Progenitor-derived glia are required for spinal cord regeneration in zebrafish

Author:

Zhou Lili12,McAdow Anthony R.12,Yamada Hunter12,Burris Brooke12ORCID,Klatt Shaw Dana12,Oonk Kelsey3,Poss Kenneth D.3,Mokalled Mayssa H.12ORCID

Affiliation:

1. Washington University School of Medicine 1 Department of Developmental Biology , , St. Louis, MO 63110, USA

2. Center of Regenerative Medicine, Washington University School of Medicine 2 , St. Louis, MO 63110, USA

3. Duke Regeneration Center, Department of Cell Biology, Duke University Medical Center 3 , Durham, NC 27710 , USA

Abstract

ABSTRACT Unlike mammals, adult zebrafish undergo spontaneous recovery after major spinal cord injury. Whereas reactive gliosis presents a roadblock for mammalian spinal cord repair, glial cells in zebrafish elicit pro-regenerative bridging functions after injury. Here, we perform genetic lineage tracing, assessment of regulatory sequences and inducible cell ablation to define mechanisms that direct the molecular and cellular responses of glial cells after spinal cord injury in adult zebrafish. Using a newly generated CreERT2 transgenic line, we show that the cells directing expression of the bridging glial marker ctgfa give rise to regenerating glia after injury, with negligible contribution to either neuronal or oligodendrocyte lineages. A 1 kb sequence upstream of the ctgfa gene was sufficient to direct expression in early bridging glia after injury. Finally, ablation of ctgfa-expressing cells using a transgenic nitroreductase strategy impaired glial bridging and recovery of swim behavior after injury. This study identifies key regulatory features, cellular progeny, and requirements of glial cells during innate spinal cord regeneration.

Funder

National Institutes of Health

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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