Functions of GI-GPx: lessons from selenium-dependent expression and intracellular localization

Biofactors. 2001;14(1-4):101-6. doi: 10.1002/biof.5520140114.

Abstract

Gastro intestinal glutathione peroxidase (GI-GPx) is one of the four distinct mammalian selenoperoxidases. It had been reported to be restricted to the gastrointestinal tract but has more recently been identified also in human liver and some tumor cell lines. GI-GPx ranks high in the hierarchy of selenoproteins. The GI-GPx mRNA rather increases than decreases in selenium deficiency. GI-GPx protein responds poorly to selenium deprivation and increases fast upon resupplementation. Putative biological roles of GI-GPx, e.g. protection against food-born hydroperoxides, redox-regulation of proliferation or apoptosis, and modulation of mucosal immunity, are discussed in the light of cellular and subcellular distribution, transcriptional regulation and observations with k.o. mice.

Publication types

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

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Transformation, Neoplastic
  • Glutathione Peroxidase / genetics*
  • Glutathione Peroxidase / metabolism*
  • Humans
  • Intestinal Mucosa / enzymology
  • Mammals
  • Proteins / metabolism*
  • Selenium / deficiency
  • Selenium / metabolism*
  • Selenoproteins

Substances

  • Proteins
  • Selenoproteins
  • GPX2 protein, human
  • Glutathione Peroxidase
  • Selenium