Medical Journals

Prostaglandin E2-ep4 Receptor Promotes Endothelial Cell Migration Via Erk Activation and Angiogenesis in Vivo.

Authors:
  • Rao Reena
  • Redha Reyadh
  • Macias-Perez Ines
  • Su Yan
  • Hao Chuanming
  • Zent Roy
  • Breyer Matthew D
  • Pozzi Ambra

From: Department of Medicine, Division of Nephrology, Vanderbilt University, Nashville, Tennessee 37232, USA.

The Journal of biological chemistry

  • Publish Date: Jun 2007
  • ISSN: 0021-9258
  • Volume: 282
  • Issue: 23
  • Pages: 16959-68
  • Medium: Print
  • Language: English
  • Citation (JAMA): Rao Reena, Redha Reyadh, Macias-Perez Ines, et al. Prostaglandin E2-ep4 Receptor Promotes Endothelial Cell Migration Via Erk Activation and Angiogenesis in Vivo.. J. Biol. Chem. Jun 2007;282:16959-68

Abstract

Prostaglandin E2 (PGE(2)), a major product of cyclooxygenase, exerts its functions by binding to four G protein-coupled receptors (EP1-4) and has been implicated in modulating angiogenesis. The present study examined the role of the EP4 receptor in regulating endothelial cell proliferation, migration, and tubulogenesis. Primary pulmonary microvascular endothelial cells were isolated from EP4(flox/flox) mice and were rendered null for the EP4 receptor with adenoCre virus. Whereas treatment with PGE(2) or the EP4 selective agonists PGE(1)-OH and ONO-AE1-329 induced migration, tubulogenesis, ERK activation and cAMP production in control adenovirus-transduced endothelial EP4(flox/flox) cells, no effects were seen in adenoCre-transduced EP4(flox/flox) cells. The EP4 agonist-induced endothelial cell migration was inhibited by ERK, but not PKA inhibitors, defining a functional link between PGE(2)-induced endothelial cell migration and EP4-mediated ERK signaling. Finally, PGE(2), as well as PGE(1)-OH and ONO-AE1-329, also promoted angiogenesis in an in vivo sponge assay providing evidence that the EP4 receptor mediates de novo vascularization in vivo.

Mesh Headings (Keywords): Animals, Base Sequence, Blotting, Western, Cell Movement, Cell Proliferation, Cells, Cultured, DNA Primers, Dinoprostone, Enzyme Activation, Extracellular Signal-Regulated MAP Kinases, Mice, Neovascularization, Physiologic, Receptors, Prostaglandin E, Reverse Transcriptase Polymerase Chain Reaction


Check for Full Text / PubMed Unique Identifier (PMID): 17401137


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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