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Quantitative Analysis of Melanocyte Migration in vitroBased on Automated Cell Tracking under Phase Contrast Microscopy Considering theCombined Influence of Cell Division and Cell-Matrix Interactions

Published online by Cambridge University Press:  03 February 2010

V. Letort ,
S. Fouliard ,
G. Letort ,
I. Adanja ,
M. Kumasaka ,
S. Gallagher ,
O. Debeir ,
L. Larue  and
F. Xavier
V. Letort
Affiliation:
Laboratory of Applied Mathematics, Ecole Centrale Paris, F-92295 Chatenay-Malabry, France
S. Fouliard
Affiliation:
Laboratory of Applied Mathematics, Ecole Centrale Paris, F-92295 Chatenay-Malabry, France
G. Letort
Affiliation:
Laboratory of Applied Mathematics, Ecole Centrale Paris, F-92295 Chatenay-Malabry, France
I. Adanja
Affiliation:
Laboratory of Image Synthesis and Analysis (LISA), Faculty of Applied Sciences, Universite Libre de Bruxelles, 1050 Brussels, Belgium
M. Kumasaka
Affiliation:
Institut Curie, Centre Recherche, Developmental Genetics of Melanocytes, F-91405 Orsay, France CNRS UMR146, F-91405 Orsay, France
S. Gallagher
Affiliation:
Institut Curie, Centre Recherche, Developmental Genetics of Melanocytes, F-91405 Orsay, France CNRS UMR146, F-91405 Orsay, France
O. Debeir
Affiliation:
Laboratory of Image Synthesis and Analysis (LISA), Faculty of Applied Sciences, Universite Libre de Bruxelles, 1050 Brussels, Belgium
L. Larue
Affiliation:
Institut Curie, Centre Recherche, Developmental Genetics of Melanocytes, F-91405 Orsay, France CNRS UMR146, F-91405 Orsay, France
F. Xavier*
Affiliation:
Laboratory of Applied Mathematics, Ecole Centrale Paris, F-92295 Chatenay-Malabry, France
*
* Corresponding author. E-mail:francoise.xavier@ecp.fr
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Abstract

The aim of this study was to describe and analyze the regulation and spatio-temporaldynamics of melanocyte migration in vitro and its coupling to celldivision and interaction with the matrix. The melanocyte lineage is particularlyinteresting because it is involved in both embryonic development andoncogenesis/metastasis (melanoma). Biological experiments were performed on two melanocytecell lines established from wild-type and β-catenin-transgenic mice(bcat*). The multi-functional β-catenin molecule is known to be able toregulate the transcription of various genes involved in cell proliferation and migration,particularly in the melanocyte lineage. We also investigated fibronectin, anextra-cellular matrix protein that binds integrins, thereby providing adhesion points forcells and encouraging migration. As the migration of individual cells were followed,automated methods were required for processing the large amount of data generated by thetime-lapse video-microscopy. A model-based approach for automated cell tracking wasevaluated on a sample by comparison with manual tracking. This method was found reliablein studying overall cell behaviour. Its application to all the observed sequences providedinsight into the factors affecting melanocyte migration in vitro:melanocytes of mutated form of β-catenin showed higher division rates andno contact inhibition of growth was induced by the resulting increase in cell density.However, cell density limited the amplitude of cell displacements, although their motilitywas less affected. The high fibronectin concentration bound to substratum promoted cellmigration and motility, the effect being more intense for wild-type cells than for cellswith β-catenin over-expression. During the division process, cellmigration speed increased rapidly then decreased slowly. Analyses of such data is expectedto lead both to biological answers and to a framework for a better modeling processes inthe future.

Keywords

melanocytesautomated cell trackingvideo microscopycell migrationcell divisioncell-matrix interactionβ-cateninfibronectin.
Type
Research Article
Information
Mathematical Modelling of Natural Phenomena , Volume 5 , Issue 1: Cell migration , 2010 , pp. 4 - 33
Copyright
© EDP Sciences, 2010

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