EP1 receptor
(Preusmjereno sa stranice PTGER1)
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| Prostaglandinski E receptor 1 | |||||||||||
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| Identifikatori | |||||||||||
| Simboli | PTGER1; EP1 | ||||||||||
| Vanjski ID | OMIM: 176802 MGI: 97793 HomoloGene: 738 IUPHAR: EP1 GeneCards: PTGER1 Gene | ||||||||||
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| Pregled RNK izražavanja | |||||||||||
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| podaci | |||||||||||
| Ortolozi | |||||||||||
| Vrsta | Čovek | Miš | |||||||||
| Entrez | 5731 | 19216 | |||||||||
| Ensembl | ENSG00000160951 | ENSMUSG00000019464 | |||||||||
| UniProt | P34995 | P35375 | |||||||||
| RefSeq (mRNA) | NM_000955.2 | NM_013641.2 | |||||||||
| RefSeq (protein) | NP_000946.2 | NP_038669.1 | |||||||||
| Lokacija (UCSC) | Chr 19: 14.58 - 14.59 Mb | Chr 8: 86.19 - 86.2 Mb | |||||||||
| PubMed pretraga | [1] | [2] | |||||||||
Prostaglandinski E receptor 1 (podtip EP1) je prostaglandinski receptor. PTGER1 je njegov ljudski gen.[1]
Ovaj protein je član familije G protein spregnutih receptora. On je jedan od četiri receptora identifikovana za prostaglandin E2 (PGE2). Gq proteini posreduju aktivnost ovog receptora putem sistema fosfatidilinozitol-kalcijum sekundarnog glasnika. Ispitivanja na nokaut miševima sugeriraju da ovaj receptor posreduje algeziju, i učestvuje u regulaciji krvnog pritiska. Studije na miševima takođe pokazuju da ovaj gen posreduje adrenokortikotropni hormonski respons na bakterijski endotoksin.[1]
- Coleman RA, Smith WL, Narumiya S (1994). „International Union of Pharmacology classification of prostanoid receptors: properties, distribution, and structure of the receptors and their subtypes.”. Pharmacol. Rev. 46 (2): 205–29. PMID 7938166.
- Lee TY, Watanabe Y (1975). „A nonlinear regression model as applied to the comparison of axis-angles of electrocardiographic systems.”. Japanese heart journal 16 (3): 243–56. PMID 1160156.
- Duncan AM, Anderson LL, Funk CD, et al. (1995). „Chromosomal localization of the human prostanoid receptor gene family.”. Genomics 25 (3): 740–2. DOI:10.1016/0888-7543(95)80022-E. PMID 7759114.
- Funk CD, Furci L, FitzGerald GA, et al. (1994). „Cloning and expression of a cDNA for the human prostaglandin E receptor EP1 subtype.”. J. Biol. Chem. 268 (35): 26767–72. PMID 8253813.
- Kurihara Y, Endo H, Kondo H (2001). „Induction of IL-6 via the EP3 subtype of prostaglandin E receptor in rat adjuvant-arthritic synovial cells.”. Inflamm. Res. 50 (1): 1–5. DOI:10.1007/s000110050716. PMID 11235015.
- Kyveris A, Maruscak E, Senchyna M (2002). „Optimization of RNA isolation from human ocular tissues and analysis of prostanoid receptor mRNA expression using RT-PCR.”. Mol. Vis. 8: 51–8. PMID 11951086.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). „Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. DOI:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Matsuoka Y, Furuyashiki T, Bito H, et al. (2003). „Impaired adrenocorticotropic hormone response to bacterial endotoxin in mice deficient in prostaglandin E receptor EP1 and EP3 subtypes.”. Proc. Natl. Acad. Sci. U.S.A. 100 (7): 4132–7. DOI:10.1073/pnas.0633341100. PMC 153060. PMID 12642666.
- Richards JA, Brueggemeier RW (2003). „Prostaglandin E2 regulates aromatase activity and expression in human adipose stromal cells via two distinct receptor subtypes.”. J. Clin. Endocrinol. Metab. 88 (6): 2810–6. DOI:10.1210/jc.2002-021475. PMID 12788892.
- Kitamura T, Itoh M, Noda T, et al. (2004). „Combined effects of prostaglandin E receptor subtype EP1 and subtype EP4 antagonists on intestinal tumorigenesis in adenomatous polyposis coli gene knockout mice.”. Cancer Sci. 94 (7): 618–21. DOI:10.1111/j.1349-7006.2003.tb01492.x. PMID 12841871.
- Moreland RB, Kim N, Nehra A, et al. (2004). „Functional prostaglandin E (EP) receptors in human penile corpus cavernosum.”. Int. J. Impot. Res. 15 (5): 362–8. DOI:10.1038/sj.ijir.3901042. PMID 14562138.
- Su JL, Shih JY, Yen ML, et al. (2004). „Cyclooxygenase-2 induces EP1- and HER-2/Neu-dependent vascular endothelial growth factor-C up-regulation: a novel mechanism of lymphangiogenesis in lung adenocarcinoma.”. Cancer Res. 64 (2): 554–64. DOI:10.1158/0008-5472.CAN-03-1301. PMID 14744769.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). „The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).”. Genome Res. 14 (10B): 2121–7. DOI:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Han C, Wu T (2005). „Cyclooxygenase-2-derived prostaglandin E2 promotes human cholangiocarcinoma cell growth and invasion through EP1 receptor-mediated activation of the epidermal growth factor receptor and Akt.”. J. Biol. Chem. 280 (25): 24053–63. DOI:10.1074/jbc.M500562200. PMID 15855163.
- Nicola C, Timoshenko AV, Dixon SJ, et al. (2005). „EP1 receptor-mediated migration of the first trimester human extravillous trophoblast: the role of intracellular calcium and calpain.”. J. Clin. Endocrinol. Metab. 90 (8): 4736–46. DOI:10.1210/jc.2005-0413. PMID 15886234.
- Han C, Michalopoulos GK, Wu T (2006). „Prostaglandin E2 receptor EP1 transactivates EGFR/MET receptor tyrosine kinases and enhances invasiveness in human hepatocellular carcinoma cells.”. J. Cell. Physiol. 207 (1): 261–70. DOI:10.1002/jcp.20560. PMID 16331686.
- Durrenberger PF, Facer P, Casula MA, et al. (2006). „Prostanoid receptor EP1 and Cox-2 in injured human nerves and a rat model of nerve injury: a time-course study.”. BMC neurology 6: 1. DOI:10.1186/1471-2377-6-1. PMC 1361784. PMID 16393343.
- McGraw DW, Mihlbachler KA, Schwarb MR, et al. (2006). „Airway smooth muscle prostaglandin-EP1 receptors directly modulate beta2-adrenergic receptors within a unique heterodimeric complex.”. J. Clin. Invest. 116 (5): 1400–9. DOI:10.1172/JCI25840. PMC 1451203. PMID 16670773.
- Horita H, Kuroda E, Hachisuga T, et al. (2007). „Induction of prostaglandin E2 production by leukemia inhibitory factor promotes migration of first trimester extravillous trophoblast cell line, HTR-8/SVneo.”. Hum. Reprod. 22 (7): 1801–9. DOI:10.1093/humrep/dem125. PMID 17525067.
- „Prostanoid Receptors: EP1”. IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology. Arhivirano iz originala na datum 2016-03-03.