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双色荧光成像可区分肿瘤细胞与诱导生成的宿主血管生成血管及基质细胞。

Dual-color fluorescence imaging distinguishes tumor cells from induced host angiogenic vessels and stromal cells.

作者信息

Yang Meng, Li Lingna, Jiang Ping, Moossa A R, Penman Sheldon, Hoffman Robert M

机构信息

AntiCancer, 7917 Ostrow Street, San Diego, CA 92111, USA.

出版信息

Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14259-62. doi: 10.1073/pnas.2436101100. Epub 2003 Nov 12.

Abstract

We have developed a simple yet powerful technique for delineating the morphological events of tumor-induced angiogenesis and other tumor-induced host processes with dual-color fluorescence. The method clearly images implanted tumors and adjacent stroma, distinguishing unambiguously the host and tumor-specific components of the malignancy. The dual-color fluorescence imaging is effected by using red fluorescent protein (RFP)-expressing tumors growing in GFP-expressing transgenic mice. This model shows with great clarity the details of the tumor-stroma interaction, especially tumor-induced angiogenesis and tumor-infiltrating lymphocytes. The GFP-expressing tumor vasculature, both nascent and mature, could be readily distinguished interacting with the RFP-expressing tumor cells. GFP-expressing dendritic cells were observed contacting RFP-expressing tumor cells with their dendrites. GFP-expressing macrophages were observed engulfing RFP-expressing cancer cells. GFP lymphocytes were seen surrounding cells of the RFP tumor, which eventually regressed. Dual-color fluorescence imaging visualizes the tumor-host interaction by whole-body imaging and at the cellular level in fresh tissues, dramatically expanding previous studies in fixed and stained preparations.

摘要

我们已经开发出一种简单却强大的技术,用于通过双色荧光描绘肿瘤诱导的血管生成及其他肿瘤诱导的宿主过程中的形态学事件。该方法能清晰地对植入的肿瘤和邻近基质进行成像,明确区分恶性肿瘤中宿主和肿瘤特异性成分。双色荧光成像通过在表达绿色荧光蛋白(GFP)的转基因小鼠体内生长的表达红色荧光蛋白(RFP)的肿瘤来实现。该模型非常清晰地展示了肿瘤-基质相互作用的细节,尤其是肿瘤诱导的血管生成和肿瘤浸润淋巴细胞。表达GFP的新生和成熟肿瘤血管系统能够很容易地与表达RFP的肿瘤细胞区分开来。观察到表达GFP的树突状细胞用其树突接触表达RFP的肿瘤细胞。观察到表达GFP的巨噬细胞吞噬表达RFP的癌细胞。看到表达GFP的淋巴细胞围绕着表达RFP的肿瘤细胞,这些肿瘤细胞最终消退。双色荧光成像通过全身成像以及在新鲜组织的细胞水平上可视化肿瘤-宿主相互作用,极大地扩展了以往在固定和染色制剂方面的研究。

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