Initiation of olfactory placode development and neurogenesis is blocked in mice lacking both Six1 and Six4

Dev Biol. 2009 Feb 1;326(1):75-85. doi: 10.1016/j.ydbio.2008.10.039. Epub 2008 Nov 7.

Abstract

Mouse olfactory epithelium (OE) originates from ectodermally derived placode, the olfactory placode that arises at the anterior end of the neural plate. Tissue grafting and recombination experiments suggest that the placode is derived from a common preplacodal domain around the neural plate and its development is directed by signals arising from the underlying mesoderm and adjacent neuroectoderm. In mice, loss of Six1 affects OE morphogenesis but not placode formation. We show here that embryos lacking both Six1 and Six4 failed to form the olfactory placode but the preplacodal region appeared to be specified as judged by the expression of Eya2, which marks the common preplacodal domain, suggesting a synergistic requirement of Six1 and Six4 in patterning the preplacodal ectoderm to a morphologic placode. Our results show that Six1 and Six4 are coexpressed in the preplacodal ectoderm from E8.0. In the olfactory pit, Six4 expression was observed in the peripheral precursors that overlap with Mash1-expressing cells, the early committed neuronal lineage. In contrast, Six1 is highly distributed in the peripheral regions where stem cells reside at E10.5 and it overlaps with Sox2 expression. Both genes are expressed in the basal and apical neuronal progenitors in the OE. Analyses of Six1;Six4 double mutant embryos demonstrated that the slightly thickened epithelium observed in the mutant was not induced for neuronal development. In contrast, in Six1(-/-) embryos, all neuronal lineage markers were initially expressed but the pattern of their expression was altered. Although very few, the pioneer neurons were initially present in the Six1 mutant OE. However, neurogenesis ceased by E12.5 due to markedly increased cell apoptosis and reduced proliferation, thus defining the cellular defects occurring in Six1(-/-) OE that have not been previously observed. Our findings demonstrate that Six1/4 function at the top of early events controlling olfactory placode formation and neuronal development. Our analyses show that the threshold of Six1/4 may be crucial for the expression of olfactory specific genes and that Six1 and Six4 may act synergistically to mediate olfactory placode specification and patterning through Fgf and Bmp signaling pathways.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Body Patterning / physiology
  • Bone Morphogenetic Protein 4 / metabolism
  • Cell Lineage / physiology
  • Cell Proliferation
  • Ectoderm / cytology
  • Ectoderm / embryology
  • Fibroblast Growth Factors / metabolism
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / physiology*
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Mice
  • Mice, Mutant Strains
  • Mutation
  • Neurogenesis / physiology*
  • Neurons / cytology*
  • Neurons / physiology
  • Nuclear Proteins / metabolism
  • Olfactory Mucosa / cytology
  • Olfactory Mucosa / embryology*
  • Protein Tyrosine Phosphatases / metabolism
  • Trans-Activators / genetics
  • Trans-Activators / physiology*

Substances

  • Ascl1 protein, mouse
  • Basic Helix-Loop-Helix Transcription Factors
  • Bmp4 protein, mouse
  • Bone Morphogenetic Protein 4
  • Homeodomain Proteins
  • Intracellular Signaling Peptides and Proteins
  • Nuclear Proteins
  • Six1 protein, mouse
  • Six4 protein, mouse
  • Trans-Activators
  • Fibroblast Growth Factors
  • Eya2 protein, mouse
  • Protein Tyrosine Phosphatases