Buckling instability underlies vertebral segmentation during axolotl tail regeneration
Masselink, W.; Gerber, T.; Singh Jamwal, V.; Falcon, F.; Deshayes, T.; Grindle, R.; Seaman, R. P.; Röcklinger, M.; Papadopoulos, S.-C.; Deneke, G.; Adhikary, A.; Andriotis, O. G.; Pende, M.; Taniguchi-Sugiura, Y.; Lin, T.-Y.; Kurth, T.; Wang, J.; Arendt, D.; Fei, J.-F.; Treutlein, B.; Kolling, F. W.; Thurner, P. J.; Graber, J. H.; Hannezo, E.; Tanaka, E. M.; Murawala, P.
Show abstract
Primary body-axis development is a highly conserved process that proceeds through somitogenesis and subsequent subdivision into dermatome, myotome, and sclerotome. Defects in somitic-clock genes such as Hes7 lead to vertebral-segmentation defects in mice and fish. Here we show that in the axolotl, although Hes7 is necessary for proper embryonic vertebral segmentation, it is-- surprisingly--dispensable during tail regeneration. We investigated the mechanism of vertebral segmentation during regeneration which initially occurs through extension of a cartilage rod ventral to the spinal cord. We find that the regenerating cartilage rod undergoes a periodic wrinkling that provides a template for vertebral segmentation. Via direct mechanical measurements and biophysical perturbations, we show that a model of compression-induced buckling instability can predict vertebral segmentation. The cartilage rod and other somitic derivatives (muscle, cartilage, tendon, fibroblasts) arise from tendon-like, Lfng+ multi-potent mesenchymal progenitors, which display a gene regulatory state distinct from somitic progenitors. In summary, we uncover a mechanism of vertebral segmentation during axolotl tail regeneration that is distinct from the somite-based developmental mechanism.
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