Motor neurons use push-pull signals to direct vascular remodeling critical for their connectivity. Academic Article uri icon

Overview

abstract

  • The nervous system requires metabolites and oxygen supplied by the neurovascular network, but this necessitates close apposition of neurons and endothelial cells. We find motor neurons attract vessels with long-range VEGF signaling, but endothelial cells in the axonal pathway are an obstacle for establishing connections with muscles. It is unclear how this paradoxical interference from heterotypic neurovascular contacts is averted. Through a mouse mutagenesis screen, we show that Plexin-D1 receptor is required in endothelial cells for development of neuromuscular connectivity. Motor neurons release Sema3C to elicit short-range repulsion via Plexin-D1, thus displacing endothelial cells that obstruct axon growth. When this signaling pathway is disrupted, epaxial motor neurons are blocked from reaching their muscle targets and concomitantly vascular patterning in the spinal cord is altered. Thus, an integrative system of opposing push-pull cues ensures detrimental axon-endothelial encounters are avoided while enabling vascularization within the nervous system and along peripheral nerves.

publication date

  • October 13, 2022

Research

keywords

  • Semaphorins
  • Vascular Remodeling

Identity

PubMed Central ID

  • PMC10316999

Scopus Document Identifier

  • 85140992882

Digital Object Identifier (DOI)

  • 10.1016/j.neuron.2022.09.021

PubMed ID

  • 36240771

Additional Document Info

volume

  • 110

issue

  • 24