量子点对淋巴结中动态白细胞迁移的多光谱双光子成像的综合评价

IntraVital Pub Date : 2013-04-01 DOI:10.4161/intv.25745
D. Natale, S. Soriano, F. Coelho, Miroslav Hons, J. Stein
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引用次数: 2

摘要

近年来,活体双光子显微镜(2PM)已成为活体麻醉小鼠外周淋巴结(pln)内免疫细胞动力学直接原位成像的合适技术,对免疫反应的调节提供了重要的见解。然而,大多数目前的2PM方法受到近红外(NIR)探针用于多光谱延时成像的稀缺性以及使用单一激发波长用于多个荧光团的限制。最近可用的量子点(QDs)纳米颗粒具有独特的光学特性,有可能克服这一限制,但其适用性尚未全面测试用于体内2PM成像。在这项研究中,我们探索了nir发射量子点在树突状细胞中的使用和传递。此外,我们用抗体功能化这些纳米颗粒的表面,这些抗体可以识别在PLN微血管内皮上表达的特定抗原或将其用作近红外血浆标记物,并检测淋巴细胞的稳态再循环。这种方法允许同时可视化多达六种不同的细胞群和淋巴样结构,并确定在确定的微环境中不同的淋巴细胞迁移模式。然而,量子点更难与抗体重复偶联,并有引起目标抗原聚集的倾向。我们的数据深入分析了量子点作为2PM研究中解剖地标成像工具的有用性和缺点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive assessment of quantum dots for multispectral twophoton imaging of dynamic leukocyte migration in lymph nodes
In recent years, intravital twophoton microscopy (2PM) has emerged as the appropriate technique for direct in situ imaging of immune cell dynamics inside peripheral lymph nodes (PLNs) of live, anesthetized mice, yielding important insights into the regulation of immune responses. However, most current 2PM approaches are limited by the scarce availability of near-infrared (NIR) probes for multispectral time-lapse imaging, and by the use of a single excitation wavelength for multiple fluorophores. The recent availability of quantum dots (QDs) nanoparticles displaying unique optical properties have the potential to overcome this limitation but their suitability has not been yet comprehensively tested for 2PM imaging in vivo. In this study, we explored the use and delivery of NIR-emitting QDs into dendritic cells. Furthermore, we functionalized the surface of these nanoparticles with antibodies that recognize specific antigens expressed on the endothelium of the PLN microvasculature or their use as NIR plasma markers and examined the homeostatic recirculation of lymphocytes. This approach allowed to simultaneously visualize up to six different cell populations and lymphoid structures and identified varying lymphocyte migration patterns in defined microenvironments. Yet, QDs were more difficult to reproducibly couple to antibodies and showed a tendency to cause clustering of targeted antigens. Our data provide an in-depth analysis of the usefulness and shortcomings of QDs as imaging tools for anatomical landmarking in 2PM studies.
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