PUBLICATION

Semaphorin3D regulates axon axon interactions by modulating levels of L1 cell adhesion molecule

Authors
Wolman, M.A., Regnery, A.M., Becker, T., Becker, C.G., and Halloran, M.C.
ID
ZDB-PUB-080513-1
Date
2007
Source
The Journal of neuroscience : the official journal of the Society for Neuroscience   27(36): 9653-9663 (Journal)
Registered Authors
Becker, Catherina G., Becker, Thomas, Halloran, Mary, Wolman, Marc
Keywords
semaphorin, L1, axon guidance, fasciculation, adhesion, zebrafish
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Axons/metabolism
  • Axons/physiology*
  • Embryo, Nonmammalian
  • Gene Expression/drug effects
  • Green Fluorescent Proteins/genetics
  • Growth Cones/drug effects
  • Growth Cones/metabolism
  • Nerve Growth Factors/genetics
  • Nerve Growth Factors/physiology*
  • Neural Cell Adhesion Molecule L1/genetics
  • Neural Cell Adhesion Molecule L1/metabolism*
  • Neuropilin-1/genetics
  • Neuropilin-1/metabolism
  • Oligonucleotides, Antisense/pharmacology
  • Rhombencephalon/embryology
  • Rhombencephalon/metabolism
  • Semaphorins/genetics
  • Semaphorins/physiology*
  • Zebrafish
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/physiology*
PubMed
17804626 Full text @ J. Neurosci.
Abstract
The decision of a growing axon to selectively fasciculate with and defasciculate from other axons is critical for axon pathfinding and target innervation. Fasciculation can be regulated by cell adhesion molecules that modulate interaxonal adhesion and repulsive molecules, expressed by surrounding tissues that channel axons together. Here we describe crosstalk between molecules that mediate these mechanisms. We show that Semaphorin3D (Sema3D), a classic repulsive molecule, promotes fasciculation by regulating L1 CAM levels and axon-axon interactions rather than by creating a repulsive surround. Knockdown experiments show that Sema3D and L1 genetically interact to promote fasciculation. Sema3D overexpression increases and Sema3D knockdown decreases levels of axonal L1 protein. Moreover, excess L1 rescues defasciculation caused by the loss of Sema3D. In vivo time-lapse imaging reveals that Sema3D or L1 knockdown cause identical defects in growth cone behaviors during axon-axon interactions, consistent with a loss of adhesion. These results reveal a novel mechanism by which a semaphorin promotes fasciculation and modulates axon-axon interactions by regulating an adhesion molecule.
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Errata and Notes