Premium
Cells lining the lateral ventricle show dynamic protein expression following tail loss in the leopard gecko
Author(s) -
McDonald Rebecca Paula,
Gilbert Emily Anne Beatrice,
Macdonald Alaina,
Vickaryous Matthew Kenneth
Publication year - 2016
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.30.1_supplement.562.6
Subject(s) - biology , sox2 , progenitor cell , dentate gyrus , population , microbiology and biotechnology , neurogenesis , neural stem cell , central nervous system , stem cell , neuroscience , pathology , anatomy , medicine , transcription factor , biochemistry , environmental health , gene
Neural stem progenitor cells (NSPCs) have been identified in the adult mammalian central nervous system, specifically in the dentate gyrus of the hippocampus and in the subventricular zone of the lateral ventricle. Despite this, mammals are incapable of central nervous system regeneration following injury. In contrast, many lizard species can regenerate their spinal cord (following tail loss) and some can even repair the optic nerve and parts of the brain. However, the source of cells contributing to brain regeneration remains unclear. Here we characterize cells lining the lateral ventricle of the brain in the leopard gecko, Eublepharis macularius. We show that these ventricular lining, or periventricular cells are a potential progenitor population capable of responding to central nervous system injury. Using a bromodeoxyuridine (BrdU) pulse‐chase experiment we determined that, prior to injury, periventricular cells are slow‐cycling. Moreover, periventricular cells show widespread expression of several common NSPC markers, including the transcription factor Sox2 and the intermediate filament glial fibrillary acidic protein (GFAP). In addition, a subset of periventricular cells express the neural progenitor cell marker Sox9. Following injury to the spinal cord (as a result of tail loss) populations of periventricular cells lining the lateral ventricle continue to express NSPC markers but also begin to proliferate, as evidenced by expression of both proliferating cell nuclear antigen (PCNA) and phosphohistone H3. Intriguingly, some of these cells newly express HuC/D, a marker of neuronal differentiation. Dynamic protein expression by periventricular cells indicates that this population is activated in response to injury, and points towards their potential to participate in neural regeneration. Support or Funding Information Natural Sciences and Engineering Research Council (NSERC) Discovery Grant 400358