Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL.
Beckman Institute for Advanced Science and Technology, Urbana, IL.
Theranostics. 2020 Jan 1;10(4):1733-1745. doi: 10.7150/thno.36022. eCollection 2020.
: Peripheral arterial disease (PAD) is a major worldwide health concern. Since the late 1990s therapeutic angiogenesis has been investigated as an alternative to traditional PAD treatments. Although positive preclinical results abound in the literature, the outcomes of human clinical trials have been discouraging. Among the challenges the field has faced has been a lack of standardization of the timings and measures used to validate new treatment approaches. : In order to study the spatiotemporal dynamics of both perfusion and neovascularization in mice subjected to surgically-induced hindlimb ischemia (n= 30), we employed three label-free imaging modalities (a novel high-sensitivity ultrasonic Power Doppler methodology, laser speckle contrast, and photoacoustic imaging), as well as a tandem of radio-labeled molecular probes, Tc-NC100692 and Tc-BRU-5921 respectively, designed to detect two key modulators of angiogenic activity, and HIF-1α , via scintigraphic imaging. : The multimodal imaging strategy reveals a set of "landmarks"-key physiological and molecular events in the healing process-that can serve as a standardized framework for describing the impact of emerging PAD treatments. These landmarks span the entire process of neovascularization, beginning with the rapid decreases in perfusion and oxygenation associated with ligation surgery, extending through pro-angiogenic changes in gene expression driven by the master regulator HIF-1α , and ultimately leading to complete functional revascularization of the affected tissues. : This study represents an important step in the development of multimodal non-invasive imaging strategies for vascular research; the combined results offer more insight than can be gleaned through any of the individual imaging methods alone. Researchers adopting similar imaging strategies and will be better able to describe changes in the onset, duration, and strength of each of the landmarks of vascular recovery, yielding greater biological insight, and enabling more comprehensive cross-study comparisons. Perhaps most important, this study paves the road for more efficient translation of PAD research; emerging experimental treatments can be more effectively assessed and refined at the preclinical stage, ultimately leading to better next-generation therapies.
外周动脉疾病(PAD)是一个全球性的主要健康问题。自 20 世纪 90 年代末以来,治疗性血管生成已被作为传统 PAD 治疗的替代方法进行研究。尽管文献中充满了积极的临床前结果,但人体临床试验的结果却令人沮丧。该领域面临的挑战之一是缺乏用于验证新治疗方法的时间和措施的标准化。
为了研究手术诱导的后肢缺血(n=30)小鼠中灌注和新生血管形成的时空动态,我们采用了三种无标记成像方式(一种新颖的高灵敏度超声功率多普勒方法、激光散斑对比和光声成像),以及一对放射性标记的分子探针,Tc-NC100692 和 Tc-BRU-5921,分别设计用于通过闪烁成像检测两种关键的血管生成活性调节剂, 和 HIF-1α。
多模态成像策略揭示了一组“地标”-愈合过程中的关键生理和分子事件-可作为描述新兴 PAD 治疗影响的标准化框架。这些地标涵盖了新生血管形成的整个过程,从结扎手术相关的灌注和氧合快速下降开始,扩展到由主调控因子 HIF-1α驱动的基因表达的促血管生成变化,最终导致受影响组织的完全功能再血管化。
这项研究代表了血管研究中多模态非侵入性成像策略发展的重要一步;综合结果提供了比任何单一成像方法单独获得的更多的见解。采用类似成像策略的研究人员将能够更好地描述血管恢复的每个地标起始、持续时间和强度的变化,从而获得更大的生物学洞察力,并实现更全面的跨研究比较。也许最重要的是,这项研究为 PAD 研究的更有效转化铺平了道路;新兴的实验性治疗方法可以在临床前阶段更有效地进行评估和改进,最终导致更好的下一代治疗方法。