Immunoreactivity of glucose transporter 8 is localized in the epithelial cells of the choroid plexus and in ependymal cells

Histochem Cell Biol. 2016 Aug;146(2):231-6. doi: 10.1007/s00418-016-1444-5. Epub 2016 May 9.

Abstract

High fructose intake is known to be associated with increased plasma triglyceride concentration, impaired glucose tolerance, insulin resistance, and high blood pressure. In addition, excess fructose intake is also thought to be a risk factor for dementia. Previous immunohistochemical studies have shown the presence of glucose transporter 5 (GLUT5), a major transporter of fructose, in the epithelial cells of the choroid plexus and ependymal cells in the brains of humans, rats, and mice, while GLUT2, a minor transporter of fructose, was localized in the ependymal cells of rat brain. In this study, immunoreactivity for the fructose transporter GLUT8 was observed in the cytoplasm of the epithelial cells in the choroid plexus and in the ependymal cells of the brains of humans and mice. These structures were not immunoreactive for GLUT7, GLUT11, and GLUT12. Our findings support the hypothesis of the transport of intravascular fructose through the epithelial cells of the choroid plexus and the ependymal cells.

Keywords: Choroid plexus; Ependymal cell; Fructose; GLUT8.

MeSH terms

  • Animals
  • Choroid Plexus / cytology*
  • Choroid Plexus / metabolism
  • Ependyma / cytology*
  • Ependyma / metabolism
  • Epithelial Cells / metabolism*
  • Glucose Transport Proteins, Facilitative / analysis*
  • Glucose Transport Proteins, Facilitative / metabolism*
  • Humans
  • Immunohistochemistry
  • Male
  • Mice
  • Mice, Inbred C3H

Substances

  • Glucose Transport Proteins, Facilitative
  • SLC2A8 protein, human
  • Slc2a8 protein, mouse