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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1991-1-29
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pubmed:abstractText |
1. Using the perforated patch recording, the effects of ATP on membrane current were investigated in mouse peritoneal macrophages. 2. Extracellularly applied ATP induced a biphasic current consisting of a initial inward current [Ii(ATP)] followed by an outward current [Io(ATP)]. These currents were associated with a marked increase in conductance at their peaks. 3. Ii(ATP) reversed close to 0 mV and was attenuated by removal of external Na+. 4. Io(ATP) reversed near -80 mV and was increased by decreasing the external concentration of K+. 5. Io(ATP) was completely abolished by removal of external Ca2+, treatment with an intracellular Ca2+ chelator, the acetoxymethyl ester of 1,2-bis (2-aminophenoxy) ethane-N,N,N',N'-tetra acetic acid (BAPTA-AM) and bath applied quinidine but not tetraethylammonium (TEA) or apamin. 6. These results suggest that Ii(ATP) and Io(ATP) are due to an activation of nonspecific cationic and Ca2(+)-dependent K+ conductances, respectively, and raise the possibility that the putative ATP receptor may be important in regulating macrophage functions, motility, phagocytosis and cytokines secretion.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0300-9629
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
97
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
417-21
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pubmed:dateRevised |
2008-10-30
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pubmed:meshHeading |
pubmed-meshheading:1979534-Adenosine Triphosphate,
pubmed-meshheading:1979534-Animals,
pubmed-meshheading:1979534-Calcium,
pubmed-meshheading:1979534-Cells, Cultured,
pubmed-meshheading:1979534-Electric Conductivity,
pubmed-meshheading:1979534-Macrophages,
pubmed-meshheading:1979534-Membrane Potentials,
pubmed-meshheading:1979534-Mice,
pubmed-meshheading:1979534-Potassium,
pubmed-meshheading:1979534-Potassium Channels
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pubmed:year |
1990
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pubmed:articleTitle |
Extracellular ATP activates Ca2(+)-dependent K+ conductance via Ca2+ influx in mouse macrophages.
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pubmed:affiliation |
Central Research Laboratories, Shimane Medical University, Izumo, Japan.
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pubmed:publicationType |
Journal Article
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