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使用微型支气管镜将叶特异性基因载体递送至大鼠肺部。

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

作者信息

McIntyre Chantelle, Donnelley Martin, Rout-Pitt Nathan, Parsons David

机构信息

1 Robinson Research Institute, University of Adelaide , Adelaide, South Australia .

2 Adelaide Medical School, University of Adelaide , Adelaide, South Australia .

出版信息

Hum Gene Ther Methods. 2018 Oct;29(5):228-235. doi: 10.1089/hgtb.2018.050. Epub 2018 Aug 10.

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.

摘要

对于利用基因载体递送至肺部进行的呼吸研究,啮齿动物模型的大小通常需要通过鼻腔、气管插管或通过气管手术切口进行相对“盲目”给药。这通常导致可靠地对肺的特定小区域给药的能力有限,并导致动物之间转导变异性水平较高。由此产生的可靠性差、可重复性差和高变异性损害了统计能力,因此需要比可行情况下更大的动物样本量。使用包含工作通道的微型硬质支气管镜,设计并成功实施了首次对大鼠肺部小区域进行可靠的靶向基因载体给药。使用这种设置,该技术目前可以进入体重>200 g大鼠肺部至少第四代的气道分支,从而通过肺树中的气道分支点对特定肺叶进行给药和重新给药。在此,报告了执行这种微创技术的方案,以及将水泡性口炎病毒G假型慢病毒递送至选定肺叶的效果。还展示了其他应用的示例,如琼脂珠的递送。预计该技术的可用性将大大加强大鼠模型中针对一系列肺部疾病的基因载体研究。

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