Immunohistochemical characterization of cell types expressing the cellular prion protein in the small intestine of cattle and mice

Histochem Cell Biol. 2007 Mar;127(3):291-301. doi: 10.1007/s00418-006-0250-x. Epub 2006 Dec 13.

Abstract

The gastrointestinal tract is thought to be the main site of entry for the pathological isoform of the prion protein (PrP(Sc)). Prion diseases are believed to result from a conformational change of the cellular prion protein (PrP(c)) to PrP(Sc). Therefore, PrP(c) expression is a prerequisite for the infection and spread of the disease to the central nervous system. However, the distribution of PrP(c) in the gut is still a matter of controversy. We therefore investigated the localization of PrP(c) in the bovine and murine small intestine. In cattle, most PrP(c) positive epithelial cells were detected in the duodenum, while a few positive cells were found in the jejunum. PrP(c) was expressed in serotonin producing cells. In bovine Peyer's patches, PrP(c) was distributed in extrafollicular areas, but not in the germinal centre of the jejunum and ileum. PrP(c) was expressed in myeloid lineage cells such as myeloid dendritic cells and macrophages. In mice, PrP(c) was expressed in some epithelial cells throughout the small intestine as well as in cells such as follicular dendritic cell in the germinal centre of Peyer's patches. In this study, we demonstrate that there are a number of differences in the localization of PrP(c) between the murine and bovine small intestines.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Dendritic Cells / metabolism
  • Dendritic Cells / pathology
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • Immunohistochemistry / methods*
  • Intestine, Small / metabolism*
  • Intestine, Small / pathology*
  • Macrophages / metabolism
  • Macrophages / pathology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Peyer's Patches / metabolism
  • Peyer's Patches / pathology
  • PrPC Proteins / genetics*
  • PrPC Proteins / metabolism
  • Prions / administration & dosage
  • Prions / genetics
  • Prions / metabolism*

Substances

  • PrPC Proteins
  • Prions