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  • Ciliary epithelium  (2)
  • Na+/H+ antiport  (2)
  • 1
    ISSN: 1432-2013
    Keywords: Ciliary epithelium ; Tissue culture ; Na+/H+ exchange ; Amiloride
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Uptake studies with22Na were performed in cultured bovine pigmented ciliary epithelial cells, in order to characterize mechanisms of Na+ transport. A large part of Na+ uptake was sensitive to amiloride, quinidine and harmaline. Na+ uptake was stimulated by intracellular acidification (using the NH 4 + prepulse technique), and was inhibited with increasing extracellular proton concentration. Decreasing extracellular pH from 7.5 to 7.0 increased the apparentK M for Na+ from 38 to 86 mM without considerable changes inV max. In the presence of 5 mM Na+ half maximal inhibition of amiloride sensitive Na+ uptake by extracellular protons was observed at a hydrogen concentration of 50 nM. In the presence of 50 mM Na+ the proton concentration necessary for 50% inhibition was 139 nM. Thus, the mode of inhibition of extracellular H+ seemed to be competitive with aK i of 20–40 nM. 10 μM amiloride increased the apparentK M for Na+ from 33 mM to 107 mM, whileV max remained nearly unchanged. IC50 for amiloride was 6 μM at 5 mM Na+ and 36 μM in the presence of 150 mM Na+. Thus, amiloride behaves as a competitive inhibitor with aK i of about 5 μM. The affinities of Na+ to the transport site (K M≈16 mM), to the inhibitory site for protons (K M≈21 mM), and to the inhibitory site for amiloride (K M≈26 mM) were in the same order of magnitude. In summary, we have presented evidence for the presence of a Na+/H+ exchanger in cultured bovine pigmented ciliary epithelial cells. The kinetic data suggest the presence of only one common extracellular binding site for Na+, H+ and amiloride.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 407 (1986), S. S112 
    ISSN: 1432-2013
    Keywords: Ciliary epithelium ; Shark ; Intracellular membrane potential ; Intracellular chloride activity ; Ouabain ; Furosemide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We have found that membrane potential in the isolated ciliary epithelium of the shark,Squalus acanthias, is −53 mV. High extracellular potassium or ouabain (10−5 mol·l−1) decrease the potential, and furosemide (10−4 mol·l−1) hyperpolarizes it. There is no difference in membrane potential between the cells of the non-pigmented and pigmented layers. Intracellular chloride activity (64 mmol·l−1) was significantly higher than could be predicted from the equilibrium distribution (26 mmol·l−1) across the cell membranes. When furosemide was applied to the aqueous side of the epithelium, intracellular chloride activity decreased to 35 mmol·l−1 and approached electrochemical equilibrium. The data indicate that the ciliary epithelium possesses an active, furosemide-sensitive chloride transport mechanism which could be a Na−Cl or a 1 Na-1 K-2 Cl symport.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2013
    Keywords: Cell culture ; pH sensitive dyes ; pH sensitive absorbance ; 5 (and 6)-carboxy-dimethylfluorescein ; Na+/H+ antiport ; Cl−/HCO 3 − exchange
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Regulation of intracellular pH (pHi) in bovine retinal pigment epithelium (RPE) was investigated in cell culture. pHi was measured using the pH-sensitive absorbance of intracellularly trapped 5 (and 6)-carboxy-dimethyl-fluorescein (CDMF). (1) Regulation of pHi after induction of an acid load by removal of NH4Cl could be blocked either totally by removal of extracellular sodium, or subtotally (about 90%) by application of amiloride (1 mmol/l). Additional flux measurements revealed a dose-dependent, amiloride-sensitive22Na+-uptake into Na+-loaded cells. Both results suggest the presence of a Na+/H+ antiport. (2) When alkalinization of the cells was induced by preincubation with 50 mmol/l acetate in HCO 3 − -Ringer's and subsequent removal of the weak acid, the following regulation was dependent on the presence of extracellular chloride. This process could be blocked with DIDS (1 mmol/l), suggesting the presence of a Cl−/HCO 3 − exchange mechanism. (3) We found no evidence for a Na+/HCO 3 − -cotransport, which had been postulated to be present in RPE by others. We conclude that two processes are involved in regulation of pHi in RPE: A Na+/H+ antiport responsible for recovery of pHi from acid load, and a DIDS-sensitive Cl−/HCO 3 − exchange mechanism responsible for recovery of pHi after alkalinization.
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  • 4
    ISSN: 1432-1424
    Keywords: intracellular pH ; sodium bicarbonate cotransport ; Na+/H+ antiport ; Cl−/HCO 3 − exchange ; amiloride ; DIDS ; cornea ; endothelium ; cell culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Intracellular pH (pH i ) in confluent monolayers of cultured bovine corneal endothelial cells was determined using the pH-dependent absorbance of intracellularly trapped 5(and 6)carboxy-4′,5′-dimethylfluorescein. Steady-state pH was 7.05±0.1 in the nominal absence of bicarbonate, and 7.15±0.1 in the presence of 28mm HCO 3 − /5% CO2. Following an acid load imposed by a NH4Cl prepulse, pH i was regulated in the absence of HCO 3 − by a Na+-dependent process inhibitable to a large extent by 1mm amiloride and 0.1mm dimethylamiloride. In the presence of 28mm HCO 3 − /5% CO2, this regulation was still dependent on Na+, but the inhibitory potency of amiloride was less. DIDS (1mm) partially inhibited this regulation in the presence, but not in the absence of bicarbonate. With cells pretreated with DIDS, amiloride was as effective in inhibiting recovery from acid load as in the absence of HCO 3 − . The presence of intracellular Cl− did not appreciably affect this recovery, which was still sensitive to DIDS in the absence of Cl−. Removal of extracellular Na+ led to a fall of pH i , which was greatly attenuated in the absence of HCO 3 − . This acidification was largely reduced by 1mm DIDS, but not by amiloride. Cl removal led to an intracellular alkalinization in the presence of HCO 3 − . The presence of a Cl−/HCO 3 − exchanger was supported by demonstrating DIDS-sensitive36Cl− uptake into confluent cell monolayers. Thus, bovine corneal endothelial cells express three processes involved in intracellular pH regulation: an amiloride-sensitive Na+/H− antiport, a Na−−HCO 3 − symport and a Cl−/HCO 3 − exchange, the latter two being DIDS sensitive.
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