Sphingosine-1-phosphate regulates RGS2 and RGS16 mRNA expression in vascular smooth muscle cells

Regulator of G protein signalling (RGS) protein expression is altered under growth promoting conditions in vascular smooth muscle cells (VSMCs). Since sphingosine-1-phosphate (S1P) is an important growth stimulatory factor, we investigated whether stimulation of VSMCs with S1P results in alterations...

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Veröffentlicht in:European journal of pharmacology 2009-03, Vol.606 (1), p.25-31
Hauptverfasser: Hendriks-Balk, Mariëlle C., Hajji, Najat, van Loenen, Pieter B., Michel, Martin C., Peters, Stephan L.M., Alewijnse, Astrid E.
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container_end_page 31
container_issue 1
container_start_page 25
container_title European journal of pharmacology
container_volume 606
creator Hendriks-Balk, Mariëlle C.
Hajji, Najat
van Loenen, Pieter B.
Michel, Martin C.
Peters, Stephan L.M.
Alewijnse, Astrid E.
description Regulator of G protein signalling (RGS) protein expression is altered under growth promoting conditions in vascular smooth muscle cells (VSMCs). Since sphingosine-1-phosphate (S1P) is an important growth stimulatory factor, we investigated whether stimulation of VSMCs with S1P results in alterations in mRNA expression levels of several RGS proteins and which signalling components are involved. VSMCs were stimulated with S1P and mRNA expression levels of RGS2, RGS3, RGS4, RGS5 and RGS16 were measured by real-time polymerase chain reaction. S1P caused a time-dependent up-regulation of RGS2 and RGS16 mRNA expression. FTY720-P, a S1P 1/S1P 3–5 agonist, did not regulate RGS2 mRNA levels although it did up-regulate RGS16 mRNA expression. Pertussis toxin treatment revealed that the S1P-induced RGS16 expression was G i/o-dependent whereas up-regulation of RGS2 mRNA was not. Phosphatidylinositol 3-kinase, protein kinase C and mitogen-activated protein kinase kinase apparently were not involved in the S1P-induced up-regulation of both RGS proteins. The present study demonstrates that S1P induces RGS2 and RGS16 mRNA expression but uses distinct S1P receptor subtypes and signalling pathways to regulate expression of these RGS proteins.
doi_str_mv 10.1016/j.ejphar.2009.01.018
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Since sphingosine-1-phosphate (S1P) is an important growth stimulatory factor, we investigated whether stimulation of VSMCs with S1P results in alterations in mRNA expression levels of several RGS proteins and which signalling components are involved. VSMCs were stimulated with S1P and mRNA expression levels of RGS2, RGS3, RGS4, RGS5 and RGS16 were measured by real-time polymerase chain reaction. S1P caused a time-dependent up-regulation of RGS2 and RGS16 mRNA expression. FTY720-P, a S1P 1/S1P 3–5 agonist, did not regulate RGS2 mRNA levels although it did up-regulate RGS16 mRNA expression. Pertussis toxin treatment revealed that the S1P-induced RGS16 expression was G i/o-dependent whereas up-regulation of RGS2 mRNA was not. Phosphatidylinositol 3-kinase, protein kinase C and mitogen-activated protein kinase kinase apparently were not involved in the S1P-induced up-regulation of both RGS proteins. 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Drug treatments</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, Lysosphingolipid - metabolism</topic><topic>Regulator of G protein signalling</topic><topic>RGS Proteins - genetics</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Signal Transduction - drug effects</topic><topic>Sphingosine - analogs &amp; derivatives</topic><topic>Sphingosine - metabolism</topic><topic>Sphingosine - pharmacology</topic><topic>Sphingosine-1-phosphate receptor</topic><topic>Up-Regulation - drug effects</topic><topic>VSMC</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hendriks-Balk, Mariëlle C.</creatorcontrib><creatorcontrib>Hajji, Najat</creatorcontrib><creatorcontrib>van Loenen, Pieter B.</creatorcontrib><creatorcontrib>Michel, Martin C.</creatorcontrib><creatorcontrib>Peters, Stephan L.M.</creatorcontrib><creatorcontrib>Alewijnse, Astrid E.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hendriks-Balk, Mariëlle C.</au><au>Hajji, Najat</au><au>van Loenen, Pieter B.</au><au>Michel, Martin C.</au><au>Peters, Stephan L.M.</au><au>Alewijnse, Astrid E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sphingosine-1-phosphate regulates RGS2 and RGS16 mRNA expression in vascular smooth muscle cells</atitle><jtitle>European journal of pharmacology</jtitle><addtitle>Eur J Pharmacol</addtitle><date>2009-03-15</date><risdate>2009</risdate><volume>606</volume><issue>1</issue><spage>25</spage><epage>31</epage><pages>25-31</pages><issn>0014-2999</issn><eissn>1879-0712</eissn><coden>EJPHAZ</coden><abstract>Regulator of G protein signalling (RGS) protein expression is altered under growth promoting conditions in vascular smooth muscle cells (VSMCs). Since sphingosine-1-phosphate (S1P) is an important growth stimulatory factor, we investigated whether stimulation of VSMCs with S1P results in alterations in mRNA expression levels of several RGS proteins and which signalling components are involved. VSMCs were stimulated with S1P and mRNA expression levels of RGS2, RGS3, RGS4, RGS5 and RGS16 were measured by real-time polymerase chain reaction. S1P caused a time-dependent up-regulation of RGS2 and RGS16 mRNA expression. FTY720-P, a S1P 1/S1P 3–5 agonist, did not regulate RGS2 mRNA levels although it did up-regulate RGS16 mRNA expression. Pertussis toxin treatment revealed that the S1P-induced RGS16 expression was G i/o-dependent whereas up-regulation of RGS2 mRNA was not. Phosphatidylinositol 3-kinase, protein kinase C and mitogen-activated protein kinase kinase apparently were not involved in the S1P-induced up-regulation of both RGS proteins. The present study demonstrates that S1P induces RGS2 and RGS16 mRNA expression but uses distinct S1P receptor subtypes and signalling pathways to regulate expression of these RGS proteins.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>19374869</pmid><doi>10.1016/j.ejphar.2009.01.018</doi><tpages>7</tpages></addata></record>
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subjects Animals
Biological and medical sciences
FTY720-P
Gene Expression Regulation - drug effects
Lysophospholipids - metabolism
Lysophospholipids - pharmacology
Male
Medical sciences
Muscle, Smooth, Vascular - cytology
Muscle, Smooth, Vascular - drug effects
Muscle, Smooth, Vascular - metabolism
Pharmacology. Drug treatments
Rats
Rats, Wistar
Receptors, Lysosphingolipid - metabolism
Regulator of G protein signalling
RGS Proteins - genetics
RNA, Messenger - genetics
RNA, Messenger - metabolism
Signal Transduction - drug effects
Sphingosine - analogs & derivatives
Sphingosine - metabolism
Sphingosine - pharmacology
Sphingosine-1-phosphate receptor
Up-Regulation - drug effects
VSMC
title Sphingosine-1-phosphate regulates RGS2 and RGS16 mRNA expression in vascular smooth muscle cells
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