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Intravital imaging of metastatic behavior through a mammary imaging window

Nature Methods volume 5, pages 10191021 (2008) | Download Citation

Abstract

We report a technique to evaluate the same tumor microenvironment over multiple intravital imaging sessions in living mice. We optically marked individual tumor cells expressing photoswitchable proteins in an orthotopic mammary carcinoma and followed them for extended periods through a mammary imaging window. We found that two distinct microenvironments in the same orthotopic mammary tumor affected differently the invasion and intravasation of tumor cells.

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Acknowledgements

This work was supported by US Department of Defense (BC061403 to D.K.), US National Institutes of Health (U54GM064346 to J.v.R.; CA100324 to J.C., J.E.S. and J.W.; U54CA126511 to J.C. and B.G.; and GM070358 and GM073913 to V.V.V.). We thank the staff of the Analytical Imaging Facility and D. Entenberg for help with microscopy, the immunohistochemistry facility for help with histology, M. Rottenkolber for help in fabrication of the imaging box, J. Pollard (Albert Einstein College of Medicine) for providing the F4/80 antibody, S. Garofalo for technical assistance, and members of the Condeelis, Segall, Cox and Verkhusha laboratories for discussions.

Author information

Author notes

    • Dmitriy Kedrin
    •  & Bojana Gligorijevic

    These authors contributed equally to this work.

Affiliations

  1. Department of Anatomy and Structural Biology, Albert Einstein College of Medicine of Yeshiva University, 1300 Morris Park Avenue, Bronx, New York 10461, USA.

    • Dmitriy Kedrin
    • , Bojana Gligorijevic
    • , Jeffrey Wyckoff
    • , Vladislav V Verkhusha
    • , John Condeelis
    • , Jeffrey E Segall
    •  & Jacco van Rheenen
  2. Gruss Lipper Biophotonics Center, Albert Einstein College of Medicine of Yeshiva University, 1300 Morris Park Avenue, Bronx, New York 10461, USA.

    • Bojana Gligorijevic
    • , Jeffrey Wyckoff
    • , Vladislav V Verkhusha
    • , John Condeelis
    •  & Jacco van Rheenen
  3. Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences and University Medical Center Utrecht, Uppsalalaan 8, 3584CT Utrecht, The Netherlands.

    • Jacco van Rheenen

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Corresponding authors

Correspondence to John Condeelis or Jeffrey E Segall or Jacco van Rheenen.

Supplementary information

PDF files

  1. 1.

    Supplementary Text and Figures

    Supplementary Figures 1–4, Supplementary Methods

Videos

  1. 1.

    Supplementary Movie 1

    Movie recorded through the ocular, at low magnification (10×). After focusing the field and checking for the flowing vessels in the green epifluorescence channel, the photoswitched area can be recognized in the red channel.

  2. 2.

    Supplementary Movie 2

    120-minute timelapse of a 250 × 250 µm area photoswitched inside the tumor. Notice the cells which move towards the fast flowing vessel. Non-photoswitched cells (green), photoswitched cells (red) and matrix (blue).

  3. 3.

    Supplementary Movie 3

    Z-stack of collagen (blue) and Dendra2-MTLn3 tumor cells (green and red) visualized in the live animal using a multiphoton microscope. The stepsize is 5µm.

  4. 4.

    Supplementary Movie 4

    10-minute timelapse of flowing vessels labeled using AlexaFluo647-10K (red, moving shadows are red blood cells) and Dendra2-MTLn3 tumor cells (green). Other channels were omitted for better contrast.

About this article

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DOI

https://doi.org/10.1038/nmeth.1269

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