Genetic specification of left-right asymmetry in the diaphragm muscles and their motor innervation

Elife. 2017 Jun 22;6:e18481. doi: 10.7554/eLife.18481.

Abstract

The diaphragm muscle is essential for breathing in mammals. Its asymmetric elevation during contraction correlates with morphological features suggestive of inherent left-right (L/R) asymmetry. Whether this asymmetry is due to L versus R differences in the muscle or in the phrenic nerve activity is unknown. Here, we have combined the analysis of genetically modified mouse models with transcriptomic analysis to show that both the diaphragm muscle and phrenic nerves have asymmetries, which can be established independently of each other during early embryogenesis in pathway instructed by Nodal, a morphogen that also conveys asymmetry in other organs. We further found that phrenic motoneurons receive an early L/R genetic imprint, with L versus R differences both in Slit/Robo signaling and MMP2 activity and in the contribution of both pathways to establish phrenic nerve asymmetry. Our study therefore demonstrates L-R imprinting of spinal motoneurons and describes how L/R modulation of axon guidance signaling helps to match neural circuit formation to organ asymmetry.

Keywords: Nodal; Slit/Robo; axon guidance; developmental biology; diaphragm; left/right asymmetry; motoneuron; mouse; neuroscience; stem cells.

Publication types

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

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Diaphragm / embryology*
  • Diaphragm / innervation*
  • Gene Expression Profiling
  • Mice
  • Motor Neurons / physiology
  • Neural Pathways / embryology*
  • Nodal Protein / metabolism
  • Phrenic Nerve / embryology*
  • Signal Transduction

Substances

  • Nodal Protein
  • Nodal protein, mouse