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A Near-Infrared Cell Tracker Reagent for Multiscopic In Vivo Imaging and Quantification of Leukocyte Immune Responses

机译:近红外细胞跟踪试剂用于多角度体内成像和白细胞免疫反应的量化。

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摘要

The complexity of the tumor microenvironment necessitates that cell behavior is studied in a broad, multi-scale context. Although tomographic and microscopy-based far and near infrared fluorescence (NIRF, >650 nm) imaging methods offer high resolution, sensitivity, and depth penetration, there has been a lack of optimized NIRF agents to label and track cells in their native environments at different scales. In this study we labeled mammalian leukocytes with VivoTag 680 (VT680), an amine reactive N-hydroxysuccinimide (NHS) ester of a (benz) indolium-derived far red fluorescent probe. We show that VT680 diffuses into leukocytes within minutes, covalently binds to cellular components, remains internalized for days in vitro and in vivo, and does not transfer fluorescence to adjacent cells. It is biocompatible, keeps cells fully functional, and fluoresces at high intensities. In a tumor model of cytotoxic T lymphocyte (CTL) immunotherapy, we track and quantify VT680-labeled cells longitudinally at the whole-body level with fluorescence-mediated molecular tomography (FMT), within tissues at single cell resolutions by multiphoton and confocal intravital microscopy, and ex vivo by flow cytometry. Thus, this approach is suitable to monitor cells at multiple resolutions in real time in their native environments by NIR-based fluorescence imaging.
机译:肿瘤微环境的复杂性使得必须在广泛,多尺度的背景下研究细胞行为。尽管基于层析和显微镜的远红外和近红外荧光(NIRF,> 650 nm)成像方法提供了高分辨率,灵敏度和深度穿透性,但仍缺乏优化的NIRF试剂来标记和跟踪其原始环境中不同细胞的情况秤。在这项研究中,我们用VivoTag 680(VT680)标记了哺乳动物白细胞,VivoTag 680是(苯)吲哚衍生的远红色荧光探针的胺反应性N-羟基琥珀酰亚胺(NHS)酯。我们显示,VT680在数分钟内扩散到白细胞中,与细胞成分共价结合,在体外和体内几天都被内在化,并且不会将荧光转移到相邻细胞中。它具有生物相容性,可以使细胞充分发挥功能,并在高强度下发出荧光。在细胞毒性T淋巴细胞(CTL)免疫治疗的肿瘤模型中,我们利用荧光介导的分子层析成像(FMT)在全身水平,通过多光子和共聚焦活体显微术以单个细胞分辨率在全身水平纵向跟踪和量化VT680标记的细胞。 ,并通过流式细胞仪进行离体。因此,该方法适用于通过基于NIR的荧光成像实时监控其原始环境中多个分辨率的细胞。

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