ADAM metalloproteases promote a developmental switch in responsiveness to the axonal repellant Sema3A

Nat Commun. 2014 Jun 5:5:4058. doi: 10.1038/ncomms5058.

Abstract

During embryonic development, axons can gain and lose sensitivity to guidance cues, and this flexibility is essential for the correct wiring of the nervous system. Yet, the underlying molecular mechanisms are largely unknown. Here we show that receptor cleavage by ADAM (A Disintegrin And Metalloprotease) metalloproteases promotes murine sensory axons loss of responsiveness to the chemorepellant Sema3A. Genetic ablation of ADAM10 and ADAM17 disrupts the developmental downregulation of Neuropilin-1 (Nrp1), the receptor for Sema3A, in sensory axons. Moreover, this is correlated with gain of repulsive response to Sema3A. Overexpression of Nrp1 in neurons reverses axonal desensitization to Sema3A, but this is hampered in a mutant Nrp1 with high susceptibility to cleavage. Lastly, we detect guidance errors of proprioceptive axons in ADAM knockouts that are consistent with enhanced response to Sema3A. Our results provide the first evidence for involvement of ADAMs in regulating developmental switch in responsiveness to axonal guidance cues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM Proteins / genetics*
  • ADAM10 Protein
  • ADAM17 Protein
  • Amyloid Precursor Protein Secretases / genetics
  • Animals
  • Axons / metabolism*
  • Gene Expression Regulation, Developmental*
  • Membrane Proteins / genetics
  • Mice
  • Neuropilin-1 / genetics*
  • Neuropilin-1 / metabolism
  • Rats
  • Semaphorin-3A / metabolism*
  • Sensory Receptor Cells / metabolism*

Substances

  • Membrane Proteins
  • Sema3a protein, mouse
  • Sema3a protein, rat
  • Semaphorin-3A
  • Neuropilin-1
  • Amyloid Precursor Protein Secretases
  • ADAM Proteins
  • ADAM10 Protein
  • ADAM10 protein, rat
  • Adam10 protein, mouse
  • ADAM17 Protein
  • Adam17 protein, mouse
  • Adam17 protein, rat