PUBLICATION
Characterizing the diverse cells that associate with the developing commissures of the zebrafish forebrain
- Authors
- Schnabl, J., Litz, M.P.H., Schneider, C., PenkoffLidbeck, N., Bashiruddin, S., Schwartz, M.S., Alligood, K., Devoto, S.H., Barresi, M.J.F.
- ID
- ZDB-PUB-201215-11
- Date
- 2020
- Source
- Developmental Neurobiology 81(5): 671-695 (Journal)
- Registered Authors
- Barresi, Michael J. F., Devoto, Stephen Henri, PenkoffLidbeck, Nadia, Schnabl, Jake
- Keywords
- Gfap, commissure, forebrain, glia, zebrafish
- MeSH Terms
-
- Animals
- Axons/metabolism
- Neurons/metabolism
- Prosencephalon*
- Zebrafish*/metabolism
- Zebrafish Proteins/metabolism
- PubMed
- 33314626 Full text @ Dev. Neurobiol.
Citation
Schnabl, J., Litz, M.P.H., Schneider, C., PenkoffLidbeck, N., Bashiruddin, S., Schwartz, M.S., Alligood, K., Devoto, S.H., Barresi, M.J.F. (2020) Characterizing the diverse cells that associate with the developing commissures of the zebrafish forebrain. Developmental Neurobiology. 81(5):671-695.
Abstract
During embryonic development of bilaterally symmetrical organisms, neurons send axons across the midline at specific points to connect the two halves of the nervous system with a commissure. Little is known about the cells at the midline that facilitate this tightly regulated process. We exploit the conserved process of vertebrate embryonic development in the zebrafish model system to elucidate the identity of cells at the midline that may facilitate postoptic (POC) and anterior commissure (AC) development. We have discovered that three different gfap+ astroglial cell morphologies persist in contact with pathfinding axons throughout commissure formation. Similarly, olig2+ progenitor cells occupy delineated portions of the postoptic and anterior commissures where they act as multipotent, neural progenitors. Moreover, we conclude that both gfap+ and olig2+ progenitor cells give rise to neuronal populations in both the telencephalon and diencephalon; however, these varied cell populations showed significant developmental timing differences between the telencephalon and diencephalon. Lastly, we also showed that fli1a+ mesenchymal cells migrate along the presumptive commissure regions before and during midline axon crossing. Furthermore, following commissure maturation, specific blood vessels formed at the midline of the POC and immediately ventral and parallel to the AC. This comprehensive account of the cellular populations that correlate with the timing and position of commissural axon pathfinding has supported the conceptual modeling and identification of the early forebrain architecture that may be necessary for proper commissure development.
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Human Disease / Model
Sequence Targeting Reagents
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