Aurélien Villedieu
@aurelienvilledieu.bsky.social
100 followers 150 following 14 posts
Postdoc in Jérôme Gros's team | Former PhD student in Yohanns Bellaïche's team | Multi-scale study of tissue morphogenesis | Live-imaging and quantitative biology
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Reposted by Aurélien Villedieu
denisduboule.bsky.social
Out today. 🙏 again to everyone for this wonderful piece of work, in particular to Aurelie @aurhin.bsky.social Chase @chasebolt.bsky.social and Brent @homeobox.bsky.social. 🙏 also to the Harris lab @fish4walking.bsky.social and @neilshubin.bsky.social @biology-unige.bsky.social @college-de-france.fr
Reposted by Aurélien Villedieu
paveltomancak.bsky.social
We are all super happy and proud to see our work on the function and evolution of the #cephalic #furrow published in @nature.com. Let me say a few things about the background and history of this work on the #Evolution_of_Morphogenesis (1/12)
Reposted by Aurélien Villedieu
jamesbriscoe.bsky.social
Our latest: We developed a chemo-optogenetic system for precise spatiotemporal control of morphogen production. Using dual light + small molecule control of Sonic Hedgehog production, we recapitulated neural tube patterning in vitro & measured spread of Shh

🧵

www.sciencedirect.com/science/arti...
Investigating morphogen and patterning dynamics with optogenetic control of morphogen production
Morphogen gradients provide the patterning cues that instruct cell fate decisions during development. Here, we establish an optogenetic system for the…
www.sciencedirect.com
Reposted by Aurélien Villedieu
michalis-averof.bsky.social
Latest paper elifesciences.org/articles/107... closes an important cycle in our efforts to study regeneration: week-long recordings allow us to observe the behaviour of cells during the entire course of regeneration in a crustacean leg – bright objects in movie are fluorescent nuclei of cells. 1/6
Reposted by Aurélien Villedieu
anaisbailles.bsky.social
Very happy that the first article from my postdoc work in the Tomancak lab is now published @PNAS! www.pnas.org/doi/10.1073/.... We studied the self-organization of actin in aggregates made from Hydra cells. Thread below (1/9)
Reposted by Aurélien Villedieu
epimechfc.bsky.social
If you’ve been following this account closely, you might already know methods to probe mechanics in vitro, but what about in live embryos?

I’m @amichaut.bsky.social, and I’m going to share a few great papers on this aspect of #EpithelialMechanics.
Reposted by Aurélien Villedieu
juliapfanzelter.bsky.social
Here is what I have been up to in the lab of @stephangrill.bsky.social together with @neipel.bsky.social and many others.
Intrigued by avian left right symmetry breaking we found that a tissue-scale active torque drives chiral flow and requires mechanical coupling to the underlying tissue.
aurelienvilledieu.bsky.social
🚨 A very interesting conference on gastrulation coming up soon 🚨 Don't miss the chance to interact with these renowned speakers! Early bird deadline: July 15th
jeromegros.bsky.social
Registration is now open!

Gastrulation Reloaded: Developing, engineering & evolving the body plan

📅 October 14–17, 2025
📍 Paris, France
🗓️ Abstract & early bird deadline: July 15, 2025

www.gastrulation-reloaded.conferences-pasteur.org/home

Exceptional lineup of speakers & many selected talks
Reposted by Aurélien Villedieu
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 Aurélien Villedieu
deniskrndija.bsky.social
🥳 Thrilled to share our lab's first preprint, led by our talented postdoc Justine Creff! 👩🏻‍🔬 We tackled a fundamental question: how the epithelium withstands mechanical stress at the interface of cells with distinct geometries and mechanics, such as enterocytes (E) and goblet cells (G) (1/9)
Reposted by Aurélien Villedieu
tomcumming.bsky.social
The effector caspases drive cell death, but their activation can often be survived, so how do cells make this decision? Our new preprint from @levayerr.bsky.social shows that instantaneous caspase activity is important, but past activation has a key role to play!

www.biorxiv.org/content/10.1...
aurelienvilledieu.bsky.social
Our results thus show that primitive streak formation is induced by NODAL activation in the posterior hypoblast. The movement of the hypoblast (which is a counter-rotating movement) is a consequence of primitive streak formation – and not a cause of it, as previously thought.
aurelienvilledieu.bsky.social
Finally, we investigated whether the anterior hypoblast could inhibit primitive streak formation, as previously thought. By grafting the anterior hypoblast onto the forming primitive streak, we could show that it does not. On the contrary, the grafted hypoblast starts to express NODAL.
aurelienvilledieu.bsky.social
In this movie, you can for example see that the full ablation of the hypoblast completely inhibits primitive streak formation, while a partial ablation that leaves a piece of posterior hypoblast on each side leads to the formation of two embryonic axes (forming conjoined twins).
aurelienvilledieu.bsky.social
Using functional analyses and tissue-recombination experiments, we confirmed that the posterior hypoblast is indeed the inducer of primitive streak formation through NODAL signaling activation.
aurelienvilledieu.bsky.social
Using HCR-RNA-FISH, we observed that the expression of NODAL, a master activator of primitive streak formation, initiates in the posterior hypoblast and then spreads to the entire posterior blastoderm.
aurelienvilledieu.bsky.social
The hypoblast thus remains in constant contact with the epiblast, which is incompatible with the idea that its movement controls primitive streak formation by locally lifting NODAL inhibition. This contradiction led us to reinvestigate the molecular mechanisms underlying primitive streak formation.
aurelienvilledieu.bsky.social
By intercalating a porous filter between the epiblast and the hypoblast, we further showed that the hypoblast requires physical contact with the epiblast to achieve counter-rotating flows. Thus, forces generated in the epiblast propagate by mechanical coupling to the hypoblast, setting it in motion.
aurelienvilledieu.bsky.social
By generating a two-color chimera, we observed that the counter-rotating flows of the epiblast and hypoblast are highly synchronized. As a result, the hypoblast and epiblast move very little in relation to each other.
aurelienvilledieu.bsky.social
We have adapted live-imaging techniques previously used to characterize tissue flows in the avian epiblast to describe, this time, tissue flows in the hypoblast. This allowed us to discover that, like the epiblast, the hypoblast exhibits counter-rotating flows (also known as Polonaise movements).