The efficacy of muscarinic-receptor agonists for stimulation of inositol phosphate formation and Ca2+ mobilization in intact 1321N1 human astrocytoma cells is correlated with their capacity for formation of a GTP-sensitive high-affinity binding complex in membranes from these cells [Evans, Hepler, Masters, Brown & Harden (1985) Biochem. J. 232, 751-757]. These observations prompted the proposal that a guanine nucleotide regulatory protein serves to couple muscarinic receptors to the phospholipase C involved in phosphoinositide hydrolysis in 1321N1 cells. Inositol phosphate (InsP) formation was measured in a cell-free preparation from 1321N1 cells to provide direct support for this idea. The formation of InsP3, InsP2 and InsP1 was increased ...
AbstractRecent evidence has suggested that receptor-mediated phosphoinositide turnover, like that of...
AbstractMembranes isolated from Acer pseudoplatanus cell suspension cultures that were prelabelled w...
It has been proposed elsewhere [Meeker, R. B. & Harden, T. K. (1982) Mol. Pharmacol. 22, 310-319] th...
The efficacy of muscarinic-receptor agonists for stimulation of inositol phosphate formation and Ca2...
AbstractHydrolysis-resistant analogues of GTP specifically stimulate the formation of [3H]inositol m...
The relative capacities of muscarinic cholinergic receptor (MR) and bradykinin (BK)-receptor activat...
The efficacies of a series of six muscarinic cholinergic receptor agonists for stimulation of phosph...
Although activation of muscarinic cholinergic receptors on 1321N1 human astrocytoma cells results in...
Incubation of C6-2B rat glioma cells with UDP or UTP resulted in a time- and concentration-dependent...
AbstractPretreatment of human embryonic pituitary tumour cells (Flow 9000) with pertussis toxin sign...
Inhibitory coupling of receptors to adenylate cyclase previously has been shown to be relatively sen...
Pertussis toxin was used to examine the role of the inhibitory guanine nucleotide regulatory protein...
AbstractPrevious studies have shown that agonist-induced inositol phosphate formation in the human e...
The possibility that an increased intracellular concentration of cyclic AMP (cAMP) can regulate the ...
AbstractMastoparan inhibited [3H]inositol phosphate accumulation induced by carbachol as well as cyc...
AbstractRecent evidence has suggested that receptor-mediated phosphoinositide turnover, like that of...
AbstractMembranes isolated from Acer pseudoplatanus cell suspension cultures that were prelabelled w...
It has been proposed elsewhere [Meeker, R. B. & Harden, T. K. (1982) Mol. Pharmacol. 22, 310-319] th...
The efficacy of muscarinic-receptor agonists for stimulation of inositol phosphate formation and Ca2...
AbstractHydrolysis-resistant analogues of GTP specifically stimulate the formation of [3H]inositol m...
The relative capacities of muscarinic cholinergic receptor (MR) and bradykinin (BK)-receptor activat...
The efficacies of a series of six muscarinic cholinergic receptor agonists for stimulation of phosph...
Although activation of muscarinic cholinergic receptors on 1321N1 human astrocytoma cells results in...
Incubation of C6-2B rat glioma cells with UDP or UTP resulted in a time- and concentration-dependent...
AbstractPretreatment of human embryonic pituitary tumour cells (Flow 9000) with pertussis toxin sign...
Inhibitory coupling of receptors to adenylate cyclase previously has been shown to be relatively sen...
Pertussis toxin was used to examine the role of the inhibitory guanine nucleotide regulatory protein...
AbstractPrevious studies have shown that agonist-induced inositol phosphate formation in the human e...
The possibility that an increased intracellular concentration of cyclic AMP (cAMP) can regulate the ...
AbstractMastoparan inhibited [3H]inositol phosphate accumulation induced by carbachol as well as cyc...
AbstractRecent evidence has suggested that receptor-mediated phosphoinositide turnover, like that of...
AbstractMembranes isolated from Acer pseudoplatanus cell suspension cultures that were prelabelled w...
It has been proposed elsewhere [Meeker, R. B. & Harden, T. K. (1982) Mol. Pharmacol. 22, 310-319] th...