Prostaglandin Receptor Signaling in Disease

Prostanoids, consisting of the prostaglandins (PGs) and the thromboxanes (TXs), are a group of lipid mediators formed in response to various stimuli. They include PGD2, PGE2, PGF2α, PGI2, and TXA2. They are released outside of the cells immediately after synthesis, and exert their actions by binding...

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Main Authors: Toshiyuki Matsuoka, Shuh Narumiya
Format: Article
Language:English
Published: Wiley 2007-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1100/tsw.2007.182
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author Toshiyuki Matsuoka
Shuh Narumiya
author_facet Toshiyuki Matsuoka
Shuh Narumiya
author_sort Toshiyuki Matsuoka
collection DOAJ
description Prostanoids, consisting of the prostaglandins (PGs) and the thromboxanes (TXs), are a group of lipid mediators formed in response to various stimuli. They include PGD2, PGE2, PGF2α, PGI2, and TXA2. They are released outside of the cells immediately after synthesis, and exert their actions by binding to a G-protein coupled rhodopsin-type receptor on the surface of target cells. There are eight types of the prostanoid receptors conserved in mammals from mouse to human. They are the PGD receptor (DP), four subtypes of the PGE receptor (EP1, EP2, EP3, and EP4), the PGF receptor (FP), PGI receptor (IP), and TXA receptor (TP). Recently, mice deficient in each of these prostanoid receptors were generated and subjected to various experimental models of disease. These studies have revealed the roles of PG receptor signaling in various pathological conditions, and suggest that selective manipulation of the prostanoid receptors may be beneficial in treatment of the pathological conditions. Here we review these recent findings of roles of prostanoid receptor signaling and their therapeutic implications.
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spelling doaj-art-0c762caf5a074c00a43d55bbf04c6fa92025-02-03T01:31:29ZengWileyThe Scientific World Journal1537-744X2007-01-0171329134710.1100/tsw.2007.182Prostaglandin Receptor Signaling in DiseaseToshiyuki Matsuoka0Shuh Narumiya1Department of Pharmacology, Faculty of Medicine, Kyoto University, Kyoto 606-8501, JapanDepartment of Pharmacology, Faculty of Medicine, Kyoto University, Kyoto 606-8501, JapanProstanoids, consisting of the prostaglandins (PGs) and the thromboxanes (TXs), are a group of lipid mediators formed in response to various stimuli. They include PGD2, PGE2, PGF2α, PGI2, and TXA2. They are released outside of the cells immediately after synthesis, and exert their actions by binding to a G-protein coupled rhodopsin-type receptor on the surface of target cells. There are eight types of the prostanoid receptors conserved in mammals from mouse to human. They are the PGD receptor (DP), four subtypes of the PGE receptor (EP1, EP2, EP3, and EP4), the PGF receptor (FP), PGI receptor (IP), and TXA receptor (TP). Recently, mice deficient in each of these prostanoid receptors were generated and subjected to various experimental models of disease. These studies have revealed the roles of PG receptor signaling in various pathological conditions, and suggest that selective manipulation of the prostanoid receptors may be beneficial in treatment of the pathological conditions. Here we review these recent findings of roles of prostanoid receptor signaling and their therapeutic implications.http://dx.doi.org/10.1100/tsw.2007.182
spellingShingle Toshiyuki Matsuoka
Shuh Narumiya
Prostaglandin Receptor Signaling in Disease
The Scientific World Journal
title Prostaglandin Receptor Signaling in Disease
title_full Prostaglandin Receptor Signaling in Disease
title_fullStr Prostaglandin Receptor Signaling in Disease
title_full_unstemmed Prostaglandin Receptor Signaling in Disease
title_short Prostaglandin Receptor Signaling in Disease
title_sort prostaglandin receptor signaling in disease
url http://dx.doi.org/10.1100/tsw.2007.182
work_keys_str_mv AT toshiyukimatsuoka prostaglandinreceptorsignalingindisease
AT shuhnarumiya prostaglandinreceptorsignalingindisease