ADP受容体、ADPレセプター
- 関
- ATP receptor、P2 purinoceptor、purinergic P2 receptor
WordNet
- the 1st letter of the Roman alphabet (同)a
- the blood group whose red cells carry the A antigen (同)type_A, group A
- a cellular structure that is postulated to exist in order to mediate between a chemical agent that acts on nervous tissue and the physiological response
- in the Christian era; used before dates after the supposed year Christ was born; "in AD 200" (同)A.D., anno_Domini
PrepTutorEJDIC
- answer / ampere
- =sense organ / 受信装置
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/01/20 17:12:53」(JST)
[Wiki en表示]
P2Y receptors are a family of purinergic G protein-coupled receptors, stimulated by nucleotides such as ATP, ADP, UTP, UDP and UDP-glucose. To date, 12 P2Y receptors have been cloned in humans: P2Y1, P2Y2, P2Y4, P2Y5, P2Y6, P2Y8, P2Y9 (present in NCBI as GPR23), P2Y10, P2Y11, P2Y12, P2Y13 and P2Y14.[1]
P2Y receptors are present in almost all human tissues where they exert various biological functions based on their G-protein coupling.
Contents
- 1 Coupling
- 2 Clinical significance
- 3 References
- 4 External links
Coupling[edit]
The biological effects of P2Y receptor activation depends on how they couple to downstream signalling pathways, either via Gi, Gq/11 or Gs G proteins. Human P2Y receptors have the following G protein coupling:
Protein |
Gene |
Coupling |
Nucleotide |
P2RY1 |
P2RY1 |
Gq/11 |
ADP |
P2RY2 |
P2RY2 |
Gq/11 |
ATP, UTP |
P2RY4 |
P2RY4 |
Gi and Gq/11 |
UTP |
P2RY5 / LPA6 |
LPAR6 |
|
Lysophosphatidic acid[2] |
P2RY6 |
P2RY6 |
Gq/11 |
UDP |
P2RY8 |
P2RY8 |
|
orphan receptor |
P2RY9 / LPAR4 / GPR23 |
LPAR4 |
|
Lysophosphatidic acid |
P2RY10 |
P2RY10 |
|
orphan receptor |
P2RY11 |
P2RY11 |
Gs and Gq/11 |
ATP |
P2RY12 |
P2RY12 |
Gi |
ADP |
P2RY13 |
P2RY13 |
Gi |
ADP |
P2RY14 |
P2RY14 |
Gi |
UDP-glucose |
The gaps in P2Y receptor numbering is due to that several receptors (P2Y3, P2Y5, P2Y7, P2Y8, P2Y9, P2Y10) were thought to be P2Y receptors when they were cloned, when in fact they are not.
Clinical significance[edit]
- P2Y2 is a potential drug target for treating cystic fibrosis.[3]
- P2Y11 is a regulator of immune response, and a common polymorphism carried by almost 20% of North European caucasians give increased risk of myocardial infarction, making P2Y11 an interesting drug target candidate for treatment of myocardial infarction.[4]
- P2Y12 is the target of the anti-platelet drug clopidogrel[5] and other thienopyridines.
References[edit]
- ^ Abbracchio MP, Burnstock G, Boeynaems JM, Barnard EA, Boyer JL, Kennedy C, Knight GE, Fumagalli M, Gachet C, Jacobson KA, Weisman GA (2006). "International Union of Pharmacology LVIII: update on the P2Y G protein-coupled nucleotide receptors: from molecular mechanisms and pathophysiology to therapy". Pharmacol. Rev. 58 (3): 281–341. doi:10.1124/pr.58.3.3. PMID 16968944.
- ^ Pasternack SM, von Kügelgen I, Aboud KA, Lee YA, Rüschendorf F, Voss K, Hillmer AM, Molderings GJ, Franz T, Ramirez A, Nürnberg P, Nöthen MM, Betz RC. "G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth." Nature Genetics 2008 Mar;40(3):329-34. PMID 18297070
- ^ Kellerman D, Evans R, Mathews D, Shaffer C (2002). "Inhaled P2Y2 receptor agonists as a treatment for patients with Cystic Fibrosis lung disease". Adv. Drug Deliv. Rev. 54 (11): 1463–74. doi:10.1016/S0169-409X(02)00154-0. PMID 12458155.
- ^ Amisten S, Melander O, Wihlborg AK, Berglund G, Erlinge D (2007). "Increased risk of acute myocardial infarction and elevated levels of C-reactive protein in carriers of the Thr-87 variant of the ATP receptor P2Y11". Eur. Heart J. 28 (1): 13–8. doi:10.1093/eurheartj/ehl410. PMID 17135283.
- ^ Herbert JM, Savi P (2003). "P2Y12, a new platelet ADP receptor, target of clopidogrel". Seminars in vascular medicine 3 (2): 113–22. doi:10.1055/s-2003-40669. PMID 15199474.
External links[edit]
- Ivar von Kügelgen: Pharmacology of mammalian P2X- and P2Y-receptors, BIOTREND Reviews No. 03, September 2008,© 2008 BIOTREND Chemicals AG
- "P2Y Receptors". IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology.
- Purinergic P2 receptors at the US National Library of Medicine Medical Subject Headings (MeSH)
Cell surface receptor: G protein-coupled receptors
|
|
Class A:
Rhodopsin like |
|
|
Class B: Secretin like |
Orphan
|
- GPR (56
- 64
- 97
- 98
- 110
- 111
- 112
- 113
- 114
- 115
- 116
- 123
- 124
- 125
- 126
- 128
- 133
- 143
- 144
- 155
- 157)
|
|
Other
|
- Brain-specific angiogenesis inhibitor (1
- 2
- 3)
- Cadherin (1
- 2
- 3)
- Calcitonin
- CALCRL
- CD97
- Corticotropin-releasing hormone (1
- 2)
- EMR (1
- 2
- 3)
- Glucagon (GR
- GIPR
- GLP1R
- GLP2R)
- Growth hormone releasing hormone
- PACAPR1
- GPR
- Latrophilin (1
- 2
- 3
- ELTD1)
- Methuselah-like proteins
- Parathyroid hormone (1
- 2)
- Secretin
- Vasoactive intestinal peptide (1
- 2)
|
|
|
Class C: Metabotropic
glutamate / pheromone |
Taste
|
- TAS1R (1
- 2
- 3)
- TAS2R (1
- 3
- 4
- 5
- 7
- 8
- 9
- 10
- 13
- 14
- 16
- 19
- 20
- 30
- 31
- 38
- 39
- 40
- 41
- 42
- 43
- 45
- 46
- 50
- 60)
|
|
Other
|
- Calcium-sensing receptor
- GABA B (1
- 2)
- Glutamate receptor (Metabotropic glutamate (1
- 2
- 3
- 4
- 5
- 6
- 7
- 8))
- GPRC6A
- GPR (156
- 158
- 179)
- RAIG (1
- 2
- 3
- 4)
|
|
|
Class F:
Frizzled / Smoothened |
Frizzled
|
- Frizzled (1
- 2
- 3
- 4
- 5
- 6
- 7
- 8
- 9
- 10)
|
|
Smoothened
|
|
|
|
B trdu: iter (nrpl/grfl/cytl/horl), csrc (lgic, enzr, gprc, igsr, intg, nrpr/grfr/cytr), itra (adap, gbpr, mapk), calc, lipd; path (hedp, wntp, tgfp+mapp, notp, jakp, fsap, hipp, tlrp)
|
|
UpToDate Contents
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English Journal
- P2Y1 receptor inhibits GABA transport through a calcium signalling-dependent mechanism in rat cortical astrocytes.
- Jacob PF1, Vaz SH, Ribeiro JA, Sebastião AM.
- Glia.Glia.2014 Aug;62(8):1211-26. doi: 10.1002/glia.22673. Epub 2014 Apr 15.
- Astrocytes express a variety of purinergic (P2) receptors, involved in astrocytic communication through fast increases in [Ca(2+) ]i . Of these, the metabotropic ATP receptors (P2Y) regulate cytoplasmic Ca(2+) levels through the PLC-PKC pathway. GABA transporters are a substrate for a number of Ca(2
- PMID 24733747
- LL-202, a newly synthesized flavonoid, inhibits tumor growth via inducing G2/M phase arrest and cell apoptosis in MCF-7 human breast cancer cells in vitro and in vivo.
- Tao L1, Fu R2, Wang X2, Yao J2, Zhou Y2, Dai Q2, Li Z3, Lu N2, Wang W4.
- Toxicology letters.Toxicol Lett.2014 Jul 3;228(1):1-12. doi: 10.1016/j.toxlet.2014.04.002. Epub 2014 Apr 19.
- We recently established that LL-202, a newly synthesized flavonoid, exhibited obvious anticancer effects against human breast cells in vivo and in vitro. The underlying mechanism of its anticancer activity remains to be elucidated. In this study, we demonstrated that LL-202 inhibited the growth and
- PMID 24752227
- Colistin-Induced Nephrotoxicity in Mice Involves the Mitochondrial, Death Receptor, and Endoplasmic Reticulum Pathways.
- Dai C1, Li J2, Tang S1, Li J3, Xiao X4.
- Antimicrobial agents and chemotherapy.Antimicrob Agents Chemother.2014 Jul;58(7):4075-4085. Epub 2014 May 5.
- Nephrotoxicity is the dose-limiting factor for colistin, but the exact mechanism is unknown. This study aimed to investigate the roles of the mitochondrial, death receptor, and endoplasmic reticulum pathways in colistin-induced nephrotoxicity. Mice were intravenously administered 7.5 or 15 mg of col
- PMID 24798292
Japanese Journal
- Delineation of Platelet Activation Pathway of Scutellarein Revealed Its Intracellular Target as Protein Kinase C
- プリン受容体ヘテロ多量体形成が血小板機能に与える影響の解析
Related Links
- The initial response to ADP is a change in the shape of the platelet whereby disc shaped cells convert into a spherical form from which pseudopodia emerge. This change, which is mediated by the P2Y 1 receptor ...
- 1. Cochrane Database Syst Rev. 2012 Nov 14;11:CD005449. doi: 10.1002/14651858.CD005449.pub2. Adenosine-diphosphate (ADP) receptor antagonists for the prevention of cardiovascular disease in type 2 diabetes ...
★リンクテーブル★
[★]
- 関
- ADP receptor、ATP receptor、P2 purinergic receptor、P2 purinoceptor、P2 receptor
[★]
- 関
- ADP receptor、ATP receptor、P2 purinergic receptor、P2 receptor、purinergic P2 receptor
[★]
- 英
- ADP receptor
- 関
- ATP受容体、プリンP2受容体、P2プリン受容体、ADPレセプター
[★]
- 関
- ADP receptor、P2 purinoceptor、purinergic P2 receptor
[★]
- 英
- ADP receptor
- 関
- ADP受容体
[★]
[★]
[★]