Graduate School of Arts and Sciences, The University of Tokyo, 3-8-1 Komaba, Meguro-ku, Tokyo, 153-8902, Japan.
AMED-PRIME, Japan Agency for Medical Research and Development, Tokyo, Japan.
Sci Rep. 2018 Mar 5;8(1):3978. doi: 10.1038/s41598-018-22399-2.
The infiltration and proliferation of cancer cells in the secondary organs are of great interest, since they contribute to cancer metastasis. However, cancer cell dynamics in the secondary organs have not been elucidated at single-cell resolution. In the present study, we established an in vivo model using two-photon microscopy to observe how infiltrating cancer cells form assemblages from single T-cell lymphomas, EL4 cells, in the secondary organs. Using this model, after inoculation of EL4 cells in mice, we discovered that single EL4 cells infiltrated into the colon. In the early stage, sporadic elongated EL4 cells became lodged in small blood vessels. Real-time imaging revealed that, whereas more than 70% of EL4 cells did not move during a 1-hour observation, other EL4 cells irregularly moved even in small vessels and dynamically changed shape upon interacting with other cells. In the late stages, EL4 cells formed small nodules composed of several EL4 cells in blood vessels as well as crypts, suggesting the existence of diverse mechanisms of nodule formation. The present in vivo imaging system is instrumental to dissect cancer cell dynamics during metastasis in other organs at the single-cell level.
癌细胞在次级器官中的浸润和增殖是非常有趣的,因为它们有助于癌症转移。然而,次级器官中癌细胞的动力学还没有在单细胞分辨率下阐明。在本研究中,我们建立了一种使用双光子显微镜的体内模型,以观察浸润性癌细胞如何从单个 T 细胞淋巴瘤(EL4 细胞)在次级器官中形成聚集体。使用该模型,在将 EL4 细胞接种到小鼠后,我们发现单个 EL4 细胞浸润到结肠中。在早期,散在的拉长的 EL4 细胞被卡在小血管中。实时成像显示,虽然在 1 小时的观察中超过 70%的 EL4 细胞没有移动,但其他 EL4 细胞即使在小血管中也不规则地移动,并在与其他细胞相互作用时动态改变形状。在晚期,EL4 细胞在血管和隐窝中形成由几个 EL4 细胞组成的小结节,表明结节形成存在多种机制。本体内成像系统有助于在单细胞水平上解析转移过程中其他器官中癌细胞的动力学。