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Nucleotide‐evoked calcium signals and anion secretion in equine cultured epithelia that express apical P2Y 2 receptors and pyrimidine nucleotide receptors
Author(s) -
Wilson S M,
Law V W Y,
Pediani J D,
Allen E A,
Wilson G,
Khan Z E,
Ko W H
Publication year - 1998
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0701888
Subject(s) - p2y receptor , receptor , nucleotide , suramin , bapta , purinergic receptor , intracellular , population , calcium , biology , chemistry , biochemistry , microbiology and biotechnology , medicine , environmental health , organic chemistry , gene
Experiments with a spontaneously transformed equine epithelial cell line showed that certain nucleotides increased intracellular free calcium ([Ca 2+ ] i ) in cells plated on glass coverslips. The rank order of potency was ATP=UTP>5‐Br‐UTP, whilst UDP and ADP were ineffective. The response thus appears to be mediated by P2Y 2 receptors. Nucleotides also increased short circuit current ( I SC ) in cells grown into epithelial monolayers and the rank order of potency was UDP>UTP>5‐Br‐UTP>ATP>ADP. The increase in [Ca 2+ ] i and the rise in I SC thus have different pharmacological properties. Cross‐desensitization experiments indicated that, as well as P2Y 2 receptors, the monolayer cultures express at least one additional receptor population that allowed nucleotides to increase I SC . The UDP‐evoked increase in I SC was essentially abolished in BAPTA‐loaded epithelia suggesting that this response is dependent upon increased [Ca 2+ ] i . Moreover, experiments in which I SC and [Ca 2+ ] i were measured simultaneously showed that the UDP‐ and ADP‐evoked increases in I SC were accompanied by increases in [Ca 2+ ] i . When grown under conditions which favour the development of a polarized phenotype, these epithelial cells thus appear to express [Ca 2+ ] i ‐mobilizing receptors sensitive to UDP and ADP that are not present in non‐polarized cells on coverslips.
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