| http://purl.uniprot.org/citations/19389848 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/19389848 | http://www.w3.org/2000/01/rdf-schema#comment | "Macula densa (MD) cells of the juxtaglomerular apparatus (JGA) are salt sensors and generate paracrine signals that control renal blood flow, glomerular filtration, and release of the prohypertensive hormone renin. We hypothesized that the recently identified succinate receptor GPR91 is present in MD cells and regulates renin release. Using immunohistochemistry, we identified GPR91 in the apical plasma membrane of MD cells. Treatment of MD cells with succinate activated mitogen-activated protein kinases (MAPKs; p38 and extracellular signal-regulated kinases 1/2) and cyclooxygenase 2 (COX-2) and induced the synthesis and release of prostaglandin E(2), a potent vasodilator and classic paracrine mediator of renin release. Using microperfused JGA and real-time confocal fluorescence imaging of quinacrine-labeled renin granules, we detected significant renin release in response to tubular succinate (EC(50) 350 microM). Genetic deletion of GPR91 (GPR91(-/-) mice) or pharmacologic inhibition of MAPK or COX-2 blocked succinate-induced renin release. Streptozotocin-induced diabetes caused GPR91-dependent upregulation of renal cortical phospho-p38, extracellular signal-regulated kinases 1/2, COX-2, and renin content. Salt depletion for 1 wk increased plasma renin activity seven-fold in wild-type mice but only 3.4-fold in GPR91(-/-) mice. In summary, MD cells can sense alterations in local tissue metabolism via accumulation of tubular succinate and GPR91 signaling, which involves the activation of MAPKs, COX-2, and the release of prostaglandin E(2). This mechanism may be integral in the regulation of renin release and activation of the renin-angiotensin system in health and disease."xsd:string |
| http://purl.uniprot.org/citations/19389848 | http://purl.org/dc/terms/identifier | "doi:10.1681/asn.2008070740"xsd:string |
| http://purl.uniprot.org/citations/19389848 | http://purl.uniprot.org/core/author | "Peti-Peterdi J."xsd:string |
| http://purl.uniprot.org/citations/19389848 | http://purl.uniprot.org/core/author | "Kang J.J."xsd:string |
| http://purl.uniprot.org/citations/19389848 | http://purl.uniprot.org/core/author | "Toma I."xsd:string |
| http://purl.uniprot.org/citations/19389848 | http://purl.uniprot.org/core/author | "Meer E.J."xsd:string |
| http://purl.uniprot.org/citations/19389848 | http://purl.uniprot.org/core/author | "Vargas S.L."xsd:string |
| http://purl.uniprot.org/citations/19389848 | http://purl.uniprot.org/core/date | "2009"xsd:gYear |
| http://purl.uniprot.org/citations/19389848 | http://purl.uniprot.org/core/name | "J Am Soc Nephrol"xsd:string |
| http://purl.uniprot.org/citations/19389848 | http://purl.uniprot.org/core/pages | "1002-1011"xsd:string |
| http://purl.uniprot.org/citations/19389848 | http://purl.uniprot.org/core/title | "Activation of the succinate receptor GPR91 in macula densa cells causes renin release."xsd:string |
| http://purl.uniprot.org/citations/19389848 | http://purl.uniprot.org/core/volume | "20"xsd:string |
| http://purl.uniprot.org/citations/19389848 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/19389848 |
| http://purl.uniprot.org/citations/19389848 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/19389848 |
| http://purl.uniprot.org/uniprot/#_Q99MT6-mappedCitation-19389848 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/19389848 |
| http://purl.uniprot.org/uniprot/Q99MT6 | http://purl.uniprot.org/core/mappedCitation | http://purl.uniprot.org/citations/19389848 |