Induction of presynaptic differentiation in cultured neurons by extracellular matrix components

Eur J Neurosci. 1999 Oct;11(10):3457-67. doi: 10.1046/j.1460-9568.1999.00766.x.

Abstract

Motoneurons reinnervating skeletal muscles form nerve terminals at sites of contact with a specialized basal lamina. To analyse the molecules and mechanisms that underly these responses, we introduce two systems in which basal lamina-derived components induce presynaptic differentiation of cultured neurons from chick ciliary ganglia in the absence of a postsynaptic cell. In one, ciliary neurites that contact substrates coated with a recombinant laminin beta2 fragment form varicosities that are rich in synaptic vesicle proteins, depleted of neurofilaments, and capable of depolarization-dependent exocytosis and endocytosis. Thus, a single molecule can trigger a complex, coordinated program of presynaptic differentiation. In a second system, neurites growing on cryostat sections of adult kidney form vesicle-rich, neurofilament-poor arbors on glomeruli. Glomerular basal lamina, like synaptic basal lamina, is rich in laminin beta2 and collagen (alpha3-5) IV. However, glomeruli from mutant mice lacking these proteins were capable of inducing differentiation, suggesting the glomerulus as a source of novel presynaptic organizing molecules.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Communication / drug effects
  • Cell Communication / physiology
  • Cell Culture Techniques / methods
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Chick Embryo
  • Ciliary Body / cytology
  • Extracellular Matrix Proteins / pharmacology*
  • Kidney Glomerulus / chemistry
  • Kidney Glomerulus / cytology
  • Laminin / pharmacology
  • Mice
  • Motor Neurons / cytology*
  • Motor Neurons / drug effects*
  • Muscle Fibers, Skeletal / cytology*
  • Muscle, Skeletal / cytology
  • Peptide Fragments / pharmacology
  • Presynaptic Terminals / physiology
  • Signal Transduction / drug effects
  • Signal Transduction / physiology

Substances

  • Extracellular Matrix Proteins
  • Laminin
  • Peptide Fragments