Zebrafish Bashful/Laminin-alpha 1 Mutants Exhibit Multiple Axon Guidance Defects.
From: Department of Zoology, Cell and Molecular Biology Training Program, University of Wisconsin, Madison, Wisconsin, USA.
Developmental dynamics : an official publication of the American Association of Anatomists
- Publish Date: Jan 2006
- ISSN: 1058-8388
- Volume: 235
- Issue: 1
- Pages: 213-24
- Medium: Print
- Language: English
- Citation (JAMA): Paulus Jeremiah D, Halloran Mary C, et al. Zebrafish Bashful/Laminin-alpha 1 Mutants Exhibit Multiple Axon Guidance Defects.. Dev. Dyn. Jan 2006;235:213-24
Abstract
Laminin is known to provide a highly permissive substratum and in some cases directional information for axon outgrowth in vitro. However, there is still little known about laminin function in guiding axons in vivo. We investigated the axon guidance role of laminin-alpha1 in the developing zebrafish nervous system. Analysis of zebrafish bashful (bal)/laminin-a1 mutants revealed multiple functions for laminin-alpha1 in the outgrowth and guidance of central nervous system (CNS) axons. Most CNS axon pathways are defective in bal embryos. Some axon types, including retinal ganglion cell axons, early forebrain axons, and hindbrain reticulospinal axons, make specific pathfinding errors, suggesting laminin-alpha1 is required for directional decisions. Other axon tracts are defasciculated or not fully extended in bal embryos, suggesting a function for laminin-alpha1 in regulating adhesion or providing a permissive substratum for growth. In addition, some neurons have excessively branched axons in bal, indicating a potential role for laminin-alpha1 in branching. In contrast to CNS axons, most peripheral axons appear normal in bal mutants. Our results, thus, reveal important and diverse functions for laminin-alpha1 in guiding developing axons in vivo.
Mesh Headings (Keywords): Alleles, Animals, Axons, Cell Adhesion, Cell Movement, Cell Nucleus, Laminin, Mutation, Neurons, Rhombencephalon, Spinal Cord, Zebrafish
Check for Full Text / PubMed Unique Identifier (PMID): 16261616
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