Opposing FGF and retinoid pathways control ventral neural pattern, neuronal differentiation, and segmentation during body axis extension

Neuron. 2003 Sep 25;40(1):65-79. doi: 10.1016/s0896-6273(03)00565-8.

Abstract

Vertebrate body axis extension involves progressive generation and subsequent differentiation of new cells derived from a caudal stem zone; however, molecular mechanisms that preserve caudal progenitors and coordinate differentiation are poorly understood. FGF maintains caudal progenitors and its attenuation is required for neuronal and mesodermal differentiation and to position segment boundaries. Furthermore, somitic mesoderm promotes neuronal differentiation in part by downregulating Fgf8. Here we identify retinoic acid (RA) as this somitic signal and show that retinoid and FGF pathways have opposing actions. FGF is a general repressor of differentiation, including ventral neural patterning, while RA attenuates Fgf8 in neuroepithelium and paraxial mesoderm, where it controls somite boundary position. RA is further required for neuronal differentiation and expression of key ventral neural patterning genes. Our data demonstrate that FGF and RA pathways are mutually inhibitory and suggest that their opposing actions provide a global mechanism that controls differentiation during axis extension.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / physiology*
  • Chick Embryo
  • Cleavage Stage, Ovum / cytology
  • Cleavage Stage, Ovum / metabolism
  • Fibroblast Growth Factor 8
  • Fibroblast Growth Factors / genetics
  • Fibroblast Growth Factors / metabolism*
  • Gene Expression Regulation, Developmental / physiology
  • Humans
  • Mice
  • Neural Inhibition / physiology
  • Neural Pathways / embryology
  • Neural Pathways / metabolism
  • Neurons / cytology
  • Neurons / metabolism*
  • Somites / cytology
  • Somites / metabolism
  • Spinal Cord / cytology
  • Spinal Cord / embryology
  • Spinal Cord / metabolism*
  • Tretinoin / metabolism*

Substances

  • FGF8 protein, human
  • Fgf8 protein, mouse
  • Fibroblast Growth Factor 8
  • Tretinoin
  • Fibroblast Growth Factors