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Study of cell shape changes during embryogenesis: application to the sea urchin (M/F)

This offer is available in the following languages:
- Français-- Anglais

Date Limite Candidature : mercredi 27 août 2025 23:59:00 heure de Paris

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Informations générales

Intitulé de l'offre : Study of cell shape changes during embryogenesis: application to the sea urchin (M/F) (H/F)
Référence : UMR7271-MAGRIC-006
Nombre de Postes : 1
Lieu de travail : VALBONNE
Date de publication : mercredi 6 août 2025
Type de contrat : CDD Doctorant
Durée du contrat : 36 mois
Date de début de la thèse : 1 octobre 2025
Quotité de travail : Complet
Rémunération : 2200 gross monthly
Section(s) CN : 07 - Sciences de l'information : traitements, systèmes intégrés matériel-logiciel, robots, commandes, images, contenus, interactions, signaux et langues

Description du sujet de thèse

Study of cell shape changes during embryogenesis: application to the sea urchin.

Activities :
- Numerical experiments
- Code writing
- Results computation
- Results presentation
- Article writing

Skills :
- Knowledge in image processing, preferably 3D
- Computer skills: programming (python), image processing/graphics libraries
- Written and spoken english

Experience :
Master in computer sciences or applied mathematics (with interest in biology) or in bioinformatics (with interest in computer sciences).

Contexte de travail

This position is available within the Morpheme team - SIS Department of the i3S / UMR7271 Laboratory in Sophia Antipolis. The Laboratory for Computer Science, Signals and Systems at Sophia Antipolis (i3S), set up in 1989, conducts research in computer science. With a staff of nearly 300, including professors and researchers from the Université Côte d'Azur, CNRS and Inria researchers, administrative and technical staff, doctoral students and trainees, it is one of the largest public laboratories on the Côte d'Azur and was one of the first to be established in the Sophia Antipolis technology park.
Developmental biology aims to better understand the morphogenesis. Image-based studies represent a method of choice therefore. From now on, microscopy techniques enable acquisition of temporal sequences of 3D images with a spatio-temporal resolution good enough to follow the embryo or organ development at sub-cellular scale [1]. While each still image allows to individualize each cell, the study of the temporal series may allow to extract the cell lineage and thus to follow one cell during the development and to recognize the cell division.
The acquisition of 3D+t series results in huge quantities of data. Obviously, manual analysis of such number of images is not possible and sophisticated image analysis tools have been developed in the recent years for this particular goal [2]. A first study [3] has already permits to segment the cells and to track them along time, each acquisition being made of more than a hundred of 3D images. This approach has been successfully adapted to temporal series of sea urchin embryo images [4] in joint research between the Morpheme team and Rauzi's team that has resulted in the segmentation of several 3D+t microscopic acquisitions of developing sea urchin embryos. That has allowed a quantified morphometric of the embryo cells all along the acquisition. Such results give access to a detailed morphometric analysis of single cell shapes.
We are interested in the gastrulation phase of the sea urchin embryo. During this phase, a cavity appears which implies mechanical constraints at the cellular level. Such constraints also cause specific cell shape evolution. The goal of this thesis is to identify the 3D morphological and topological modifications at the cellular level that correlates with the gastrulation. More precisely, the 3D cell shape evolution will be characterized at an individual level and the cell population exhibiting similar evolution, either within a single embryo and within a population of embryos, will be further analysed to characterize a global behaviour. In a first steps, the so-called bottle cells, where the ratio between basal and apical surfaces rapidly evolves, will be investigated, as well as the cell intercalation. Classification/clustering techniques will help to characterize sub-populations of cells in the developing embryos.

Bibliography
[1] PJ Keller, “Imaging Morphogenesis: Technological Advances and Biological Insights,” Science, vol. 340, no. 6137, pp. 1234168+, June 2013.
[2] R Fernandez, P Das, V Mirabet, E Moscardi, J Traas, JL Verdeil, G Malandain, and C Godin, “Imaging plant growth in 4-d: robust tissue reconstruction and lineaging at cell resolution,”Nat Meth, vol. 7, pp. 547–553, 2010.
[3] Guignard, L., Fiuza, U.-M., Leggio, B., Laussu, J., Faure, E., Michelin, G., Biasuz, K., Hufnagel, L., Malandain, G., Godin, C., and Lemaire, P. (2020). Contact-area dependent cell communications and the morphological invariance of ascidian embryogenesis. Science, accepted for publication.
[4] Moullet, A. (2020) “Automated segmentation of sea urchin embryos”, Ms thesis.

Le poste se situe dans un secteur relevant de la protection du potentiel scientifique et technique (PPST), et nécessite donc, conformément à la réglementation, que votre arrivée soit autorisée par l'autorité compétente du MESR.

Contraintes et risques

None