The Hlx homeobox transcription factor is required early in enteric nervous system development

BMC Dev Biol. 2006 Jul 19:6:33. doi: 10.1186/1471-213X-6-33.

Abstract

Background: Development of the enteric nervous system (ENS) requires interactions between migrating neural crest cells and the nascent gastrointestinal tract that are dependent upon genes expressed by both cell compartments. Hlx, a homeobox transcription factor gene that is expressed in mouse intestinal and hepatic mesenchyme, is required for normal embryonic growth of intestine and liver, and the Hlx-/- genotype is embryonic lethal. We hypothesized that Hlx is required for ENS development.

Results: Enteric neurons were identified in Hlx+/+ and Hlx-/- mouse embryos by immunostaining of embryo sections for the neural markers PGP9.5 and Phox2b, or by staining for beta-galactosidase in whole-mount embryos containing the dopamine beta-hydroxylase-nLacZ transgene. In Hlx+/+ embryos, neural crest cells/enteric neurons have moved from the stomach into the intestine by E10.5. By contrast, neural crest cells/enteric neurons remain largely restricted to the lateral stomach mesenchyme of Hlx-/- embryos, with only a few scattered neural crest cells/enteric neurons in the intestine between E10.5-16.5.

Conclusion: The Hlx homeobox transcription factor is required for early aspects of ENS development.

Publication types

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

MeSH terms

  • Animals
  • Dopamine beta-Hydroxylase / genetics
  • Dopamine beta-Hydroxylase / metabolism
  • Enteric Nervous System / embryology*
  • Enteric Nervous System / metabolism
  • Female
  • Gastrointestinal Tract / embryology
  • Gastrointestinal Tract / metabolism
  • Gene Expression Regulation, Developmental / genetics
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism*
  • Immunohistochemistry / methods
  • Lac Operon / genetics
  • Male
  • Mesoderm / cytology
  • Mesoderm / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Neurons / cytology
  • Neurons / metabolism
  • Time Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • beta-Galactosidase / metabolism

Substances

  • Hlx protein, mouse
  • Homeodomain Proteins
  • Transcription Factors
  • Dopamine beta-Hydroxylase
  • beta-Galactosidase