Neural crest contribution to lingual mesenchyme, epithelium and developing taste papillae and taste buds

Dev Biol. 2012 Aug 15;368(2):294-303. doi: 10.1016/j.ydbio.2012.05.028. Epub 2012 May 31.

Abstract

The epithelium of mammalian tongue hosts most of the taste buds that transduce gustatory stimuli into neural signals. In the field of taste biology, taste bud cells have been described as arising from "local epithelium", in distinction from many other receptor organs that are derived from neurogenic ectoderm including neural crest (NC). In fact, contribution of NC to both epithelium and mesenchyme in the developing tongue is not fully understood. In the present study we used two independent, well-characterized mouse lines, Wnt1-Cre and P0-Cre that express Cre recombinase in a NC-specific manner, in combination with two Cre reporter mouse lines, R26R and ZEG, and demonstrate a contribution of NC-derived cells to both tongue mesenchyme and epithelium including taste papillae and taste buds. In tongue mesenchyme, distribution of NC-derived cells is in close association with taste papillae. In tongue epithelium, labeled cells are observed in an initial scattered distribution and progress to a clustered pattern between papillae, and within papillae and early taste buds. This provides evidence for a contribution of NC to lingual epithelium. Together with previous reports for the origin of taste bud cells from local epithelium in postnatal mouse, we propose that NC cells migrate into and reside in the epithelium of the tongue primordium at an early embryonic stage, acquire epithelial cell phenotypes, and undergo cell proliferation and differentiation that is involved in the development of taste papillae and taste buds. Our findings lead to a new concept about derivation of taste bud cells that include a NC origin.

Publication types

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

MeSH terms

  • Animals
  • Animals, Newborn
  • Epithelium / embryology
  • Epithelium / growth & development
  • Epithelium / metabolism
  • Female
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Immunohistochemistry
  • Integrases / genetics
  • Integrases / metabolism
  • Male
  • Mesoderm / embryology
  • Mesoderm / growth & development
  • Mesoderm / metabolism*
  • Mice
  • Mice, Transgenic
  • Microscopy, Confocal
  • Models, Anatomic
  • Neural Crest / embryology
  • Neural Crest / growth & development
  • Neural Crest / metabolism*
  • Taste Buds / embryology
  • Taste Buds / growth & development
  • Taste Buds / metabolism*
  • Time Factors
  • Tongue / embryology
  • Tongue / growth & development
  • Tongue / metabolism*
  • Wnt1 Protein / genetics
  • Wnt1 Protein / metabolism
  • beta-Galactosidase / genetics
  • beta-Galactosidase / metabolism

Substances

  • Wnt1 Protein
  • Wnt1 protein, mouse
  • Green Fluorescent Proteins
  • Cre recombinase
  • Integrases
  • beta-Galactosidase