PUBLICATION

Injury-induced ctgfa directs glial bridging and spinal cord regeneration in zebrafish

Authors
Mokalled, M.H., Patra, C., Dickson, A.L., Endo, T., Stainier, D.Y., Poss, K.D.
ID
ZDB-PUB-161105-13
Date
2016
Source
Science (New York, N.Y.)   354: 630-634 (Journal)
Registered Authors
Dickson, Amy, Mokalled, Mayssa, Poss, Kenneth D., Stainier, Didier
Keywords
none
Datasets
GEO:GSE77025
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Connective Tissue Growth Factor/genetics
  • Connective Tissue Growth Factor/physiology*
  • Female
  • Male
  • Mutation
  • Neuroglia/physiology*
  • Spinal Cord Injuries/physiopathology*
  • Spinal Cord Regeneration*/genetics
  • Zebrafish/genetics
  • Zebrafish/physiology*
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/physiology*
PubMed
27811277 Full text @ Science
Abstract
Unlike mammals, zebrafish efficiently regenerate functional nervous system tissue after major spinal cord injury. Whereas glial scarring presents a roadblock for mammalian spinal cord repair, glial cells in zebrafish form a bridge across severed spinal cord tissue and facilitate regeneration. We performed a genome-wide profiling screen for secreted factors that are up-regulated during zebrafish spinal cord regeneration. We found that connective tissue growth factor a (ctgfa) is induced in and around glial cells that participate in initial bridging events. Mutations in ctgfa disrupted spinal cord repair, and transgenic ctgfa overexpression or local delivery of human CTGF recombinant protein accelerated bridging and functional regeneration. Our study reveals that CTGF is necessary and sufficient to stimulate glial bridging and natural spinal cord regeneration.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutation and Transgenics
Human Disease / Model Data
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping
Errata and Notes