Neural crest requires Impdh2 for development of the enteric nervous system, great vessels, and craniofacial skeleton

Dev Biol. 2016 Jan 1;409(1):152-165. doi: 10.1016/j.ydbio.2015.11.004. Epub 2015 Nov 10.

Abstract

Mutations that impair the proliferation of enteric neural crest-derived cells (ENCDC) cause Hirschsprung disease, a potentially lethal birth defect where the enteric nervous system (ENS) is absent from distal bowel. Inosine 5' monophosphate dehydrogenase (IMPDH) activity is essential for de novo GMP synthesis, and chemical inhibition of IMPDH induces Hirschsprung disease-like pathology in mouse models by reducing ENCDC proliferation. Two IMPDH isoforms are ubiquitously expressed in the embryo, but only IMPDH2 is required for life. To further understand the role of IMPDH2 in ENS and neural crest development, we characterized a conditional Impdh2 mutant mouse. Deletion of Impdh2 in the early neural crest using the Wnt1-Cre transgene produced defects in multiple neural crest derivatives including highly penetrant intestinal aganglionosis, agenesis of the craniofacial skeleton, and cardiac outflow tract and great vessel malformations. Analysis using a Rosa26 reporter mouse suggested that some or all of the remaining ENS in Impdh2 conditional-knockout animals was derived from cells that escaped Wnt1-Cre mediated DNA recombination. These data suggest that IMPDH2 mediated guanine nucleotide synthesis is essential for normal development of the ENS and other neural crest derivatives.

Keywords: De novo purine synthesis; Enteric nervous system; Neural crest.

Publication types

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

MeSH terms

  • Alleles
  • Animals
  • Bromodeoxyuridine / metabolism
  • Enteric Nervous System / blood supply*
  • Enteric Nervous System / embryology*
  • Enteric Nervous System / enzymology
  • Enteric Nervous System / pathology
  • Face / embryology*
  • Female
  • Fetus / abnormalities
  • Fetus / embryology
  • Gene Deletion
  • Genes, Reporter
  • Hirschsprung Disease / pathology
  • IMP Dehydrogenase / deficiency
  • IMP Dehydrogenase / metabolism*
  • In Situ Nick-End Labeling
  • Integrases / metabolism
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Myocardium / pathology
  • Neural Crest / embryology*
  • Neural Crest / enzymology*
  • Organ Specificity
  • RNA, Untranslated / metabolism
  • Recombination, Genetic / genetics
  • Skull / embryology*
  • Skull / metabolism
  • Wnt1 Protein / metabolism

Substances

  • Gt(ROSA)26Sor non-coding RNA, mouse
  • RNA, Untranslated
  • Wnt1 Protein
  • IMP Dehydrogenase
  • IMPDH2, mouse
  • Cre recombinase
  • Integrases
  • Bromodeoxyuridine