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[en] Short communication
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[en] Regulation of the sodium permeability of the luminal membrane is the major mechanism by which the net rate of sodium transport across tight epithelia is varied. Previous evidence has suggested that the permeability of the luminal membrane might be regulated by changes in intracellular sodium or calcium activities. To test this directly, we isolated a fraction of the plasma membrane from the toad urinary bladder, which contains a fast, amiloride-sensitive sodium flux with characteristics similar to those of the native luminal membrane. Using a flow-quench apparatus to measure the initial rate of sodium efflux from these vesicles in the millisecond time range, we have demonstrated that the isotope exchange permeability of these vesicles is very sensitive to calcium. Calcium reduces the sodium permeability, and the half-maximal inhibitory concentration is 0.5 microM, well within the range of calcium activity found in cells. Also, the permeability of the luminal membrane vesicles is little affected by the ambient sodium concentration. These results, when taken together with studies on whole tissue, suggest that cell calcium may be an important regulator of transepithelial sodium transport by its effect on luminal sodium permeability. The effect of cell sodium on permeability may be mediated by calcium rather than by sodium itself
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Journal of General Physiology; ISSN 0022-1295; ; v. 81(5); p. 643-665
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[en] Chloride channels mediate absorption and secretion of fluid in epithelia, and the regulation of these channels is now known to be defective in cystic fibrosis. Indanyl-oxyacetic acid 94 (IAA-94) is a high-affinity ligand for the chloride channel, and an affinity resin based on that structure was developed. Solubilized proteins from kidney and trachea membranes were applied to the affinity matrix, and four proteins with apparent molecular masses of 97, 64, 40, and 27 kilodaltons were eluted from the column by excess IAA-94. A potential-dependent 36Cl- uptake was observed after reconstituting these proteins into liposomes. Three types of chloride channels with single-channel conductances of 26, 100, and 400 picosiemens were observed after fusion of these liposomes with planar lipid bilayers. Similar types of chloride channels have been observed in epithelia
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ANIMALS, ANTIBIOTICS, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, BETA-PLUS DECAY RADIOISOTOPES, BODY, CELL CONSTITUENTS, CHLORINE COMPOUNDS, CHLORINE ISOTOPES, DISEASES, DOMESTIC ANIMALS, DRUGS, ELECTRON CAPTURE RADIOISOTOPES, HALIDES, HALOGEN COMPOUNDS, ISOTOPE APPLICATIONS, ISOTOPES, LIGHT NUCLEI, MAMMALS, MEMBRANES, NUCLEI, ODD-ODD NUCLEI, ORGANIC COMPOUNDS, ORGANS, PIGMENTS, RADIOISOTOPES, RESPIRATORY SYSTEM, RUMINANTS, SEPARATION PROCESSES, TISSUES, VERTEBRATES, YEARS LIVING RADIOISOTOPES
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