Department of Respiratory and Sleep Medicine, Women's and Children's Hospital, Adelaide, Australia.
Gene Ther. 2012 Jan;19(1):8-14. doi: 10.1038/gt.2011.80. Epub 2011 Jun 9.
Although airway gene transfer research in mouse models relies on bolus fluid dosing into the nose or trachea, the dynamics and immediate fate of delivered gene transfer agents are poorly understood. In particular, this is because there are no in vivo methods able to accurately visualize the movement of fluid in small airways of intact animals. Using synchrotron phase-contrast X-ray imaging, we show that the fate of surrogate fluid doses delivered into live mouse airways can now be accurately and non-invasively monitored with high spatial and temporal resolution. This new imaging approach can help explain the non-homogenous distributions of gene expression observed in nasal airway gene transfer studies, suggests that substantial dose losses may occur at deliver into mouse trachea via immediate retrograde fluid motion and shows the influence of the speed of bolus delivery on the relative targeting of conducting and deeper lung airways. These findings provide insight into some of the factors that can influence gene expression in vivo, and this method provides a new approach to documenting and analyzing dose delivery in small-animal models.
虽然气道基因转移研究在小鼠模型中依赖于将流体团块注入鼻腔或气管,但传递的基因转移剂的动力学和即时命运仍知之甚少。特别是,这是因为目前还没有能够在完整动物的小气道中准确可视化流体运动的体内方法。我们使用同步加速器相衬 X 射线成像技术表明,现在可以以高时空分辨率准确和非侵入性地监测递送到活体小鼠气道中的替代流体剂量的命运。这种新的成像方法可以帮助解释在鼻气道基因转移研究中观察到的基因表达不均匀分布的现象,表明在通过即时逆行流体运动将大量剂量递送到小鼠气管时可能会发生大量剂量损失,并显示了流体团块传递速度对传导和更深肺部气道相对靶向的影响。这些发现为一些可以影响体内基因表达的因素提供了深入的了解,并且该方法为在小动物模型中记录和分析剂量传递提供了一种新方法。