Robin Journot 🔬| 🎾
@robinjournot.bsky.social
330 followers 160 following 17 posts
PhD student in the Fre lab at @institutcurie.bsky.social Tissue morphogenesis & Fate specification in epithelia. Organoid and live imaging. Alumni AgroParisTech & ENS Ulm
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robinjournot.bsky.social
Our paper is on the cover of @cp-devcell.bsky.social . Image: embryonic murine salivary-gland explants stained for fate determinants; p63 (cyan) and HES1 (yellow). Thanks to everyone involved.
doi.org/10.1016/j.de...
robinjournot.bsky.social
Our paper is on the cover of @cp-devcell.bsky.social . Image: embryonic murine salivary-gland explants stained for fate determinants; p63 (cyan) and HES1 (yellow). Thanks to everyone involved.
doi.org/10.1016/j.de...
robinjournot.bsky.social
"Contractile fibroblasts form a transient niche for the branching mammary epithelium."
Now out: rdcu.be/eIIKD
A great contribution from Jakub Sumbal, showing how stromal cells, and diverse fibroblast subsets, regulate branching morphogenesis.
@sumbalovakoledova.bsky.social @frelab.bsky.social
robinjournot.bsky.social
From a FACS-contaminating cell population to a multi-organ project — learn the Behind the Story of our work on conserved signals in epithelial organogenesis 👉 www.sciencedirect.com/science/arti...
robinjournot.bsky.social
Yes! We think this mechanism goes way beyond glands. We're now exploring a broader range of tissues, stay tuned for what's coming next!
robinjournot.bsky.social
Great question! We haven’t inferred or directly measured mechanical forces yet, but in a follow-up project we’re actively investigating the mechanical component of the symmetry-breaking event. Very curious to see how it ties into YAP localization and happy to discuss more!
Reposted by Robin Journot 🔬| 🎾
bardinlab.bsky.social
Students (Master's/PhD), do not miss this fantastic Developmental Biology course of @sorbonne-universite.fr and @institutcurie.bsky.social - It is FREE and open to international students, however, room and board + travel are not included.

training.institut-curie.org/courses/deve...
robinjournot.bsky.social
Despite distinct germ layer origins and divergent adult functions, all 4 glands rely on the same YAP–Notch–p63 circuit to specify fate and pattern.
We propose an updated hourglass model where this conserved module acts as a developmental bottleneck in organogenesis.
robinjournot.bsky.social
In regeneration, we saw the same transitional state: YAP⁺p63⁺HES1⁺.
→ Developmental programs are reused for repair.
robinjournot.bsky.social
YAP acts then as a capacitor, counting the number of cell within the tissue before allowing cells to differentiate.
robinjournot.bsky.social
We found the key: YAP.
Initially nuclear in all cells, it becomes cytoplasmic in internal cells—coinciding with symmetry breaking and fate commitment. When we forced YAP activity, organoids didn’t break symmetry—cells stayed in a stem-like state, co-expressing p63 & HES1.
Same results in embryos!
robinjournot.bsky.social
But why do organoids stay homogeneous until ~13 cells?
Theoretical models say symmetry can break in 2 cells.
Here, an active mechanism seems to delay fate decisions early on.
robinjournot.bsky.social
We then asked: what regulates this decision?
Notch activation (in vivo or organoids) forced luminal fate.
Notch inhibition blocked it.
→ Notch is a gatekeeper of luminal identity.
We further demonstrated that symmetry breaking appeared through lateral inhibition.
robinjournot.bsky.social
We observed that fate segregation (K5 outside, K8 inside) happened not over time, but when organoids reached 13–21 cells.
→ This suggests size-dependent symmetry breaking drives fate commitment.
robinjournot.bsky.social
All 4 glands form 2-layered epithelia: K5⁺ basal cells on the outside, K8⁺ luminal facing the lumen.
But where does this structure come from during development? We sorted basal stem cells and grew organoids from all 4 tissues. They reactivated multipotency and gave rise to both cell types in vitro.
robinjournot.bsky.social
🧵Just out !
We reveal how 4 branched epithelia—mammary, lacrimal, salivary & prostate—use a conserved YAP–Notch–p63 circuit to self-organize during development & regeneration.
Here’s the story👇
authors.elsevier.com/c/1lM285Sx5g...
Work done in @frelab.bsky.social at ‪
@institutcurie.bsky.social
Reposted by Robin Journot 🔬| 🎾
embojournal.org
Notch1 activation in basal cells triggers a progressive basal-to-luminal cell-fate switch in the mouse mammary gland but also in adult cells of the lacrimal, salivary and prostatic glands
Silvia Fre and coworkers @frelab.bsky.social @institutcurie.bsky.social
www.embopress.org/doi/full/10....
Reposted by Robin Journot 🔬| 🎾
cschwayer.bsky.social
I am very excited to share our most recent work on how ‘Cell heterogeneity and fate bistability drive tissue patterning during intestinal regeneration’ ☺️ Thanks a lot to @silviabarbiero.bsky.social @davidbrueckner.bsky.social @priscaliberali.bsky.social
@ehannezo.bsky.social and all the co-authors!
robinjournot.bsky.social
A new platform, a new post!
Our #Stemcell #DevBio and #Regeneration
story by Silvia Fre's lab at InstitutCurie is on biorXiv.
Link: tinyurl.com/2uspcd3u

We reveal how 4 epithelia self-organize during embryonic development and regeneration.