A novel pathogenesis of megacolon in Ncx/Hox11L.1 deficient mice

J Clin Invest. 1997 Aug 15;100(4):795-801. doi: 10.1172/JCI119593.

Abstract

The Ncx/Hox11L.1 gene, a member of the Hox11 homeobox gene family, is mainly expressed in neural crest-derived tissues. To elucidate the role of Ncx/Hox11L.1, the gene has been inactivated in embryonic stem cells by homologous recombination. The homozygous mutant mice were viable. These mice developed megacolon with enteric ganglia by age 3-5 wk. Histochemical analysis of the ganglia revealed that the enteric neurons hyperinnervated in the narrow segment of megacolon. Some of these neuronal cells degenerated and neuronal cell death occurred in later stages. We propose that Ncx/Hox11L.1 is required for maintenance of proper functions of the enteric nervous system. These mutant mice can be used to elucidate a novel pathogenesis for human neuronal intestinal dysplasia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Colon / chemistry
  • Colon / innervation*
  • Colon / pathology
  • Colon / ultrastructure
  • Enteric Nervous System / chemistry
  • Enteric Nervous System / ultrastructure
  • Ganglia / chemistry
  • Ganglia / pathology
  • Ganglia / ultrastructure
  • Homeodomain Proteins / metabolism
  • Homeodomain Proteins / physiology*
  • Immunohistochemistry
  • Megacolon / etiology*
  • Megacolon / genetics
  • Mice
  • Mice, Knockout
  • NADPH Dehydrogenase / analysis
  • Neuropeptide Y / analysis
  • Oncogene Proteins / deficiency
  • Oncogene Proteins / metabolism
  • Oncogene Proteins / physiology*
  • Substance P / analysis

Substances

  • Homeodomain Proteins
  • Neuropeptide Y
  • Oncogene Proteins
  • Tlx1 protein, mouse
  • Substance P
  • NADPH Dehydrogenase