Jeffrey Segall's Lab

Sahai et al 2005 BMC Biotechnology

BMC Biotechnol. 2005 May 23;5:14.

Simultaneous imaging of GFP, CFP and collagen in tumors in vivo using multiphoton microscopy.

Sahai E, Wyckoff J, Philippar U, Segall JE, Gertler F, Condeelis J. 

Abstract 

BACKGROUND: The development of multiphoton laser scanning microscopy has greatly facilitated the imaging of living tissues. However, the use of genetically encoded fluorescent proteins to distinguish different cell types in living animals has not been described at single cell resolution using multiphoton microscopy. RESULTS: Here we describe a method for the simultaneous imaging, by multiphoton microscopy, of Green Fluorescent Protein, Cyan Fluorescent Protein and collagen in vivo in living tumors. This novel method enables: 1) the simultaneous visualization of overall cell shape and sub-cellular structures such as the plasma membrane or proteins of interest in cells inside living animals, 2) direct comparison of the behavior of single cells from different cell lines in the same microenvironment in vivo. CONCLUSION: Using this multi-fluor, multiphoton technique, we demonstrate that motility and metastatic differences between carcinoma cells of differing metastatic potential can be imaged in the same animal simultaneously at sub-cellular resolution. 

 

Additional File 1: Movie for figure 4A (avi. Format): Time-lapsed movie of high metastatic (MTLn3 overexpressing EGFR) CFP labeled cells (white) and low metastatic GFP labeled cells (green) crawling on collagen fibers (purple) in vivo. Objective used 20×. In general more CFP labeled cells move than GFP, consistent with EGFR overexpression enhancing motility in a cell automous fashion, not through changes in the tumor microenvironment. 

Additional File 3: Movie for figure 4E (avi. Format): Time-lapsed movie of high metastatic CFP labeled cells (white) and low metastatic GFP labeled cells (green) crawling on collagen fibers (purple) in vivo showing amoeboid characteristics and making rapid changes in direction. Objective used 40×.