Voltage-gated sodium channel <i>scn8a</i> is required for innervation and regeneration of amputated adult zebrafish fins.

Abstract

Teleost fishes and urodele amphibians can regenerate amputated appendages, whereas this ability is restricted to digit tips in adult mammals. One key component of appendage regeneration is reinnervation of the wound area. However, how innervation is regulated in injured appendages of adult vertebrates has seen limited research attention. From a forward genetics screen for temperature-sensitive defects in zebrafish fin regeneration, we identified a mutation that disrupted regeneration while also inducing paralysis at the restrictive temperature. Genetic mapping and complementation tests identify a mutation in the major neuronal voltage-gated sodium channel (VGSC) gene <i>scn8ab</i>. Conditional disruption of <i>scn8ab</i> impairs early regenerative events, including blastema formation, but does not affect morphogenesis of established regenerates. Whereas <i>scn8ab</i> mutations reduced neural activity as expected, they also disrupted axon regrowth and patterning in fin regenerates, resulting in hypoinnervation. Our findings indicate that the activity of VGSCs plays a proregenerative role by promoting innervation of appendage stumps.