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Oncotarget. 2017 Nov 23;9(1):539-552. doi: 10.18632/oncotarget.22640. eCollection 2018 Jan 2.

Loss of epithelium-specific GPx2 results in aberrant cell fate decisions during intestinal differentiation.

Author information

1
Institute of Medical Immunology, Martin Luther University Halle-Wittenberg, 06112 Halle (Saale), Germany.
2
Institute of Pathology, Martin Luther University Halle-Wittenberg, 06112 Halle (Saale), Germany.
3
Delacon Biotechnik GmbH, 4221 Steyregg, Austria.
4
Department of Bioorganic Chemistry, Leibniz-Institute of Plant Biochemistry, 06120 Halle (Saale), Germany.
5
Institute of Nutrition, Friedrich Schiller University Jena, 07743 Jena, Germany.

Abstract

The selenoprotein glutathione peroxidase 2 (GPx2) is expressed in the epithelium of the gastrointestinal tract, where it is thought to be involved in maintaining mucosal homeostasis. To gain novel insights into the role of GPx2, proteomic profiles of colonic tissues either derived from wild type (WT) or GPx2 knockout (KO) mice, maintained under selenium (Se) deficiency or adequate Se supplementation conditions were established and analyzed. Amongst the panel of differentially expressed proteins, the calcium-activated chloride channel regulator 1 (CLCA1) was significantly down-regulated in GPx2 KO versus WT mice regardless of the given Se status. Moreover, transcript levels of the isoforms CLCA2 and CLCA3 showed a similar expression pattern. In the intestine, CLCA1 is usually restricted to mucin-producing goblet cells. However, although -SeKO mice had the highest numbers of goblet cells as confirmed by significantly enhanced mRNA expression levels of the goblet cell marker mucin-2, the observed expression pattern suggests that GPx2 KO goblet cells might be limited in synthesizing CLCA1. Furthermore, transcript levels of differentiation markers such as chromogranin-1 (Chga) for enteroendocrine cells and leucine-rich repeat-containing G-protein coupled receptor 5 (Lgr5) for stem cells were also downregulated in GPx2 KO mice. Moreover, this was accompanied by a downregulation of the mRNA expression levels of the intestinal hormones glucagon-like peptide 1 (Glp1), ghrelin (Ghrl) and somatostatin (Sst). Thus, it seems that GPx2 might be important for the modulation of cell fate decisions in the murine intestinal epithelium.

KEYWORDS:

Clca1; DIGE; glutathione peroxidase 2; selenium; stem cells

Conflict of interest statement

CONFLICTS OF INTEREST The authors would like to state that they have no potential conflicts of interest to report.

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