Abstract
Cell membranes isolated from hamster insulinoma (HIT T15) cells at passages 65-74 contain high and low affinity receptors for a sulfonylurea derivative, 5-[125I]iodo,2-hydroxyglyburide (KD values of approximately 7 nM and 16 microM). Between passages 75 and 85, the estimated B(max) for the high affinity receptor decreases approximately 10-fold from approximately 1.6 to 0.16 pmol/mg membrane protein. By contrast, the density of low affinity binding sites, 800-1000 pmol/mg, is unaltered. The drop in high affinity receptors is paralleled by a decrease in the density of KATP channels assessed using patch-clamp and 86Rb(+)-efflux techniques. These results strongly support the idea that the high affinity sulfonylurea receptor is an integral part of the KATP channel.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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ATP-Binding Cassette Transporters*
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Adenosine Triphosphate / metabolism*
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Affinity Labels
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Animals
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Autoradiography
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Biological Transport
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Cricetinae
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Electrophoresis, Polyacrylamide Gel
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Glyburide / analogs & derivatives
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Glyburide / metabolism
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Insulinoma / metabolism*
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Iodine Radioisotopes
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Potassium Channels / metabolism*
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Potassium Channels, Inwardly Rectifying*
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Receptors, Drug / metabolism*
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Rubidium / metabolism
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Sulfonylurea Receptors
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Tumor Cells, Cultured
Substances
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ATP-Binding Cassette Transporters
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Affinity Labels
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Iodine Radioisotopes
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Potassium Channels
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Potassium Channels, Inwardly Rectifying
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Receptors, Drug
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Sulfonylurea Receptors
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5-iodo-2-hydroxyglyburide
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Adenosine Triphosphate
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Rubidium
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Glyburide