Stimulation of the P2Y Purinergic Receptor on Type 1 Astroglia Results in Inositol Phosphate Formation and Calcium Mobilization

Abstract: Cultured astroglia express purinergic receptors that initiate phosphoinositide metabolism and calcium mobilization. Experiments were conducted to characterize the purinergic receptor subtype on type 1 astroglia responsible for stimulating these second‐messenger systems. Inositol phosphate (IP) accumulation and calcium mobilization were measured after stimulation with ATP or purinergic receptor subtype‐selective ATP analogues. ATP (10–5M) increased IP accumulation severalfold. Dose–effect assays monitoring astroglial IP accumulation revealed the order of potency that defines the P2Y receptor: 2‐methylthioadenosine 5′‐triphosphate > ATP > αβ‐methyleneadenosine 5′‐triphosphate > βγ‐methyleneadenosine 5′‐triphosphate. The influence of ATP on intracellular calcium levels in individual type 1 astroglia was examined using the calcium indicator dye, fura‐2. Dose–effect experiments indicated that ATP was equally potent for generating inositol phosphates and increasing cellular calcium. The most prevalent response (87% of total responses) to ATP consisted of a rapid increase in calcium to a peak level that was approximately five times greater than the prestimulation level. This peak was followed by a decline to a plateau level that was significantly above baseline. This plateau phase of the calcium increase was maintained for at least 5 min in the presence of ATP and was dependent on external calcium. Many (23%) astroglia exhibited spontaneous calcium oscillations whose frequency and magnitude increased after the addition of 10–5M ATP. Immunocytochemical staining indicated that the responses occurred in glial fibrillary acidic protein positive cells. We conclude that type 1 astroglia express the P2Y purinergic receptor which regulates IP production and calcium mobilization.

[1]  T. Stone Cell-membrane receptors for purines , 1982, Bioscience reports.

[2]  G. Burnstock Overview: Purinergic Mechanisms , 1990, Annals of the New York Academy of Sciences.

[3]  S. Murphy,et al.  Receptor-mediated inositol phospholipid hydrolysis in astrocytes. , 1986, European journal of pharmacology.

[4]  P. Dandona,et al.  Astrocytes as eicosanoid‐producing cells , 1988, Glia.

[5]  P. Blackmore,et al.  Characterization of responses of isolated rat hepatocytes to ATP and ADP. , 1985, The Journal of biological chemistry.

[6]  G Burnstock,et al.  Is there a basis for distinguishing two types of P2-purinoceptor? , 1985, General pharmacology.

[7]  L. Heppel,et al.  Control of membrane permeability by external and internal ATP in 3T6 cells grown in serum-free medium. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[8]  K. McCarthy,et al.  Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue , 1980, The Journal of cell biology.

[9]  M. Norenberg,et al.  ATP stimulates calcium influx in primary astrocyte cultures. , 1988, Biochemical and biophysical research communications.

[10]  T. Rink,et al.  Calcium oscillations in non-excitable cells , 1989, Trends in Neurosciences.

[11]  K. McCarthy,et al.  Immunocytochemically defined astroglia from fetal, newborn and young adult rats express beta-adrenergic receptors in vitro. , 1986, Brain research.

[12]  J. García-Sancho,et al.  Mobilization of intracellular calcium by extracellular ATP and by calcium ionophores in the Ehrlich ascites-tumour cell. , 1988, Biochimica et biophysica acta.

[13]  L. Eng,et al.  Localization of the glial fibrillary acidic protein in astrocytes by immunofluorescence. , 1972, Brain research.

[14]  J. Häggblad,et al.  Externally applied adenosine-5′-triphosphate causes inositol triphosphate accumulation in cultured chick myotubes , 1987, Neuroscience Letters.

[15]  J. Boeynaems,et al.  Stimulation of vascular prostacyclin synthesis by extracellular ADP and ATP. , 1983, Biochemical and biophysical research communications.

[16]  S. Finkbeiner,et al.  Glutamate induces calcium waves in cultured astrocytes: long-range glial signaling. , 1990, Science.

[17]  G. Dubyak Extracellular ATP activates polyphosphoinositide breakdown and Ca2+ mobilization in Ehrlich ascites tumor cells. , 1986, Archives of biochemistry and biophysics.

[18]  M. Berridge,et al.  Cytosolic calcium oscillators , 1988, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[19]  Michael J. Berridge,et al.  Inositol phosphates and cell signalling , 1989, Nature.

[20]  Michael J. Berridge,et al.  Inositol trisphosphate, a novel second messenger in cellular signal transduction , 1984, Nature.

[21]  E. Trams Evidence for ATP action on the cell surface , 1974, Nature.

[22]  M. Berridge,et al.  Changes in the levels of inositol phosphates after agonist-dependent hydrolysis of membrane phosphoinositides. , 1983, The Biochemical journal.

[23]  S. Murphy,et al.  ATP‐Evoked Ca2+ Mobilisation and Prostanoid Release from Astrocytes: P2‐Purinergic Receptors Linked to Phosphoinositide Hydrolysis , 1989, Journal of neurochemistry.

[24]  G. Burnstock,et al.  ATP mediates coronary vasoconstriction via P2x-purinoceptors and coronary vasodilatation via P2y-purinoceptors in the isolated perfused rat heart. , 1987, European journal of pharmacology.

[25]  J. Pearson,et al.  Exogenous ATP raises cytoplasmic free calcium in fura‐2 loaded piglet aortic endothelial cells , 1986, FEBS letters.

[26]  J. Young,et al.  Extracellular ATP perturbs transmembrane ion fluxes, elevates cytosolic [Ca2+], and inhibits phagocytosis in mouse macrophages. , 1985, The Journal of biological chemistry.

[27]  K. McCarthy,et al.  Norepinephrine‐evoked calcium transients in cultured cerebral type 1 astroglia , 1990, Glia.

[28]  K. McCarthy,et al.  Pharmacologically-distinct subsets of astroglia can be identified by their calcium response to neuroligands , 1991, Neuroscience.

[29]  M. Thorner,et al.  Spontaneous oscillations of intracellular calcium and growth hormone secretion. , 1988, The Journal of biological chemistry.

[30]  T. K. Harden,et al.  Kinetics of activation of phospholipase C by P2Y purinergic receptor agonists and guanine nucleotides. , 1989, The Journal of biological chemistry.

[31]  C. D. Benham,et al.  A novel receptor-operated Ca2+-permeable channel activated by ATP in smooth muscle , 1987, Nature.

[32]  G. Feuerstein,et al.  Adenosine triphosphate stimulates inositol phospholipid metabolism and prostacyclin formation in adrenal medullary endothelial cells by means of P2-purinergic receptors. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[33]  J. Putney Capacitative calcium entry revisited. , 1990, Cell calcium.

[34]  S. Murphy,et al.  Eicosanoids in the CNS: sources and effects. , 1988, Prostaglandins, leukotrienes, and essential fatty acids.

[35]  J. Pearson,et al.  Regulation of P2y‐purinoceptor‐mediated prostacyclin release from human endothelial cells by cytoplasmic calcium concentration , 1988, British journal of pharmacology.

[36]  J. L. Gordon Extracellular ATP: effects, sources and fate. , 1986, The Biochemical journal.

[37]  G. Burnstock Dual Control of Local Blood Flow by Purines a , 1990, Annals of the New York Academy of Sciences.

[38]  S. Hourani,et al.  Characterisation of ADP receptors. , 1985, Advances in experimental medicine and biology.

[39]  W. Martin,et al.  Specificity of P2-purinoceptor that mediates endothelium-dependent relaxation of the pig aorta. , 1985, European journal of pharmacology.

[40]  S. Murphy,et al.  ATP‐Evoked Arachidonic Acid Mobilization in Astrocytes Is via a P2Y‐Purinergic Receptor , 1990, Journal of neurochemistry.

[41]  Y. Tokumitsu,et al.  P2-purinergic receptors are coupled to two signal transduction systems leading to inhibition of cAMP generation and to production of inositol trisphosphate in rat hepatocytes. , 1987, The Journal of biological chemistry.

[42]  P. Mobley,et al.  Protein Phosphorylation in Astrocytes Mediated by Protein Kinase C: Comparison with Phosphorylation by Cyclic AMP‐Dependent Protein Kinase , 1989, Journal of neurochemistry.