Dicer1 ablation in the mouse epididymis causes dedifferentiation of the epithelium and imbalance in sex steroid signaling

PLoS One. 2012;7(6):e38457. doi: 10.1371/journal.pone.0038457. Epub 2012 Jun 6.

Abstract

Background: The postnatal development of the epididymis is a complex process that results in a highly differentiated epithelium, divided into several segments. Recent studies indicate a role for RNA interference (RNAi) in the development of the epididymis, however, the actual requirement for RNAi has remained elusive. Here, we present the first evidence of a direct need for RNAi in the differentiation of the epididymal epithelium.

Methodology/principal findings: By utilizing the Cre-LoxP system we have generated a conditional knock-out of Dicer1 in the two most proximal segments of the mouse epididymis. Recombination of Dicer1, catalyzed by Defb41(iCre/wt), took place before puberty, starting from 12 days postpartum. Shortly thereafter, downregulation of the expression of two genes specific for the most proximal epididymis (lipocalin 8 and cystatin 8) was observed. Following this, segment development continued until week 5 at which age the epithelium started to regress back to an undifferentiated state. The dedifferentiated epithelium also showed an increase in estrogen receptor 1 expression while the expression of androgen receptor and its target genes; glutathione peroxidase 5, lipocalin 5 and cysteine-rich secretory protein 1 was downregulated, indicating imbalanced sex steroid signaling.

Conclusions/significance: At the time of the final epididymal development, Dicer1 acts as a regulator of signaling pathways essential for maintaining epithelial cell differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Cell Dedifferentiation / physiology*
  • Cystatins / metabolism
  • DEAD-box RNA Helicases / deficiency*
  • DEAD-box RNA Helicases / genetics
  • Epididymis / cytology
  • Epididymis / growth & development*
  • Epididymis / metabolism
  • Epithelial Cells / physiology*
  • Estrogen Receptor alpha / metabolism
  • Gene Expression Regulation, Developmental / physiology*
  • Gene Knockout Techniques
  • Gonadal Steroid Hormones / metabolism*
  • Histological Techniques
  • Immunohistochemistry
  • Lipocalins / metabolism
  • Male
  • Mice
  • RNA Interference
  • Receptors, Androgen / metabolism
  • Ribonuclease III / deficiency*
  • Ribonuclease III / genetics
  • Signal Transduction / genetics*
  • beta-Defensins / metabolism

Substances

  • Cystatins
  • Estrogen Receptor alpha
  • Gonadal Steroid Hormones
  • Lcn8 protein, mouse
  • Lipocalins
  • Receptors, Androgen
  • beta-Defensins
  • Cst8 protein, mouse
  • Dicer1 protein, mouse
  • Ribonuclease III
  • DEAD-box RNA Helicases