Premium
Real‐time observation of micrometastasis formation in the living mouse liver using a green fluorescent protein gene–tagged rat tongue carcinoma cell line
Author(s) -
Ito Seiji,
Nakanishi Hayao,
Ikehara Yuzuru,
Kato Tomoyuki,
Kasai Yasushi,
Ito Katsuki,
Akiyama Seiji,
Nakao Akimasa,
Tatematsu Masae
Publication year - 2001
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.1318
Subject(s) - micrometastasis , green fluorescent protein , pathology , biology , laminin , metastasis , extravasation , cell culture , microbiology and biotechnology , medicine , extracellular matrix , cancer , gene , biochemistry , genetics
Initial arrest, attachment, extravasation and subsequent extravascular growth of tumor cells in the secondary organs are believed to be crucial events for hematogenous metastasis, but the actual processes in living animals remain unclear. For the present study, we established green fluorescent protein (GFP)–expressing rat tongue carcinoma cell lines (RSC3) that permit real‐time analysis of micrometastasis formation in combination with intravital video microscopy (IVVM). With this system, GFP‐expressing metastatic (LM‐EGFP) and non‐metastatic (E2‐EGFP) cell lines could be visualized at the cellular level in live mice for more than 1 month. Real‐time IVVM analysis of liver metastases after intraportal injection of cells via a mesenteric vein revealed that both LM‐EGFP and E2‐EGFP tumor cells arrest similarly in sinusoidal vessels near terminal portal venules within 0.4 sec, during which time no evidence of a “rolling”‐like movement along endothelial cell surfaces was observed. Quantitative analysis of GFP‐positive foci showed that E2‐EGFP cells were completely sheared from the liver sinusoid within 3 days, with no solitary dormant cells, whereas a substantial number of LM‐EGFP cells remained in the liver, probably due to stable attachment to the sinusoidal wall. Confocal laser scanning microscopic study in combination with laminin immunohistochemistry revealed that only LM‐EGFP cells started growth at 3 to 4 days after inoculation and that most of the growing foci were surrounded by subsinusoidal basement membrane. Our results suggest that micrometastasis formation by LM‐EGFP cells consists of initial tumor cell arrest due to size constraints of the vessel, stable attachment to subsinusoidal basement membrane and subsequent intravascular growth before extravasation. The difference in metastatic potential between the 2 lines may reside in their capacity to attach stably to the vessel wall rather than their potential for initial cell arrest or subsequent growth. The system used in the present study may be a powerful tool for analyzing targets for various anti‐metastatic agents in the sequential process of metastasis. © 2001 Wiley‐Liss, Inc.