Subrepellent doses of Slit1 promote Netrin-1 chemotactic responses in subsets of axons

Neural Dev. 2015 Mar 20:10:5. doi: 10.1186/s13064-015-0036-8.

Abstract

Background: Axon pathfinding is controlled by guidance cues that elicit specific attractive or repulsive responses in growth cones. It has now become clear that some cues such as Netrin-1 can trigger either attraction or repulsion in a context-dependent manner. In particular, it was recently found that the repellent Slit1 enables the attractive response of rostral thalamic axons to Netrin-1. This finding raised the intriguing possibility that Netrin-1 and Slit1, two essential guidance cues, may act more generally in an unexpected combinatorial manner to orient specific axonal populations. To address this major issue, we have used an innovative microfluidic device compatible not only with dissociated neuronal cultures but also with explant cultures to systematically and quantitatively characterize the combinatorial activity of Slit1 and Netrin-1 on rostral thalamic axons as well as on hippocampal neurons.

Results: We found that on rostral thalamic axons, only a subthreshold concentration of the repellent Slit1 triggered an attractive response to a gradient of Netrin-1. On hippocampal neurons, we similarly found that Slit1 alone is repulsive and a subthreshold concentration of Slit1 triggered a potent attractive or repulsive behavioral response to a gradient of Netrin-1, depending on the nature of the substrate.

Conclusions: Our study reveals that at subthreshold repulsive levels, Slit1 acts as a potent promoter of both Netrin-1 attractive and repulsive activities on distinct neuronal cell types, thereby opening novel perspectives on the role of combinations of cues in brain wiring.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axons / classification
  • Axons / drug effects*
  • Axons / physiology
  • Cell Culture Techniques / instrumentation
  • Cells, Cultured
  • Chemotaxis / drug effects*
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Hippocampus / cytology
  • Humans
  • Lab-On-A-Chip Devices*
  • Laminin / pharmacology
  • Mice
  • Microfluidic Analytical Techniques
  • Nerve Growth Factors / pharmacology*
  • Nerve Tissue Proteins / administration & dosage
  • Nerve Tissue Proteins / pharmacology*
  • Netrin-1
  • Organ Specificity
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / pharmacology
  • Thalamus / cytology
  • Tumor Suppressor Proteins / pharmacology*

Substances

  • Laminin
  • NTN1 protein, human
  • Nerve Growth Factors
  • Nerve Tissue Proteins
  • Ntn1 protein, mouse
  • Ntn1 protein, rat
  • Recombinant Proteins
  • SLIT1 protein, human
  • Slit1 protein, mouse
  • Tumor Suppressor Proteins
  • Netrin-1