Pichaud Lab
Cell biology of tissue architecture and physiology
Our research aims to unravel one of the greatest mysteries in biology and medicine – how different cell types interact to generate functional organs during development. Our focus is on epithelial tissues, the building blocks of most organs. These tissues perform critical functions such as selective exchange of gas, nutrients, and waste products, and provide structural support. They are masterfully shaped to suit each organ's unique needs, from stratified layers for protection, like the skin, to tubular networks for increased surface area, such as in the intestine. Generating the intricate three-dimensional epithelial structures that support our organs requires cells to coordinate their movement and changes in their shape. Our research aims to uncover the mechanisms and molecular pathways behind this coordination. To study this, we use a multidisciplinary approach that combines genetic, molecular and optogenetic methods in vivo, mammalian cell cultures, mathematical modelling, and state-of-the-art imaging. Our favourite model system is the genetically amenable eye of Drosophila melanogaster, which allows us to perturb gene expression and protein function in individual cell types while studying the consequences in a developing living epithelium. By understanding how cells work together to induce three-dimensional tissue organisation during organ development, we hope to gain insights into how abnormal epithelial tissues architecture might arise in development and homeostasis, causing diseases such as cancer, for example. The goal of our research is to contribute to our understanding of the pathways that promote epithelial tissue development and to help advancing our ability to diagnose, treat, and prevent epithelial diseases.
Principal funders
Franck Pichaud (PI)
Rhian Walther (Investigator scientist, MRC)
Adam Wells (Investigator scientist, MRC)
Courtney Lancaster (PhD student, Optical Biology, Wellcome)
Hadjar Sebaa (PhD student, LiDo)
Xiyeu Hu (Master student, Cell Biology)
Prof Jennifer Curtiss (Visiting Scientist, University New Mexico, USA)
Cytoskeleton and cell cortex
Basement membranes
Polarity and cell shape
Cell-cell interactions
Membrane trafficking
Light microscopy
Translational research
Bioinformatics
Super-resolution microscopy
Electron microscopy
Computational modelling
Selected publications
Walther RF, et al (2024). A Dystroglycan–Laminin–Integrin axis controls cell basal geometry remodeling in the developing Drosophila retina. Plos Biology Sep 3;22(9):e3002783
Nunes de Almeida F, et al (2019). Cdc42 defines apical identity and regulates epithelial morphogenesis by promoting apical recruitment of Par6-aPKC and Crumbs. Development 146: dev175497.
Walther RF, et al (2018). Rap1, Canoe and Mbt cooperate with Bazooka to promote Zonula Adherens assembly in the fly photoreceptor. Journal of Cell Science 131, jcs207779.
Zihni C, et al (2017). An apical MRCK-driven morphogenetic pathway controls epithelial polarity. Nature Cell Biology 19, 1049-1060.
Walther RF, et al (2016). Pak4 Is Required during Epithelial Polarity Remodeling through Regulating AJ Stability and Bazooka Retention at the ZA. Cell Reports, 15 (1), 45-53. doi:10.1016/j.celrep.2016.03.014