Salamanders are able to regenerate full limbs following amputation and the regenerating limb grows until it catches up with the development of the intact contralateral limb. This is a remarkable example of growth control since the regenerated limb must grow to a size that is larger than it was at the time of amputation in order to accommodate to the animal’s growing body. Even more strikingly, when a salamander is given a complete amputation on one limb and a digit amputation on the other, regeneration of both structures is completed in approximately the same period. Thus, distally amputated limbs grow slower than proximally amputated ones, resulting in an overall length of regeneration that is independent of the tissue volume to be reformed. Although this phenomenon was first observed centuries ago, the underlying mechanisms are still unknown. Furthermore, whether such differences in growth are already encoded in undamaged tissues, or if the differences only arise during regeneration, is undetermined as well.
Differential adhesion strength and extracellular matrix (ECM) were reported along the proximodistal (PD) axis during axolotl limb regeneration. Therefore, considering that cell–cell interactions and cell-ECM interactions play key roles in force transmission to and between cells, controlling signalling pathways that regulate stem cell self-renewal and differentiation, we hypothesize that tissue mechanical properties are regulated in gradient along the PD axis and are thus majorly responsible for the differential growth rates observed during regeneration between proximally and distally-amputated limbs.
Therefore, the central aim of this project is understanding how biomechanical properties of tissues affect regeneration, which may have important implications for the design of biomaterials to be used in regenerative medicine.