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      <div class="TdmEntry">Overall Objectives<ul><li><a href="./uid3.html">Glossary</a></li><li><a href="./uid4.html">Scientific context and motivations</a></li><li><a href="./uid5.html">Objectives in cell imaging</a></li><li><a href="./uid9.html">Main challenges in image processing for multimodal and multidimensional microscopy</a></li><li><a href="./uid10.html">Organization and collaborations</a></li></ul></div>
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      <div class="TdmEntry">Application Domains<ul><li><a href="uid18.html&#10;&#9;&#9;  ">Modeling and analysis of membrane transport and molecule trafficking at the single cell scale</a></li><li class="tdmActPage"><a href="uid24.html&#10;&#9;&#9;  ">Imaging and analysis of cytokskeleton dynamics during cell migration</a></li></ul></div>
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	    2016</a> | <a href="http://www.inria.fr/en/teams/serpico">Presentation of the Project-Team SERPICO</a> | <a href="http://serpico.rennes.inria.fr/">SERPICO Web Site
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        <h2>Section: 
      Application Domains</h2>
        <h3 class="titre3">Imaging and analysis of cytokskeleton dynamics during cell migration</h3>
        <p>The ability to migrate in space is among the most fundamental functions of eukaryotic cells and thus is
one of the best-studied phenomena in biology. During embryonic development, cell movements result
in a massive reorganization of the embryo, from a simple spherical ball of cells into a multi-layered
organism; many of the cells at or near the surface of the embryo move to a new, more interior location.
Moreover, inadequate or inappropriate migration of immune cells is also critically important for the
delivery of protective immune responses to tissues and for wound healing. Finally, cell migration may
facilitate the dissemination of tumor cells in blood and organs and eventually the formation of
secondary tumors and metastases.</p>
        <p>It has been established that the cytoskeleton, composed of actin filaments, microtubules and
intermediate filaments (elongated structures with a diameter of a few dozens of nanometers), is
essential for several cell mechanisms, including cell migration, cell division and molecule trafficking:</p>
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            <p class="notaparagraph"><a name="uid25"> </a>i/ the actin filaments promote cell protrusion, adhesion and retraction;</p>
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            <p class="notaparagraph"><a name="uid26"> </a>ii/ the microtubules are the support of molecule traffic and cell polarization;</p>
          </li>
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            <p class="notaparagraph"><a name="uid27"> </a>iii/ the intermediate filaments are hypothesized to control microtubule organization.</p>
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        <p>Nevertheless, the mechanical and chemical states of migrating cells under various external conditions remain largely unknown. In the last decade, high-resolution microscopy methods led to the discovery of novel
aspects of cell migration. Most approaches and models are limited to migration in 2D, justified by the
flatness of the cell-motile mechanisms. However, the mechanical patterns that govern migration in 2D
models are often not essential for efficient migration in 3D. Accordingly, recent very challenging 3D
models of cells moving on flat surfaces have begun to emerge. The key challenge, however, is to
understand how a 3D motile cell crawls through the 3D extracellular matrix.</p>
        <p>The objective of <span class="smallcap">serpico </span> is to develop high-end signal processing and computer vision tools
to unfold the dynamical coordination of microtubules, actin filaments and intermediate filaments in 3D, involved in cell migration, cell division and molecule trafficking.</p>
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