trachea. This commonly results in a limited ability to dose specific small regions of the lung reliably, and contributes to high levels of transduction variability between animals. The resultant poor reliability, reproducibility, and high variability compromises statistical capability, and so demands greater animal sample sizes than should be feasible. The first reliable targeted gene vector dosing of small regions in rat lungs has been designed and successfully implemented using a miniature rigid bronchoscope containing a working channel. Using this setup, this technique can currently access airway branches down to at least the fourth generation in the lungs of rats >200 g in body weight, allowing dosing and re-dosing of specific lobes via airway branch points in the lung tree. Here, the protocol for performing this minimally invasive technique is reported, along with the effect of delivering vesicular stomatitis virus G pseudotyped lentivirus to selected lung lobes. Examples of other applications, such as delivery of agar beads, are also shown. It is expected that the availability of this technique will substantially enhance gene vector studies in rat models for a range of lung diseases.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
利用微型支气管镜向大鼠肺输送肺叶特异性基因载体。
对于利用基因载体传递到肺部的呼吸研究,啮齿动物模型的大小通常需要通过鼻子,通过气管内管或通过手术切口进入气管进行相对“盲目”的给药。这通常导致对肺特定小区域进行可靠剂量的能力有限,并导致动物之间高水平的转导变异性。由此产生的低可靠性、可重复性和高可变性损害了统计能力,因此需要比可行的更大的动物样本量。使用包含工作通道的微型刚性支气管镜,设计并成功实现了大鼠肺小区域可靠的靶向基因载体剂量。使用这种设置,该技术目前可以进入体重> 200g的大鼠肺中至少第四代的气道分支,允许通过肺树中的气道分支点给药和再给药特定的肺叶。本文报道了实施这种微创技术的方案,以及将水疱性口炎病毒G伪型慢病毒输送到选定的肺叶的效果。其他应用的例子,如琼脂珠的交付,也显示。预计这项技术的可用性将大大加强基因载体在大鼠模型中研究一系列肺部疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Human Gene Therapy Methods
Human Gene Therapy Methods BIOTECHNOLOGY & APPLIED MICROBIOLOGY-GENETICS & HEREDITY
CiteScore
5.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Human Gene Therapy is the premier, multidisciplinary journal covering all aspects of gene therapy. The Journal publishes in-depth coverage of DNA, RNA, and cell therapies by delivering the latest breakthroughs in research and technologies. Human Gene Therapy provides a central forum for scientific and clinical information, including ethical, legal, regulatory, social, and commercial issues, which enables the advancement and progress of therapeutic procedures leading to improved patient outcomes, and ultimately, to curing diseases. The Journal is divided into three parts. Human Gene Therapy, the flagship, is published 12 times per year. HGT Methods, a bimonthly journal, focuses on the applications of gene therapy to product testing and development. HGT Clinical Development, a quarterly journal, serves as a venue for publishing data relevant to the regulatory review and commercial development of cell and gene therapy products.
期刊最新文献
Lot-to-Lot Variation in Adeno-Associated Virus Serotype 9 (AAV9) Preparations. Fast-Seq: A Simple Method for Rapid and Inexpensive Validation of Packaged Single-Stranded Adeno-Associated Viral Genomes in Academic Settings. LINC00958 Accelerates Cell Proliferation and Migration in Non-Small Cell Lung Cancer Through JNK/c-JUN Signaling. Nanoparticle Tracking of Adenovirus by Light Scattering and Fluorescence Detection. LINC00958 accelerates cell proliferation and migration in non-small cell lung cancer through JNK/c-JUN signaling.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1