Netrin-1 and slit-2 regulate and direct neurite growth of ventral midbrain dopaminergic neurons

Mol Cell Neurosci. 2005 Mar;28(3):547-55. doi: 10.1016/j.mcn.2004.11.009.

Abstract

We investigated the roles of netrin-1 and slit-2 in regulation and navigation of dopamine (DA) axon growth using an explant culture preparation of embryonic ventral midbrain (embryonic day 14) and a co-culture system. We found that netrin-1 protein significantly enhanced DA axonal outgrowth and promoted DA axonal outgrowth in a co-culture system of netrin-1 expressing cells. Such effects were mediated by the receptor DCC as demonstrated by antibody perturbation of the DCC receptor. In contrast, slit-2 inhibited DA neuron extensions and repelled DA neurite growth. These slit-2 activities required robo receptors since the reduced neurite extension was abolished by addition of excess robo receptors. In this system, netrin-1 stimulated and slit-2 opposed DA neurite growth. Such regulation may be important for DA axonal maintenance, regeneration, and phenotypic target recognition.

Publication types

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

MeSH terms

  • Animals
  • Cell Adhesion Molecules / metabolism
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology*
  • Cell Line
  • Cells, Cultured
  • DCC Receptor
  • Dopamine / metabolism*
  • G Protein-Coupled Inwardly-Rectifying Potassium Channels
  • Growth Cones / metabolism
  • Growth Inhibitors / metabolism
  • Growth Substances / metabolism
  • Humans
  • Intercellular Signaling Peptides and Proteins
  • Mesencephalon / cytology
  • Mesencephalon / embryology*
  • Mesencephalon / metabolism
  • Nerve Growth Factors / metabolism*
  • Nerve Growth Factors / pharmacology
  • Nerve Tissue Proteins / metabolism*
  • Nerve Tissue Proteins / pharmacology
  • Netrin-1
  • Neurites / drug effects
  • Neurites / metabolism*
  • Neurites / ultrastructure
  • Potassium Channels, Inwardly Rectifying / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Cell Surface
  • Receptors, Immunologic / metabolism
  • Substantia Nigra / cytology
  • Substantia Nigra / embryology*
  • Substantia Nigra / metabolism
  • Tumor Suppressor Proteins / metabolism*
  • Tumor Suppressor Proteins / pharmacology
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Cell Adhesion Molecules
  • DCC Receptor
  • DCC protein, human
  • G Protein-Coupled Inwardly-Rectifying Potassium Channels
  • Growth Inhibitors
  • Growth Substances
  • Intercellular Signaling Peptides and Proteins
  • NTN1 protein, human
  • Nerve Growth Factors
  • Nerve Tissue Proteins
  • Ntn1 protein, rat
  • Potassium Channels, Inwardly Rectifying
  • ROBO2 protein, human
  • Receptors, Cell Surface
  • Receptors, Immunologic
  • Tumor Suppressor Proteins
  • Netrin-1
  • Tyrosine 3-Monooxygenase
  • Slit homolog 2 protein
  • Dopamine