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🧠 Join us @uzh-ch.bsky.social ! We are a new lab looking for PhDs, Postdocs & Master’s students interested in studying how human neural systems emerge & go awry using brain organoids, light-sheet imaging & genomics. πŸš€ Deadline for LSZGS 1st Nov! www.lifescience-graduateschool.uzh.ch/en.html.
Check out our latest preprint on the cellular mechanical basis of Voronoi tessellations in epithelia! This biophysics study is inspired by disordered tessellations observed in zebrafish hearts πŸ€“πŸŸπŸ’™ #SulaimaanLim #ChiuFanLeeLab arxiv.org/html/2512.13...
Endocardial cells in the valve-forming region undergo a significant volume reduction during early heart development.
Enjoy! πŸ₯‚ #CardiacDevelopment #Mechanobiology #DevelopmentalBiology #Morphogenesis #Piezo1 #Aquaporins #Zebrafish
A huge thank you to all our fantastic collaborators (@kkalyviotis.bsky.social, Shuyi Feng, Antoine Sanchez, Igor Kondrychyn, Moe Fukumoto, Xiangbin Pan, Thomas Juan, @stainierlab.bsky.social, @pantazislab.bsky.social, @phnglab.bsky.social) and @imperialcollegeldn.bsky.social!
πŸ’§ In response to mechanical stimulation and calmodulin activation, Aqp8a.1 is incorporated into the plasma membrane, enabling cell volume loss that drives heart looping and valve formation.
βš–οΈ Piezo1 fine-tunes this process through a dual mechanism: in the short term, promoting membrane trafficking of Aqp8a.1 for rapid cell volume adjustment, and in the long term, suppressing aqp8a.1 transcription via Notch1b signaling to prevent excessive shrinkage.
πŸ’‘ Together, our findings reveal that mechanotransduction can dictate organ formation through the dynamic regulation of cell volume, uncovering a fundamental principle of morphogenesis.