Prostaglandin E2 Enhances Gap Junctional Intercellular Communication in Clonal Epithelial Cells

Int J Mol Sci. 2021 May 28;22(11):5813. doi: 10.3390/ijms22115813.

Abstract

Prostaglandins are a group of lipids that produce diverse physiological and pathological effects. Among them, prostaglandin E2 (PGE2) stands out for the wide variety of functions in which it participates. To date, there is little information about the influence of PGE2 on gap junctional intercellular communication (GJIC) in any type of tissue, including epithelia. In this work, we set out to determine whether PGE2 influences GJIC in epithelial cells (MDCK cells). To this end, we performed dye (Lucifer yellow) transfer assays to compare GJIC of MDCK cells treated with PGE2 and untreated cells. Our results indicated that (1) PGE2 induces a statistically significant increase in GJIC from 100 nM and from 15 min after its addition to the medium, (2) such effect does not require the synthesis of new mRNA or proteins subunits but rather trafficking of subunits already synthesized, and (3) such effect is mediated by the E2 receptor, which, in turn, triggers a signaling pathway that includes activation of adenylyl cyclase and protein kinase A (PKA). These results widen the knowledge regarding modulation of gap junctional intercellular communication by prostaglandins.

Keywords: dye transfer; epithelia; gap junction; prostaglandin E2.

MeSH terms

  • Adenylyl Cyclases / metabolism
  • Animals
  • Cell Communication / drug effects*
  • Cyclic AMP / metabolism
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Dinoprostone / pharmacology*
  • Dogs
  • Dose-Response Relationship, Drug
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects*
  • Epithelial Cells / metabolism
  • Gap Junctions / drug effects*
  • Gap Junctions / metabolism
  • Madin Darby Canine Kidney Cells
  • Receptors, Prostaglandin E, EP2 Subtype / metabolism
  • Signal Transduction / drug effects
  • Time Factors

Substances

  • Receptors, Prostaglandin E, EP2 Subtype
  • Cyclic AMP
  • Cyclic AMP-Dependent Protein Kinases
  • Adenylyl Cyclases
  • Dinoprostone

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