Enteric Glia Regulate Gastrointestinal Motility but Are Not Required for Maintenance of the Epithelium in Mice

Gastroenterology. 2017 Oct;153(4):1068-1081.e7. doi: 10.1053/j.gastro.2017.07.002. Epub 2017 Jul 13.

Abstract

Background & aims: When the glial fibrillary acidic protein (GFAP) promoter is used to express cellular toxins that eliminate glia in mice, intestinal epithelial permeability and proliferation increase; this led to the concept that glia are required for maintenance of the gastrointestinal epithelium. Many enteric glia, however, particularly in the mucosa, do not express GFAP. In contrast, virtually all enteric glia express proteolipid protein 1 (PLP1). We investigated whether elimination of PLP1-expressing cells compromises epithelial maintenance or gastrointestinal motility.

Methods: We generated mice that express tamoxifen-inducible Cre recombinase under control of the Plp1 promoter and carry the diptheria toxin subunit A (DTA) transgene in the Rosa26 locus (Plp1CreER;Rosa26DTA mice). In these mice, PLP1-expressing glia are selectively eliminated without affecting neighboring cells. We measured epithelial barrier function and gastrointestinal motility in these mice and littermate controls, and analyzed epithelial cell proliferation and ultrastructure from their intestinal tissues. To compare our findings with those from previous studies, we also eliminated glia with ganciclovir in GfapHSV-TK mice.

Results: Expression of DTA in PLP1-expressing cells selectively eliminated enteric glia from the small and large intestines, but caused no defects in epithelial proliferation, barrier integrity, or ultrastructure. In contrast, administration of ganciclovir to GfapHSV-TK mice eliminated fewer glia but caused considerable non-glial toxicity and epithelial cell death. Elimination of PLP1-expressing cells did not reduce survival of neurons in the intestine, but altered gastrointestinal motility in female, but not male, mice.

Conclusions: Using the Plp1 promoter to selectively eliminate glia in mice, we found that enteric glia are not required for maintenance of the intestinal epithelium, but are required for regulation of intestinal motility in females. Previous observations supporting the concept that maintenance of the intestinal epithelium requires enteric glia can be attributed to non-glial toxicity in GfapHSV-TK mice and epithelial-cell expression of GFAP. Contrary to widespread notions, enteric glia are therefore not required for epithelial homeostasis. However, they regulate intestinal motility in a sex-dependent manner.

Keywords: Enteric Nervous System; Epithelial Barrier; Sex Differences.

MeSH terms

  • Animals
  • Cell Proliferation
  • Diphtheria Toxin / genetics
  • Diphtheria Toxin / metabolism
  • Enteric Nervous System / metabolism
  • Enteric Nervous System / physiology*
  • Enteric Nervous System / ultrastructure
  • Female
  • Ganciclovir / toxicity
  • Gastrointestinal Motility*
  • Genotype
  • Glial Fibrillary Acidic Protein / genetics
  • Glial Fibrillary Acidic Protein / metabolism
  • Homeostasis
  • Integrases / genetics
  • Integrases / metabolism
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / physiology*
  • Intestinal Mucosa / ultrastructure
  • Intestines / drug effects
  • Intestines / innervation*
  • Intestines / ultrastructure
  • Male
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Myelin Proteolipid Protein / genetics
  • Neuroglia / metabolism
  • Neuroglia / physiology*
  • Neuroglia / ultrastructure
  • Peptide Fragments / genetics
  • Peptide Fragments / metabolism
  • Phenotype
  • Promoter Regions, Genetic
  • RNA, Untranslated / genetics
  • Sex Factors
  • Time Factors

Substances

  • Diphtheria Toxin
  • Glial Fibrillary Acidic Protein
  • Gt(ROSA)26Sor non-coding RNA, mouse
  • Myelin Proteolipid Protein
  • Peptide Fragments
  • Plp1 protein, mouse
  • RNA, Untranslated
  • diphtheria toxin fragment A
  • glial fibrillary astrocytic protein, mouse
  • Cre recombinase
  • Integrases
  • Ganciclovir