Jonas Neipel @neipel.bsky.social · 20/07/2025(3/10) Jerome found cells moving to the left around the node, repositioning a Shh domain to the left, but what makes them do that? 110
Jonas Neipel @neipel.bsky.social · 20/07/2025(9/10) In conclusion, we give a mechanical perspective on how the node organises avian development: mechanical coupling of tissue layers allows for the generation of an active chiral torque dipole to break embryonic L/R symmetry. How is this achieved on a cell scale? Stay tuned! 110
Jonas Neipel @neipel.bsky.social · 20/07/2025(8/10) But now comes the really striking result: She found that replacing the meso-/endo tissue with a vitel. membrane is sufficient to restore node rotation. So, you simply need some mech. substrate. sustaining a counter-torque such that the node can drive its own rotation. 100
Jonas Neipel @neipel.bsky.social · 20/07/2025(7/10) But, what is the substrate? Is it the underlying meso-/endoderm? Here come the crazy experiments by Julia: She used an eye-brow to remove the meso-/endo showing that it’s required for node rotation. Notably, meso-/endo grows back yielding a delayed and reduced node rotation. 110
Jonas Neipel @neipel.bsky.social · 20/07/2025(6/10) So, the following picture following mechanical picture of avian L/R sym. break. emerges: actomyosin-activity generates cell-scale torque dipoles that propel the rotation of node and surrounding epiblast with respect to some rigid substrate. 100
Jonas Neipel @neipel.bsky.social · 20/07/2025(5/10) But is the node really capable of making itself rotate? Lasercuts by Julia show yes, providing maybe the first direct evidence for a tissue-scale active chiral torque. Also, we show that the apparent torque is actomyosin-dependent, consistent with previous observations by Jerome. 100
Jonas Neipel @neipel.bsky.social · 20/07/2025(4/10) We quantified these chiral tissue flows in 25 quail embryos and inferred forces using a fluid model, suggesting a torque of 6μNμm is generated locally at the node. 132