Second-messenger responses associated with stimulation of neuronal muscarinic receptors expressed by a human neuroblastoma SH-SY5Y.
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[1] R. Wojcikiewicz,et al. Phosphoinositide hydrolysis in permeabilized SH‐SY5Y human neuroblastoma cells is inhibited by mastoparan , 1989, FEBS letters.
[2] S. Nahorski. Inositol polyphosphates and neuronal calcium homeostasis , 1988, Trends in Neurosciences.
[3] Y. Nozawa,et al. Bradykinin-induced generation of inositol 1,4,5-trisphosphate in fibroblasts and neuroblastoma cells: effect of pertussis toxin, extracellular calcium, and down-regulation of protein kinase C. , 1988, Biochemical and biophysical research communications.
[4] S. Nahorski,et al. Muscarinic receptor binding characteristics of a human neuroblastoma SK-N-SH and its clones SH-SY5Y and SH-EP1. , 1989, European journal of pharmacology.
[5] J. Meldolesi,et al. The intracellular distribution of calcium , 1988, Trends in Neurosciences.
[6] K. Krause,et al. "Calciosome," a cytoplasmic organelle: the inositol 1,4,5-trisphosphate-sensitive Ca2+ store of nonmuscle cells? , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[7] S. Fisher,et al. A Putative M3 Muscarinic Cholinergic Receptor of High Molecular Weight Couples to Phosphoinositide Hydrolysis in Human SK‐N‐SH Neuroblastoma Cells , 1988, Journal of neurochemistry.
[8] S. Lazareno,et al. Pirenzepine indicates heterogeneity of muscarinic receptors linked to cerebral inositol phospholipid metabolism , 1985, Neuropharmacology.
[9] D. Lambert,et al. Muscarinic receptors coupled to phosphoinositide hydrolysis and elevated cytosolic calcium in a human neuroblastoma cell line SK‐N‐SH , 1989, British journal of pharmacology.
[10] V. Gallo,et al. Selective release of glutamate from cerebellar granule cells differentiating in culture. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[11] D. Kendall,et al. Receptors and phosphoinositide metabolism in the central nervous system. , 1986, Biochemical pharmacology.
[12] S. Fisher,et al. Recognition of muscarinic cholinergic receptors in human SK-N-SH neuroblastoma cells by quaternary and tertiary ligands is dependent upon temperature, cell integrity, and the presence of agonists. , 1988, Molecular pharmacology.
[13] I. Batty,et al. Mass measurements of inositol(1,4,5)trisphosphate in rat cerebral cortex slices using a radioreceptor assay: effects of neurotransmitters and depolarization. , 1988, Biochemical and biophysical research communications.
[14] T. Rink,et al. Agonists stimulate divalent cation channels in the plasma membrane of human platelets , 1985, FEBS letters.
[15] M. Berridge,et al. Cytosolic calcium oscillators , 1988, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[16] J. Christophe,et al. 80% of muscarinic receptors expressed by the NB‐OK 1 human neuroblastoma cell line show high affinity for pirenzepine and are comparable to rat hippocampus M1 receptors , 1988, FEBS letters.
[17] E. Sher,et al. Pharmacological Characterization of Cholinergic Receptors in a Human Neuroblastoma Cell Line , 1986, Journal of neurochemistry.
[18] R. Snider,et al. Differential receptor occupancy requirements for muscarinic cholinergic stimulation of inositol lipid hydrolysis in brain and in neuroblastomas. , 1987, Molecular pharmacology.
[19] North Ra,et al. Control of ion conductances by muscarinic receptors. , 1988 .
[20] P. Fishman,et al. Muscarinic receptor-mediated increase in cAMP levels in SK-N-SH human neuroblastoma cells. , 1988, Biochemical and biophysical research communications.
[21] H. Yamamura,et al. Muscarinic receptor-mediated hydrolysis of phosphatidylinositols in human neuroblastoma (SH-SY5Y) cells is sensitive to pertussis toxin , 1988, Brain Research.
[22] J. Baumgold,et al. Pharmacological differences between muscarinic receptors coupled to phosphoinositide turnover and those coupled to adenylate cyclase inhibition. , 1989, Biochemical pharmacology.
[23] B. Potter,et al. Molecular recognition of inositol polyphosphates by intracellular receptors and metabolic enzymes. , 1989, Trends in pharmacological sciences.
[24] J. Meldolesi,et al. Generation of inositol phosphates, cytosolic Ca2+, and ionic fluxes in PC12 cells treated with bradykinin. , 1988, The Journal of biological chemistry.
[25] A. Ashkenazi,et al. Differential regulation of PI hydrolysis and adenylyl cyclase by muscarinic receptor subtypes , 1988, Nature.
[26] K. McCarthy,et al. Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue , 1980, The Journal of cell biology.
[27] T. Bonner,et al. Antagonist binding properties of five cloned muscarinic receptors expressed in CHO-K1 cells. , 1989, Molecular pharmacology.
[28] C. D. Benham,et al. A novel receptor-operated Ca2+-permeable channel activated by ATP in smooth muscle , 1987, Nature.
[29] P. Barnes,et al. Mass changes of inositol(1,4,5)trisphosphate in trachealis muscle following agonist stimulation. , 1989, European journal of pharmacology.
[30] P. Gray. Oscillations of free cytosolic calcium evoked by cholinergic and catecholaminergic agonists in rat parotid acinar cells. , 1988, The Journal of physiology.
[31] A. Nordberg,et al. Muscarinic receptors in human SH-SY5Y neuroblastoma cell line: regulation by phorbol ester and retinoic acid-induced differentiation. , 1987, Brain research.
[32] T. Bonner,et al. Identification of a family of muscarinic acetylcholine receptor genes. , 1987, Science.
[33] T. Bonner,et al. Cloning and expression of the human and rat m5 muscarinic acetylcholine receptor genes , 1988, Neuron.
[34] S. Fisher,et al. Muscarinic receptor regulation of cytoplasmic Ca2+ concentrations in human SK-N-SH neuroblastoma cells: Ca2+ requirements for phospholipase C activation. , 1989, Molecular pharmacology.
[35] T. Hallam,et al. Platelets and parotid acinar cells have different mechanisms for agonist-stimulated divalent cation entry. , 1988, The Journal of biological chemistry.
[36] J. Meldolesi,et al. Second-messenger generation in PC12 cells. Interactions between cyclic AMP and Ca2+ signals. , 1988, The Biochemical journal.
[37] W. Schlegel,et al. Lowering of cytosolic free Ca2+ by carbachol, a muscarinic cholinergic agonist, in clonal pituitary cells (GH3 cells). , 1985, Endocrinology.
[38] J. Putney,et al. Capacitative calcium entry in parotid acinar cells. , 1989, The Biochemical journal.
[39] K. Åkerman,et al. Depolarization of human neuroblastoma cells as a result of muscarinic receptor‐induced rise in cytosolic Ca2+ , 1989, FEBS letters.
[40] N. Birdsall,et al. Muscarinic receptor subtypes. , 1990, Annual review of pharmacology and toxicology.
[41] R. Tsien,et al. A new generation of Ca2+ indicators with greatly improved fluorescence properties. , 1985, The Journal of biological chemistry.
[42] J. Meldolesi,et al. Pathways of Ca2+ influx at the plasma membrane: voltage-, receptor-, and second messenger-operated channels. , 1987, Experimental cell research.
[43] R. Ross,et al. Presence and regulation of tyrosinase activity in human neuroblastoma cell variants in vitro. , 1985, Cancer research.
[44] E. Barnard. Separating receptor subtypes from their shadows , 1988, Nature.
[45] I. G. Scott,et al. Development of a neural phenotype in differentiating ganglion cell‐derived human neuroblastoma cells , 1986, Journal of cellular physiology.
[46] I. Batty,et al. Accumulation of inositol polyphosphate isomers in agonist-stimulated cerebral-cortex slices. Comparison with metabolic profiles in cell-free preparations. , 1989, The Biochemical journal.
[47] S. Muallem,et al. The agonist-sensitive calcium pool in the pancreatic acinar cell. Activation of plasma membrane Ca2+ influx mechanism. , 1987, The Journal of biological chemistry.
[48] M. J. Berridge,et al. Release of Ca2+ from a nonmitochondrial intracellular store in pancreatic acinar cells by inositol-1,4,5-trisphosphate , 1983, Nature.
[49] P. Negulescu,et al. Release and reloading of intracellular Ca stores after cholinergic stimulation of the parietal cell. , 1988, The American journal of physiology.
[50] I. G. Scott,et al. Differentiation‐associated decrease in muscarinic receptor sensitivity in human neuroblastoma cells , 1987, Journal of cellular physiology.
[51] M. Berridge,et al. Inositol trisphosphate and diacylglycerol: two interacting second messengers. , 1987, Annual review of biochemistry.
[52] F M Matschinsky,et al. Cell-specific patterns of oscillating free Ca2+ in carbamylcholine-stimulated insulinoma cells. , 1988, The Journal of biological chemistry.
[53] T. Rink,et al. Regulation of cytosolic free calcium in fura-2-loaded rat parotid acinar cells. , 1987, The Journal of biological chemistry.
[54] S. Muallem,et al. Two components of hormone-evoked calcium release from intracellular stores of pancreatic acinar cells. , 1988, The Biochemical journal.
[55] M. Mishina,et al. Selective coupling with K+ currents of muscarinic acetylcholine receptor subtypes in NG108-15 cells , 1988, Nature.
[56] P. Cobbold,et al. Fluorescence and bioluminescence measurement of cytoplasmic free calcium. , 1987, The Biochemical journal.
[57] S. Nahorski,et al. Muscarinic-receptor-mediated changes in intracellular Ca2+ and inositol 1,4,5-trisphosphate mass in a human neuroblastoma cell line, SH-SY5Y. , 1990, The Biochemical journal.
[58] J. Eubanks,et al. Desensitization and recovery of muscarinic and histaminergic Ca2+ mobilization in 1321N1 astrocytoma cells. , 1988, The Biochemical journal.
[59] D. Kendall,et al. Inositol Phospholipid Hydrolysis in Rat Cerebral Cortical Slices: I. Receptor Characterisation , 1984, Journal of neurochemistry.
[60] B. Spengler,et al. Morphology and growth, tumorigenicity, and cytogenetics of human neuroblastoma cells in continuous culture. , 1973, Cancer research.
[61] M. Blaustein. Calcium transport and buffering in neurons , 1988, Trends in Neurosciences.
[62] H. Yamamura,et al. The Intact Human Neuroblastoma Cell (SH‐SY5Y) Exhibits High‐Affinity [3H]Pirenzepine Binding Associated with Hydrolysis of Phosphatidylinositols , 1988, Journal of neurochemistry.
[63] W. Sadee,et al. Differential expression of α‐subunits of G‐proteins in human neuroblastoma‐derived cell clones , 1987 .