Establishment of neurovascular congruency in the mouse whisker system by an independent patterning mechanism

Neuron. 2013 Oct 16;80(2):458-69. doi: 10.1016/j.neuron.2013.09.005.

Abstract

Nerves and vessels often run parallel to one another, a phenomenon that reflects their functional interdependency. Previous studies have suggested that neurovascular congruency in planar tissues such as skin is established through a "one-patterns-the-other" model, in which either the nervous system or the vascular system precedes developmentally and then instructs the other system to form using its established architecture as a template. Here, we find that, in tissues with complex three-dimensional structures such as the mouse whisker system, neurovascular congruency does not follow the previous model but rather is established via a mechanism in which nerves and vessels are patterned independently. Given the diversity of neurovascular structures in different tissues, guidance signals emanating from a central organizer in the specific target tissue may act as an important mechanism to establish neurovascular congruency patterns that facilitate unique target tissue function.

Publication types

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

MeSH terms

  • Animals
  • Blood Vessels / growth & development
  • Blood Vessels / physiology*
  • Body Patterning / physiology*
  • Cells, Cultured
  • Cytoskeletal Proteins
  • Embryo, Mammalian
  • Gene Expression Regulation, Developmental / physiology
  • Glycoproteins / biosynthesis
  • Glycoproteins / physiology
  • Intracellular Signaling Peptides and Proteins
  • Membrane Glycoproteins / biosynthesis
  • Membrane Glycoproteins / physiology
  • Membrane Proteins / biosynthesis
  • Membrane Proteins / physiology
  • Mice
  • Mice, Transgenic
  • Nerve Tissue Proteins / biosynthesis
  • Nerve Tissue Proteins / physiology
  • Semaphorins
  • Sensory Receptor Cells / physiology*
  • Vibrissae / growth & development
  • Vibrissae / innervation*
  • Vibrissae / physiology*

Substances

  • Cytoskeletal Proteins
  • Glycoproteins
  • Intracellular Signaling Peptides and Proteins
  • Membrane Glycoproteins
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Plxnd1 protein, mouse
  • Sema3e protein, mouse
  • Semaphorins