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Development of a non-invasive optical imaging method for tracking vascular gene expression

机译:一种跟踪血管基因表达的非侵入光学成像方法的研制

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Gene therapy is an exciting frontier in modern medicine. To date, no imaging modalities are available for monitoring vascular gene therapy. Green fluorescent protein (GUP) has become an increasingly common marker for gene therapy. We have developed an optical imaging method to track vascular gene expression by detecting fluorescence emitted from GUP or red fluorescent protein (RUP) in arterial walls following gene transfer. We surgically transferred GFP- and RUP-vectors into the femoral and carotid arteries of three New Zealand white rabbits. Excitation light was transmitted through a fiber-optic ring-light (Nevoscope) and GUP and RUP fluorescence was detected by a charge coupled device (CCD) camera. Direct contact images of the target arteries demonstrated that this method was capable of both discriminating between normal and transferred arterial tissues and mapping fluorescent protein localization. Subsequent measurements by confocal microscopy showed statistically significant differences in average fluorescent signal intensity between the control and transferred tissues. This result was corroborated by immunohistochemical staining. These preliminary results are encouraging evidence that the optical imaging method can be developed further to be performed non-invasively and in vivo in a clinical setting.
机译:基因疗法是现代医学中的令人兴奋的前沿。迄今为止,没有用于监测血管基因治疗的成像方式。绿色荧光蛋白(GUP)已成为基因治疗的越来越常见的标志物。我们开发了一种光学成像方法,以通过检测在基因转移后动脉壁中的GUP或红色荧光蛋白(RUP)发射的荧光来跟踪血管基因表达。我们通过手术转移到三个新西兰白兔的股骨和颈动脉中的GFP和RUP-载体。激发光通过光纤环光(NEVISCOSCOSE)传递,并且通过电荷耦合装置(CCD)相机检测GUP和RUP荧光。目标动脉的直接接触图像证明了该方法能够在正常和转移的动脉组织之间区分和测绘荧光蛋白定位。共聚焦显微镜的后续测量显示了对照和转移组织之间的平均荧光信号强度的统计学显着差异。该结果通过免疫组织化学染色来证实。这些初步结果是令人令人抱怨的证据表明光学成像方法可以进一步开发,以便在临床环境中进行非侵入性和体内进行。

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