PUBLICATION

Myostatin is a negative regulator of adult neurogenesis after spinal cord injury in zebrafish

Authors
Saraswathy, V.M., Zhou, L., McAdow, A.R., Burris, B., Dogra, D., Reischauer, S., Mokalled, M.H.
ID
ZDB-PUB-221124-7
Date
2022
Source
Cell Reports   41: 111705111705 (Journal)
Registered Authors
Mokalled, Mayssa, Reischauer, Sven
Keywords
CP: Developmental biology, CP: Neuroscience, adult neurogenesis, eural stem cells, myostatin, neuronal differentiation, regeneration, spinal cord injury, zebrafish
Datasets
GEO:GSE183644
MeSH Terms
  • Adult
  • Animals
  • Fibroblast Growth Factor 1
  • Humans
  • Infant, Newborn
  • Mammals
  • Myostatin
  • Neurogenesis
  • Recovery of Function
  • Spinal Cord Injuries*/genetics
  • Zebrafish*
PubMed
36417881 Full text @ Cell Rep.
Abstract
Intrinsic and extrinsic inhibition of neuronal regeneration obstruct spinal cord (SC) repair in mammals. In contrast, adult zebrafish achieve functional recovery after complete SC transection. While studies of innate SC regeneration have focused on axon regrowth as a primary repair mechanism, how local adult neurogenesis affects functional recovery is unknown. Here, we uncover dynamic expression of zebrafish myostatin b (mstnb) in a niche of dorsal SC progenitors after injury. mstnb mutants show impaired functional recovery, normal glial and axonal bridging across the lesion, and an increase in the profiles of newborn neurons. Molecularly, neuron differentiation genes are upregulated, while the neural stem cell maintenance gene fgf1b is downregulated in mstnb mutants. Finally, we show that human fibroblast growth factor 1 (FGF1) treatment rescues the molecular and cellular phenotypes of mstnb mutants. These studies uncover unanticipated neurogenic functions for mstnb and establish the importance of local adult neurogenesis for innate SC repair.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping