Skip to Content
Merck
  • Neural stem/progenitor cells are activated during tail regeneration in the leopard gecko (Eublepharis macularius).

Neural stem/progenitor cells are activated during tail regeneration in the leopard gecko (Eublepharis macularius).

The Journal of comparative neurology (2017-10-06)
E A B Gilbert, M K Vickaryous
ABSTRACT

As for many lizards, the leopard gecko (Eublepharis macularius) can self-detach its tail to avoid predation and then regenerate a replacement. The replacement tail includes a regenerated spinal cord with a simple morphology: an ependymal layer surrounded by nerve tracts. We hypothesized that cells within the ependymal layer of the original spinal cord include populations of neural stem/progenitor cells (NSPCs) that contribute to the regenerated spinal cord. Prior to tail loss, we performed a bromodeoxyuridine pulse-chase experiment and found that a subset of ependymal layer cells (ELCs) were label-retaining after a 140-day chase period. Next, we conducted a detailed spatiotemporal characterization of these cells before, during, and after tail regeneration. Our findings show that SOX2, a hallmark protein of NSPCs, is constitutively expressed by virtually all ELCs before, during, and after regeneration. We also found that during regeneration, ELCs express an expanded panel of NSPC and lineage-restricted progenitor cell markers, including MSI-1, SOX9, and TUJ1. Using electron microscopy, we determined that multiciliated, uniciliated, and biciliated cells are present, although the latter was only observed in regenerated spinal cords. Our results demonstrate that cells within the ependymal layer of the original, regenerating and fully regenerate spinal cord represent a heterogeneous population. These include radial glia comparable to Type E and Type B cells, and a neuronal-like population of cerebrospinal fluid-contacting cells. We propose that spinal cord regeneration in geckos represents a truncation of the restorative trajectory observed in some urodeles and teleosts, resulting in the formation of a structurally distinct replacement.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Anti-Musashi-1 Antibody, clone 7B11.1, clone 7B11.1, from mouse
Sigma-Aldrich
Anti-BrdU antibody, Mouse monoclonal, clone BU-33, purified from hybridoma cell culture
Sigma-Aldrich
Anti-Musashi-1 Antibody, Chemicon®, from rabbit
Sigma-Aldrich
Anti-NeuN Antibody (rabbit), from rabbit, purified by affinity chromatography
Sigma-Aldrich
Anti-Tubulin β III Antibody, Chemicon®, from mouse