| Part of a series on |
| Purinergic signalling |
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Simplified illustration of extracellular purinergic signalling
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| Concepts |
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Purinergic signalling
- Receptors
- Pannexins
- Ectonucleotidases
- Metabolism
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| Membrane transporters |
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Nucleoside transporters
- Concentrative
- Equilibrative
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Purinergic receptors, also known as purinoceptors, are a family of plasma membrane molecules that are found in almost all mammalian tissues.[1] Within the field of purinergic signalling, these receptors have been implicated in learning and memory, locomotor and feeding behavior, and sleep.[2] More specifically, they are involved in several cellular functions, including proliferation and migration of neural stem cells, vascular reactivity, apoptosis and cytokine secretion.[3][4] These functions have not been well characterized and the effect of the extracellular microenvironment on their function is also poorly understood.
The term purinergic receptor was originally introduced to illustrate specific classes of membrane receptors that mediate relaxation of gut smooth muscle as a response to the release of ATP (P2 receptors) or adenosine (P1 receptors). P2 receptors have further been divided into five subclasses: P2X, P2Y, P2Z, P2U, and P2T. To distinguish P2 receptors further, the subclasses have been divided into families of metabotropic (P2Y, P2U, and P2T) and ionotropic receptors (P2X and P2Z).[5]
Contents
- 1 3 classes of purinergic receptors
- 2 P2X receptors
- 3 P2Y and P1 receptors
- 4 Inhibitors
- 5 Effects on chronic pain
- 6 Effects on cytotoxic edema
- 7 Effects on diabetes
- 8 See also
- 9 References
- 10 External links
3 classes of purinergic receptors
| Name |
Activation |
Class |
| P1 receptors |
adenosine |
G protein-coupled receptors |
| P2Y receptors |
nucleotides
- ATP
- ADP
- UTP
- UDP
- UDP-glucose
|
G protein-coupled receptors |
| P2X receptors |
ATP |
ligand-gated ion channel |
There are three known distinct classes of purinergic receptors, known as P1, P2X, and P2Y receptors.
P2X receptors
P2X receptors are ligand-gated ion channels, whereas the P1 and P2Y receptors are G protein-coupled receptors. These ligand-gated ion channels are nonselective cation channels responsible for mediating excitatory postsynaptic responses, similar to nicotinic and ionotropic glutamate receptors.[6] P2X receptors are distinct from the rest of the widely known ligand-gated ion channels, as the genetic encoding of these particular channels indicates the presence of only two transmembrane domains within the channels.[7] These receptors are greatly distributed in neurons and glial cells throughout the central and peripheral nervous systems.[8] P2X receptors mediate a large variety of responses including fast transmission at central synapses, contraction of smooth muscle cells, platelet aggregation, macrophage activation, and apoptosis.[9][10] Moreover, these receptors have been implicated in integrating functional activity between neurons, glial, and vascular cells in the central nervous system, thereby mediating the effects of neural activity during development, neurodegeneration, inflammation, and cancer.[11]
P2Y and P1 receptors
Both of these metabotropic receptors are distinguished by their reactivity to specific activators. P1 receptors are preferentially activated by adenosine and P2Y receptors are preferentially more activated by ATP. P1 and P2Y receptors are known to be widely distributed in the brain, heart, kidneys, and adipose tissue. Xanthines (e.g. caffeine) specifically block adenosine receptors, and are known to induce a stimulating effect to one's behavior.[12]
Inhibitors
Inhibitors of purinergic receptors include clopidogrel, prasugrel and ticlopidine, as well as ticagrelor. All of these are antiplatelet agents that block P2Y12 receptors.
Effects on chronic pain
Data obtained from using P2 receptor-selective antagonists has produced evidence supporting ATP's ability to initiate and maintain chronic pain states after exposure to noxious stimuli. It is believed that ATP functions as a pronociceptive neurotransmitter, acting acts at specific P2X and P2Y receptors in a systemized manner, which ultimately (as a response to noxious stimuli) serve to initiate and sustain heightened states of neuronal excitability. This recent knowledge of purinergic receptors' effects on chronic pain provide promise in discovering a drug that specifically targets individual P2 receptor subtypes. While some P2 receptor-selective compounds have proven useful in preclinical trials, more research is required to understand the potential viability of P2 receptor antagonists for pain.[13]
Recent research has identified a role for microglial P2X receptors in neuropathic pain and inflammatory pain, especially the P2X4 and P2X7 receptors.[14][15][16][17][18]
Effects on cytotoxic edema
Purinergic receptors have been suggested to play a role in the treatment of cytotoxic edema and infarctions. It was found that with treatment of the purinergic ligand 2-methylthioladenosine 5' diphosphate (2-MeSADP), which is an agonist and has a high preference for the purinergic receptor type 1 isoform (P2Y1R), significantly contributes to the reduction of a ischemic lesions caused by cytotoxic edema. Further pharmacological evidence has suggested that 2MeSADP protection is controlled by enhanced astrocyte mitochondrial metabolism through increased inositol triphosphate-dependent calcium release. There is evidence suggesting a relationship between the levels of ATP and cytotoxic edema, where low ATP levels are associated with an increased prevalence of cytotoxic edema. It is believed that mitochondria play an essential role in the metabolism of astrocyte energy within the penumbra of ischemic lesions. By enhancing the source of ATP provided by mitochondria, there could be a similar 'protective' effect for brain injuries in general.[19]
Effects on diabetes
Purinergic receptors have been implicated in the vascular complications associated with diabetes due to the effect of high-glucose concentration on ATP-mediated responses in human fibroblasts.[20]
See also
References
- ^ North, R. A. (2002). "Molecular physiology of P2X receptors". Physiological reviews 82 (4): 1013–1067. doi:10.1152/physrev.00015.2002. PMID 12270951. edit
- ^ Burnstock, G. (2013). Introduction to Purinergic Signalling in the Brain. "Glioma Signaling". Advances in experimental medicine and biology. Advances in Experimental Medicine and Biology 986: 1–12. doi:10.1007/978-94-007-4719-7_1. ISBN 978-94-007-4718-0. PMID 22879061. edit
- ^ Ulrich, H.; Abbracchio, M. P.; Burnstock, G. (2012). "Extrinsic Purinergic Regulation of Neural Stem/Progenitor Cells: Implications for CNS Development and Repair". Stem Cell Reviews and Reports 8 (3): 755–767. doi:10.1007/s12015-012-9372-9. PMID 22544361. edit
- ^ Burnstock, G. (2013). Introduction to Purinergic Signalling in the Brain. "Glioma Signaling". Advances in experimental medicine and biology. Advances in Experimental Medicine and Biology 986: 1–12. doi:10.1007/978-94-007-4719-7_1. ISBN 978-94-007-4718-0. PMID 22879061. edit
- ^ King BF, Burnstock G (2002) Purinergic receptors. In: Pangalos M, Davies C (eds) Understanding G protein-coupled receptors and their role in the CNS. Oxford University Press, Oxford, pp 422– 438
- ^ Kaczmarek-Hájek, K.; Lörinczi, É.; Hausmann, R.; Nicke, A. (2012). "Molecular and functional properties of P2X receptors—recent progress and persisting challenges". Purinergic Signalling 8 (3): 375–417. doi:10.1007/s11302-012-9314-7. PMC 3360091. PMID 22547202. edit
- ^ North, R. A. (2002). "Molecular physiology of P2X receptors". Physiological reviews 82 (4): 1013–1067. doi:10.1152/physrev.00015.2002. PMID 12270951. edit
- ^ North, R. A. (2002). "Molecular physiology of P2X receptors". Physiological reviews 82 (4): 1013–1067. doi:10.1152/physrev.00015.2002. PMID 12270951. edit
- ^ Burnstock, G.; Fredholm, B. B.; North, R. A.; Verkhratsky, A. (2010). "The birth and postnatal development of purinergic signalling". Acta Physiologica 199 (2): 93–147. doi:10.1111/j.1748-1716.2010.02114.x. PMID 20345419. edit
- ^ Burnstock, G. (2013). Introduction to Purinergic Signalling in the Brain. "Glioma Signaling". Advances in experimental medicine and biology. Advances in Experimental Medicine and Biology 986: 1–12. doi:10.1007/978-94-007-4719-7_1. ISBN 978-94-007-4718-0. PMID 22879061. edit
- ^ Burnstock, G. (2013). Introduction to Purinergic Signalling in the Brain. "Glioma Signaling". Advances in experimental medicine and biology. Advances in Experimental Medicine and Biology 986: 1–12. doi:10.1007/978-94-007-4719-7_1. ISBN 978-94-007-4718-0. PMID 22879061. edit
- ^ Neuroscience. 2nd edition. Purves D, Augustine GJ, Fitzpatrick D, et al., editors. Sunderland (MA): Sinauer Associates; 2001.
- ^ M.F. Jarvis The neural–glial purinergic receptor ensemble in chronic pain states Trends Neurosci., 33 (2010), pp. 48–57
- ^ Tsuda, M.; Kuboyama, K.; Inoue, T.; Nagata, K.; Tozaki-Saitoh, H.; Inoue, K. (2009). "Behavioral phenotypes of mice lacking purinergic P2X4 receptors in acute and chronic pain assays". Molecular Pain 5: 28. doi:10.1186/1744-8069-5-28. PMC 2704200. PMID 19515262. edit
- ^ Ulmann, L.; Hirbec, H. L. N.; Rassendren, F. O. (2010). "P2X4 receptors mediate PGE2 release by tissue-resident macrophages and initiate inflammatory pain". The EMBO Journal 29 (14): 2290–2300. doi:10.1038/emboj.2010.126. PMC 2910276. PMID 20562826. edit
- ^ Tsuda, M.; Shigemoto-Mogami, Y.; Koizumi, S.; Mizokoshi, A.; Kohsaka, S.; Salter, M. W.; Inoue, K. (2003). "P2X4 receptors induced in spinal microglia gate tactile allodynia after nerve injury". Nature 424 (6950): 778–783. doi:10.1038/nature01786. PMID 12917686. edit
- ^ Kobayashi, K.; Takahashi, E.; Miyagawa, Y.; Yamanaka, H.; Noguchi, K. (2011). "Induction of the P2X7 receptor in spinal microglia in a neuropathic pain model". Neuroscience Letters 504 (1): 57–61. doi:10.1016/j.neulet.2011.08.058. PMID 21924325. edit
- ^ Chessell, I. P.; Hatcher, J. P.; Bountra, C.; Michel, A. D.; Hughes, J. P.; Green, P.; Egerton, J.; Murfin, M.; Richardson, J.; Peck, W. L.; Grahames, C. B. A.; Casula, M. A.; Yiangou, Y.; Birch, R.; Anand, P.; Buell, G. N. (2005). "Disruption of the P2X7 purinoceptor gene abolishes chronic inflammatory and neuropathic pain". Pain 114 (3): 386–396. doi:10.1016/j.pain.2005.01.002. PMID 15777864. edit
- ^ Zheng W, Watts LT, Holstein DM, Prajapati SI, Keller C, et al. (2010) Purinergic Receptor Stimulation Reduces Cytotoxic Edema and Brain Infarcts in Mouse Induced by Photothrombosis by Energizing Glial Mitochondria. PLoS ONE 5(12): e14401. doi:10.1371/journal.pone.00144
- ^ Solini, A.; Chiozzi, P.; Falzoni, S.; Morelli, A.; Fellin, R.; Di Virgilio, F. (2000). "High glucose modulates P2X 7 receptor-mediated function in human primary fibroblasts". Diabetologia 43 (10): 1248–1256. doi:10.1007/s001250051520. PMID 11079743. edit
External links
- IUPHAR GPCR Database - Adenosine receptors
- IUPHAR GPCR Database - P2Y receptors
- Purinergic Receptors at the US National Library of Medicine Medical Subject Headings (MeSH)
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Membrane proteins, receptors: cell surface receptors
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| G protein-coupled receptor |
| Class A |
- Eicosanoid receptor (Prostaglandin receptor)
- Protease-activated receptor
- Neurotransmitter receptor
- Purinergic receptor
- Biogenic amine receptor
- Olfactory receptor
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| Class B |
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| Class C |
- Metabotropic glutamate receptor
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| Class D |
|
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| Class E |
|
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| Class F |
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| Ligand-gated ion channel |
|
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| Enzyme-linked receptor |
- Serine/threonine-specific protein kinase
- Receptor tyrosine kinase
- Guanylate cyclase
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| Other/ungrouped |
- Asialoglycoprotein receptor
- Tumor necrosis factor receptor
- Immunoglobulin superfamily
- N-Acetylglucosamine receptor
- Neuropilins
- Transferrin receptor
- EDAR
- Lipoprotein receptor-related protein
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- See also
- cell surface receptor deficiencies
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)
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Ion channel, cell surface receptor: ligand-gated ion channels
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| Cys-loop receptors |
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5-HT/serotonin
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GABA
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- GABAA
- α1
- α2
- α3
- α4
- α5
- α6
- β1
- β2
- β3
- γ1
- γ2
- γ3
- δ
- ε
- π
- θ
- GABAA-ρ
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Glycine
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Nicotinic acetylcholine
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- monomers: α1
- α2
- α3
- α4
- α5
- α6
- α7
- α9
- α10
- β1
- β2
- β3
- β4
- δ
- ε
- pentamers: (α3)2(β4)3
- (α4)2(β2)3
- (α7)5
- (α1)2(β4)3 - Ganglion type
- (α1)2β1δε - Muscle type
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Zinc
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| Ionotropic glutamates |
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Ligand-gated only
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Voltage- and ligand-gated
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- NMDA
- 1
- 2A
- 2B
- 2C
- 2D
- 3A
- 3B
- L1A
- L1B
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‘Orphan’
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| ATP-gated channels |
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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)
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Cell surface receptor: G protein-coupled receptors
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Class B: Secretin like
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| Orphan |
- GPR (56
- 64
- 97
- 98
- 110
- 111
- 112
- 113
- 114
- 115
- 116
- 123
- 124
- 125
- 126
- 128
- 133
- 143
- 144
- 155
- 157)
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| 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)
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Class C: Metabotropic glutamate / pheromone
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| 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)
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| 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)
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Class F: Frizzled / Smoothened
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| Frizzled |
- Frizzled (1
- 2
- 3
- 4
- 5
- 6
- 7
- 8
- 9
- 10)
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| Smoothened |
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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)
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