Journal of Biomechanics
Volume 40, Issue 2 , Pages 335-344, 2007

Morphological analysis of tumor cell/endothelial cell interactions under shear flow

  • Roxana Chotard-Ghodsnia

      Affiliations

    • Laboratoire de Spectrométrie Physique, UMR 5588 (CNRS- Université Grenoble I) BP 87, 140 Rue de la Physique, Saint-Martin d’Hères 38402, France
    • Corresponding Author InformationCorresponding author: Laboratoire SPCTS, CNRS UMR 6638, ENSCI, 47-73 Avenue Albert Thomas, 87065 Limoges, France. Tel.: +33555452229; fax: +33555790998.
  • ,
  • Oualid Haddad

      Affiliations

    • INSERM, U578, Grenoble, France
    • Université Grenoble I, Groupe de Recherche sur le Cancer du Poumon, Institut Albert Bonniot, Grenoble, France
  • ,
  • Anne Leyrat

      Affiliations

    • Laboratoire de Spectrométrie Physique, UMR 5588 (CNRS- Université Grenoble I) BP 87, 140 Rue de la Physique, Saint-Martin d’Hères 38402, France
  • ,
  • Agnès Drochon

      Affiliations

    • Biomécanique et Génie Biomédical, UMR 6600 (CNRS- Université de Technologie de Compiègne), BP 20529, Compiègne Cedex 60205, France
  • ,
  • Claude Verdier

      Affiliations

    • Laboratoire de Spectrométrie Physique, UMR 5588 (CNRS- Université Grenoble I) BP 87, 140 Rue de la Physique, Saint-Martin d’Hères 38402, France
  • ,
  • Alain Duperray

      Affiliations

    • INSERM, U578, Grenoble, France
    • Université Grenoble I, Groupe de Recherche sur le Cancer du Poumon, Institut Albert Bonniot, Grenoble, France

Accepted 5 January 2006. published online 23 February 2006.

Abstract 

In the process of hematogenous cancer metastasis, tumor cells (TCs) must shed into the blood stream, survive in the blood circulation, migrate through the vascular endothelium (extravasation) and proliferate in the target organs. However, the precise mechanisms by which TCs penetrate the endothelial cell (EC) junctions remain one of the least understood aspects of TC extravasation. This question has generally been addressed under static conditions, despite the important role of flow induced mechanical stress on the circulating cell–endothelium interactions. Moreover, flow studies were generally focused on transient or firm adhesion steps of TC–EC interactions and did not consider TCs spreading or extravasation. In this paper, we used a parallel-plate flow chamber to investigate TC–EC interactions under flow conditions. An EC monolayer was cultured on the lower plate of the flow chamber to model the endothelial barrier. Circulating TCs were introduced into the flow channel under a well-defined flow field and TC cell shape changes on the EC monolayer were followed in vitro with live phase contrast and fluorescence microscopy. Two spreading patterns were observed: radial spreading which corresponds to TC extravasation, and axial spreading where TCs formed a mosaic TC–EC monolayer. By investigating the changes in area and minor/major aspect ratio, we have established a simple quantitative basis for comparing spreading modes under various shear stresses. Contrary to radial spreading, the extent of axial spreading was increased by shear stress.

Keywords: Metastasis, Extravasation, Endothelium, Flow, Cancer

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PII: S0021-9290(06)00009-1

doi:10.1016/j.jbiomech.2006.01.001

Journal of Biomechanics
Volume 40, Issue 2 , Pages 335-344, 2007