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A Versatile Technique for the In Vivo Imaging of Human Tumor Xenografts Using Near-Infrared Fluorochrome-Conjugated Macromolecule Probes

机译:使用近红外荧光染料缀合的大分子探针对人类肿瘤异种移植进行体内成像的多功能技术。

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摘要

Here, we present a versatile method for detecting human tumor xenografts in vivo, based on the enhanced permeability and retention (EPR) effect, using near-infrared (NIR) fluorochrome-conjugated macromolecule probes. Bovine serum albumin (BSA) and two immunoglobulins—an anti-human leukocyte antigen (HLA) monoclonal antibody and isotype control IgG2a—were labeled with XenoLight CF770 fluorochrome and used as NIR-conjugated macromolecule probes to study whole-body imaging in a variety of xenotransplantation mouse models. NIR fluorescent signals were observed in subcutaneously transplanted BxPC-3 (human pancreatic cancer) cells and HCT 116 (colorectal cancer) cells within 24 h of NIR-macromolecule probe injection, but the signal from the fluorochrome itself or from the NIR-conjugated small molecule (glycine) injection was not observed. The accuracy of tumor targeting was confirmed by the localization of the NIR-conjugated immunoglobulin within the T-HCT 116 xenograft (in which the orange-red fluorescent protein tdTomato was stably expressed by HCT 116 cells) in the subcutaneous transplantation model. However, there was no significant difference in the NIR signal intensity of the region of interest between the anti-HLA antibody group and the isotype control group in the subcutaneous transplantation model. Therefore, the antibody accumulation within the tumor in vivo is based on the EPR effect. The liver metastasis generated by an intrasplenic injection of T-HCT 116 cells was clearly visualized by the NIR-conjugated anti-HLA probe but not by the orange-red fluorescent signal derived from the tdTomato reporter. This result demonstrated the superiority of the NIR probes over the tdTomato reporter protein at enhancing tissue penetration. In another xenograft model, patient-derived xenografts (PDX) of LC11-JCK (human non-small cell lung cancer) were successfully visualized using the NIR-conjugated macromolecule probe without any genetic modification. These results suggested that NIR-conjugated macromolecule, preferably, anti-HLA antibody probe is a valuable tool for the detection of human tumors in experimental metastasis models using whole-body imaging.
机译:在这里,我们提出一种利用近红外(NIR)荧光染料偶联的大分子探针,基于增强的通透性和保留(EPR)效果,在体内检测人肿瘤异种移植物的通用方法。牛血清白蛋白(BSA)和两种免疫球蛋白-抗人白细胞抗原(HLA)单克隆抗体和同种型对照IgG2a-用XenoLight CF770荧光染料标记,并用作NIR缀合的大分子探针,以研究多种形式的全身成像异种移植小鼠模型。在NIR大分子探针注射后24小时内,在皮下移植的BxPC-3(人类胰腺癌)细胞和HCT 116(结肠直肠癌)细胞中观察到NIR荧光信号,但该信号来自荧光素本身或结合NIR的小分子未观察到(甘氨酸)注射。通过皮下移植模型中N-共轭免疫球蛋白在T-HCT 116异种移植物中的定位(其中橙红色荧光蛋白tdTomato由HCT 116细胞稳定表达),证实了肿瘤靶向的准确性。但是,在皮下移植模型中,抗HLA抗体组和同型对照组之间的感兴趣区域的NIR信号强度没有显着差异。因此,体内肿瘤中的抗体蓄积是基于EPR效应。脾脏内注射T-HCT 116细胞产生的肝转移通过结合NIR的抗HLA探针清晰可见,但不通过tdTomato报告基因产生的橙红色荧光信号清晰可见。该结果证明了NIR探针在增强组织穿透性方面优于tdTomato报道蛋白。在另一个异种移植模型中,使用NIR偶联的大分子探针成功地可视化了患者来源的LC11-JCK(人非小细胞肺癌)异种移植物(PDX),而没有进行任何基因修饰。这些结果表明,NIR共轭的大分子,最好是抗HLA抗体探针,是使用全身成像在实验性转移模型中检测人类肿瘤的有价值的工具。

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