Netrin1 and reelin signaling are required for the migration of anterolateral system neurons in the embryonic spinal cord

Pain. 2022 Apr 1;163(4):e527-e539. doi: 10.1097/j.pain.0000000000002444.

Abstract

Projection neurons of the spinal cord dorsal horn which transmit pain, itch, and temperature information to the brain comprise the anterolateral system (AS). A recent molecular and genetic study showed that many developing AS neurons express the transcription factor Phox2a and provided insights into the mechanisms of their ontogeny and wiring of nociceptive neuronal circuits. Here, we show that the loss of the axonal guidance and neuronal migration signal netrin1 results in impaired migration of mouse Phox2a+ AS neurons into the spinal lamina I. Furthermore, we show that in the absence of Dab1, an intracellular transducer of the neuronal migration signal reelin, the migration of spinal lamina V and lateral spinal nucleus Phox2a+ AS neurons is impaired, in line with deficits in nociception seen in mice with a loss of reelin signaling. Together, these results provide evidence that netrin1 and reelin control the development of spinal nociceptive projection neurons, suggesting a mechanistic explanation for studies that link sequence variations in human genes encoding these neurodevelopmental signals and abnormal pain sensation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion Molecules, Neuronal* / genetics
  • Extracellular Matrix Proteins* / genetics
  • Homeodomain Proteins
  • Mice
  • Nerve Tissue Proteins / genetics
  • Neurons
  • Pain
  • Reelin Protein
  • Serine Endopeptidases / genetics
  • Spinal Cord
  • Spinal Cord Dorsal Horn

Substances

  • Cell Adhesion Molecules, Neuronal
  • Dab1 protein, mouse
  • Extracellular Matrix Proteins
  • Homeodomain Proteins
  • Nerve Tissue Proteins
  • Phox2a protein, mouse
  • Reelin Protein
  • Serine Endopeptidases