GPR132, G protein-spregnuti receptor 132, je protein koji je kod čoveka kodiran GPR132genom.[1][2]
GPR132 je receptor visokog afiniteta za lizofosfatidilholin (LPC), jednu od fosfolipidnih komponenti oksidovanih lipoproteina niske gustine. Ovaj protein može da reaguje na promenu LPC nivoa na mestima zapaljenja i da ograniči ekspanziju ćelija ćelija koje infiltriraju tkivo. Sličan protein kod miša učestvuje u progresiji ćelijskog cilusa.[2]
↑Le LQ, Kabarowski JH, Wong S, Nguyen K, Gambhir SS, Witte ON (Jun 2002). „Positron emission tomography imaging analysis of G2A as a negative modifier of lymphoid leukemogenesis initiated by the BCR-ABL oncogene”. Cancer Cell1 (4): 381–91. DOI:10.1016/S1535-6108(02)00058-2. PMID12086852.
↑ 2,02,1„Entrez Gene: GPR132 G protein-coupled receptor 132”. PMID29933.
Kabarowski JH, Zhu K, Le LQ, et al. (2001). „Lysophosphatidylcholine as a ligand for the immunoregulatory receptor G2A.”. Science293 (5530): 702–5. DOI:10.1126/science.1061781. PMID11474113.
Lin P, Ye RD (2003). „The lysophospholipid receptor G2A activates a specific combination of G proteins and promotes apoptosis.”. J. Biol. Chem.278 (16): 14379–86. DOI:10.1074/jbc.M209101200. PMID12586833.
Lum H, Qiao J, Walter RJ, et al. (2003). „Inflammatory stress increases receptor for lysophosphatidylcholine in human microvascular endothelial cells.”. Am. J. Physiol. Heart Circ. Physiol.285 (4): H1786–9. DOI:10.1152/ajpheart.00359.2003. PMID12805023.
Murakami N, Yokomizo T, Okuno T, Shimizu T (2004). „G2A is a proton-sensing G-protein-coupled receptor antagonized by lysophosphatidylcholine.”. J. Biol. Chem.279 (41): 42484–91. DOI:10.1074/jbc.M406561200. PMID15280385.
Obinata H, Hattori T, Nakane S, et al. (2006). „Identification of 9-hydroxyoctadecadienoic acid and other oxidized free fatty acids as ligands of the G protein-coupled receptor G2A.”. J. Biol. Chem.280 (49): 40676–83. DOI:10.1074/jbc.M507787200. PMID16236715.
Frasch SC, Zemski-Berry K, Murphy RC, et al. (2007). „Lysophospholipids of different classes mobilize neutrophil secretory vesicles and induce redundant signaling through G2A.”. J. Immunol.178 (10): 6540–8. PMID17475884.