CV – Research – Lab members – Publications
Dr. Agathe Chaigne
Cell Biology, Neurobiology and Biophysics,
Faculty of Science, Utrecht University
Kruytgebouw, room N501
Padualaan 8, 3584 CH Utrecht, The Netherlands
Agathe Chaigne studied cell biology and developmental biology in Ecole Normale Supérieure and Université Pierre et Marie Curie, in Paris, France. She obtained a teaching degree in 2010, her masters in 2011 and her PhD in 2014 studying the role of cortex tension in spindle positioning of the mouse oocyte, under the supervision of Marie-Hélène Verlhac and Marie-Emilie Terret. She did her postdoc in the lab of Ewa Paluch in University College London and Cambridge University, in collaboration with Kevin Chalut and Edouard Hannezo as an EMBO fellow then a sir Henry Wellcome postdoctoral fellow. During that time, she investigated the role of cell division in cell fate transitions using mouse embryonic stem cells as a model system. She started her own lab at the department of Cell Biology, Neurobiology and Biophysics in January 2022.
Cell division is crucial for development: it allows an increase in the number of cells, while also being important for cell fate transitions. Indeed, cell division can produce cells that are different from the mother cells, or different from each other in the case of asymmetric division.
We aim at understanding how the fundamental mechanisms of cell division can control fate transitions, with a developmental and evolutionary perspective. We are particularly interested in the last step of cell division, abscission, which is the final cut between the sister cells. While the textbook picture of cell division describes abscission following shortly cytokinesis, some cells do not perform abscission but instead remain connected by cytoplasmic bridges for extended periods of time. We are interested in the mechanisms of formation, maintenance, and roles of the cytoplasmic bridges (Figures created using Biorender.com).
Using live-cell imaging, comparative approaches, proteomics, and manipulation of abscission, we are currently focusing on two specific questions:
- How are bridges maintained and what are their roles in early development? To answer this question, we are using mouse embryonic stem cells as a model system. Pluripotent stem cells maintain long-lived bridges and dismantling of bridges through accelerated abscission is crucial to exit from naïve pluripotency.
- What is the conservation of bridge maintenance across the tree of life, and what role did in play in the evolution of animal multicellularity? To address this question, we plan on comparing bridges in different species, in particular in choanoflagellates, the closest living relatives to animals.
Chaigne, A., Smith, M. B., Lopez Cavestany, R., Hannezo, E., Chalut, K. J. and Paluch, E. K. (2021). Three-dimensional geometry controls division symmetry in stem cell colonies. Journal of Cell Science 134, jcs255018.
Chaigne, A., Labouesse, C., White, I.J., Agnew, M., Hannezo, E., Chalut, K.J., and Paluch, E.K. (2020). Abscission Couples Cell Division to Embryonic Stem Cell Fate. Developmental Cell.
Dimitracopoulos, A.*, Srivastava, P*, Chaigne, A., Win, Z., Shlomovitz, R., Lancaster, O.M., Le Berre, M., Piel, M., Salbreux, G., Baum, B. Mechanochemical crosstalk produces intrinsic patterning of the cell cortex to orient the mitotic spindle. Current Biology.
Bennabi, I., Crozet, F., Nikalayevich, E., Chaigne, A., Letort, G., Manil-Ségalen, M., Campillo, C., Cadart, C., Othmani, A., Attia, R., et al. (2020). Artificially decreasing cortical tension generates aneuploidy in mouse oocytes. Nature Communications 11.
Smith, M. B., Chaigne, A. & Paluch, E. K. (2016). An active contour ImageJ plugin to monitor daughter cell size in 3D during cytokinesis. In Methods in Cell Biology.
Chaigne, A., Campillo, C., Voituriez, R., Gov, N.S., Sykes, C., Verlhac, M.-H., and Terret, M.-E. (2016). F-actin mechanics control spindle centring in the mouse zygote. Nat. Commun. 7, 10253.
Chaigne, A., Campillo, C., Gov, N.S., Voituriez, R., Sykes, C., Verlhac, M.H., and Terret, M.E. (2015). A narrow window of cortical tension guides asymmetric spindle positioning in the mouse oocyte. Nat. Commun. 6, 6027.
Chaigne, A., Campillo, C., Gov, N.S.*, Voituriez, R.*, Azoury, J., Umaña-Diaz, C., Almonacid, M., Queguiner, I., Nassoy, P., Sykes, C., Verlhac, M.-H., Terret, M.-E., 2013. A soft cortex is essential for asymmetric spindle positioning in mouse oocytes. Nat. Cell Biol. 15, 958–966.
Reviews & Protocoles
Carla Mulas, Agathe Chaigne, Austin Smith, Kevin J. Chalut; Cell state transitions: definitions and challenges. Development 15 October 2021; 148 (20): dev199950. doi: https://doi.org/10.1242/dev.199950
Chaigne, A. In Vitro Fertilization of Mouse Oocyte. Methods Mol. Biol. 1818, 37–42 (2018).
Chaigne, A., Terret, M.-E. & Verlhac, M.-H. Asymmetries and Symmetries in the Mouse Oocyte and Zygote. in Asymmetric Cell Division in Development, Differentiation and Cancer (eds. Tassan, J.-P. & Kubiak, J. Z.) 61, 285–299 (Springer International Publishing, 2017).
Chaigne, A., Verlhac, M.-H., Terret, M.-E., 2014. Ramollir le cortex: Un prérequis à l’asymétrie de la division ovocytaire. médecine/sciences 30, 18–21.
Terret, M.-E., Chaigne, A., Verlhac, M.-H., 2013. Mouse oocyte, a paradigm of cancer cell. Cell Cycle 12, 0–6.
Chaigne, A., Verlhac, M.-H. and Terret, M.-E. 2012. Spindle positioning in mammalian oocytes. Experimental Cell Research 318, 1442–1447.