Zobrazeno 1 - 10
of 15
pro vyhledávání: '"E. R. Lazarowski"'
Publikováno v:
British journal of pharmacology. 153(7)
The P2Y14 receptor is activated by UDP-sugars, most potently by UDP-glucose, but not by free nucleotides, suggesting that UDP-glucose is the cognate agonist for this receptor. However, evidence for regulated release of UDP-glucose is scarce. In the p
Publikováno v:
Journal of Biological Chemistry. 265:13118-13123
Human erythroleukemia (HEL) cells phosphorylate [3H]inositol 1,4,5-trisphosphate to inositol 1,3,4,5-tetrakisphosphate; they also contain all the enzymes to sequentially dephosphorylate [3H]inositol 1,4,5-trisphosphate and [3H]inositol 1,3,4,5-tetrak
Autor:
E R, Lazarowski, L G, Rochelle, W K, O'Neal, C M, Ribeiro, B R, Grubb, V, Zhang, T K, Harden, R C, Boucher
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 297(1)
Extracellular nucleotides regulate transepithelial ion secretion via multiple receptors. The P2Y(2) receptor is the predominant transducer of chloride transport responses to nucleotides in the airways, but the P2 receptors that control ion transport
Publikováno v:
Molecular medicine (Cambridge, Mass.). 6(11)
BACKGROUND: Cystic fibrosis (CF) is a syndrome caused by mutations in the cystic fibrosis transmembrane regulator (CFTR) gene. Despite advances in our understanding of the molecular pathogenesis of CF, the link between CFTR gene mutations and the pat
Publikováno v:
Arthritis and rheumatism. 43(7)
To determine whether ATP is released from chondrocytes during mechanical stimulation and whether degradation of ATP generates inorganic pyrophosphate in chondron pellet cultures.Chondron pellets were formed from 1.6 x 10(6) cells that had been enzyma
Autor:
T K, Harden, E R, Lazarowski
Publikováno v:
Progress in brain research. 120
Publikováno v:
The Journal of biological chemistry. 273(22)
The cystic fibrosis (CF) transmembrane regulator (CFTR) is a cyclic AMP-dependent Cl- channel that is defective in CF cells. It has been hypothesized that CFTR exhibits an ATP release function that controls the airway surface ATP concentrations. In a
Publikováno v:
Trends in pharmacological sciences. 18(2)
Publikováno v:
Molecular pharmacology. 50(2)
Observation that the G protein-coupled P2U receptor (P2Y2 receptor) is activated by UTP as well as ATP provided the first indication that a class of uridine nucleotide-responsive receptors might exist. This hypothesis was confirmed by our identificat
Autor:
E R, Lazarowski, T K, Harden
Publikováno v:
The Journal of biological chemistry. 269(16)
Incubation of C6-2B rat glioma cells with UDP or UTP resulted in a time- and concentration-dependent increase in the accumulation of inositol phosphates. In contrast, ATP, ADP, and analogs of these nucleotides known to be effective agonists at P2U-,