Hayashi Katsuhiro, Jiang Ping, Yamauchi Kensuke, Yamamoto Norio, Tsuchiya Hiroyuki, Tomita Katsuro, Moossa A R, Bouvet Michael, Hoffman Robert M
AntiCancer Inc, San Diego, CA 92111-3604, USA.
Cancer Res. 2007 Sep 1;67(17):8223-8. doi: 10.1158/0008-5472.CAN-07-1237.
In the present report, we show real-time imaging of cancer cell trafficking in lymphatic vessels. Cancer cells labeled with both green fluorescent protein (GFP) in the nucleus and red fluorescent protein (RFP) in the cytoplasm or with GFP only or RFP only were injected into the inguinal lymph node of nude mice. The labeled cancer cells trafficked through lymphatic vessels where they were imaged via a skin flap in real time at the cellular level until they entered the axillary lymph node. The bright fluorescence of the cancer cells and the real-time microscopic imaging capability of the Olympus OV100 small-animal imaging system enabled imaging of the trafficking cancer cells in the lymphatics. Using this imaging strategy, two different cancer cell lines, one expressing GFP and the other expressing RFP, were simultaneously injected in the inguinal lymph node. Fluorescence imaging readily distinguished the two color-coded cell lines and their different abilities to survive in the lymphatic system. Using this imaging technology, we also investigated the role of pressure on tumor-cell shedding into lymphatic vessels. Pressure was generated by placing 25- and 250-g weights for 10 s on the bottom surface of a tumor-bearing footpad. Tumor cell fragments, single cells, and emboli shed from the footpad tumor were easily distinguished with the labeled cells and OV100 imaging system. Increasing pressure on the tumor increased the numbers of shed cells, fragments, and emboli. Pressure also deformed the shed emboli, increasing their maximum major axis. Imaging lymphatic trafficking of cancer cells can reveal critical steps of lymph node metastasis.
在本报告中,我们展示了癌细胞在淋巴管中迁移的实时成像。将细胞核中标记有绿色荧光蛋白(GFP)且细胞质中标记有红色荧光蛋白(RFP)的癌细胞,或仅标记有GFP或仅标记有RFP的癌细胞,注射到裸鼠的腹股沟淋巴结中。标记的癌细胞通过淋巴管迁移,在那里它们通过皮瓣在细胞水平上进行实时成像,直到进入腋窝淋巴结。癌细胞的明亮荧光以及奥林巴斯OV100小动物成像系统的实时显微成像能力,使得能够对淋巴管中迁移的癌细胞进行成像。使用这种成像策略,将两种不同的癌细胞系,一种表达GFP,另一种表达RFP,同时注射到腹股沟淋巴结中。荧光成像很容易区分这两种颜色编码的细胞系以及它们在淋巴系统中不同的存活能力。使用这种成像技术,我们还研究了压力对肿瘤细胞脱落进入淋巴管的作用。通过在荷瘤脚垫的底面放置25克和250克的重物10秒来产生压力。从脚垫肿瘤脱落的肿瘤细胞碎片、单细胞和栓子,通过标记细胞和OV100成像系统很容易区分。增加对肿瘤的压力会增加脱落细胞、碎片和栓子的数量。压力还会使脱落的栓子变形,增加其最大长轴。对癌细胞淋巴迁移进行成像可以揭示淋巴结转移的关键步骤。