The involvement of axonin-1/SC2 in mediating notochord-derived chemorepulsive activities for dorsal root ganglion neurites

Dev Biol. 2000 Aug 15;224(2):112-21. doi: 10.1006/dbio.2000.9813.

Abstract

Previous studies have suggested that the developing notochord secretes diffusible axon guidance molecules that repel dorsal root ganglion (DRG) neurites (R. Keynes et al., 1997, Neuron 18, 889-897; K. Nakamoto and T. Shiga, 1998, Dev. Biol. 202, 304-314). Neither notochord-derived chemorepellents nor their receptors on DRG neurites are, however, known. Here we investigated whether cell adhesion molecules (CAMs) of the immunoglobulin/fibronectin type III subfamily present on DRG neurites, including axonin-1/SC2, N-CAM, Ng-CAM, and Nr-CAM, are required for mediating the notochord-derived chemorepulsion. Using collagen gel cocultures of DRGs and notochord explants, we found that an antibody against axonin-1/SC2 diminished the effects of the chemorepulsive activity from the notochord, whereas antibodies against N-CAM, Ng-CAM, and Nr-CAM had no effect. We further showed that the removal of glycosylphosphatidylinositol-anchored cell surface molecules, including axonin-1/SC2, from DRG neurites diminished the effects of the notochord-derived chemorepulsive activity to an extent similar to that of treatment with the anti-axonin-1/SC2 antibody. These results suggest that axonin-1/SC2 expressed on DRG neurites may be involved in mediating the notochord-derived chemorepulsive activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion Molecules, Neuronal / physiology*
  • Chemotaxis / drug effects
  • Chemotaxis / physiology*
  • Chick Embryo
  • Contactin 2
  • Ganglia, Spinal / physiology*
  • Immunohistochemistry
  • Neurites / physiology*
  • Notochord / physiology*
  • Phosphatidylinositol Diacylglycerol-Lyase
  • Type C Phospholipases / pharmacology

Substances

  • Cell Adhesion Molecules, Neuronal
  • Contactin 2
  • Type C Phospholipases
  • Phosphatidylinositol Diacylglycerol-Lyase