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  • Cell culture  (5)
  • cell culture  (5)
  • Cl−/HCO 3 − exchange  (2)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    The journal of membrane biology 99 (1987), S. 173-186 
    ISSN: 1432-1424
    Schlagwort(e): ciliary body ; cell culture ; intracellular potentials ; K+ conductance ; Na+/K+-ATPase ; ouabain
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: Summary Using intracellular microelectrode technique, we investigated the changes in membrane voltage (V) of cultured bovine pigmented ciliary epithelial cells induced by different extracellular solutions. (1)V in 213 cells under steady-state conditions averaged −46.1±0.6 mV (sem). (2) Increasing extracellular K+ concentration ([K+] o ) depolarizedV. Addition of Ba2+ could diminish this response. (3) Depolarization on doubling [K+] o was increased at higher [K+] o (or low voltage). (4) Removing extracellular Ca2+ decreasedV and reduced theV amplitude on increasing [K+] o . (5)V was pH sensitive. Extra-and intracellular acidification depolarizedV; alkalinization induced a hyperpolarization.V responses to high [K+] o were reduced at acidic extracellular pH. (6) Removing K o + depolarized, K o + readdition after K+ depletion transiently hyperpolarizedV. These responses were insensitive to Ba2+ but were abolished in the presence of ouabain or in Na+-free medium. (7) Na+ readdition after Na+ depletion transiently hyperpolarizedV. This reaction was markedly reduced in the presence of ouabain or in K+-free solution but unchanged by Ba2+. It is concluded that in cultured bovine pigmented ciliary epithelial cells K+ conductance depends on Ca2+, pH and [K+] o (or voltage). An electrogenic Na+/K+-transport is present, which is stimulated during recovery from K+ or Na+ depletion. This transport is inhibited by ouabain and in K+-or Na+-free medium.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Pflügers Archiv 405 (1985), S. S167 
    ISSN: 1432-2013
    Schlagwort(e): Corneal endothelium ; Cell culture ; Intracellular potential ; Sodium-bicarbonate cotransport ; pH regulation ; Stilbenes
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Intracellular potential measurements on confluent monolayers of cultured bovine corneal endothelial cells were used to define passive ion transport processes in these cells. Previous studies [11, 12] have provided the experimental basis for a cellular model, is which bicarbonate entry across the basolateral membrane in indirectly driven by a Na+/H+-exchanger, which is inhibitable by amiloride (1 mmol/l). Na+ and HCO 3 − leave the cell via an electrogenic bicarbonate sodium cotransport, which is inhibitable by the disulfonic stilbene derivates SITS or DIDS. This model is also compatible with transepithelial work from other groups. In this paper, we briefly review the evidence we have obtained for this model.
    Materialart: Digitale Medien
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  • 3
    ISSN: 1432-2013
    Schlagwort(e): Ciliary muscle ; Cell culture ; Intracellular calcium ; Isolated ciliary muscle strips ; Contractility ; Acetylcholine ; Carbachol
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Electromechanical and pharmacomechanical coupling was investigated in human ciliary muscle by measuring the intracellular free calcium in single cultured ciliary muscle cells and the contractility in meridional ciliary muscle strips. The basal resting calcium concentration was 75±8.7 nmol/l, n=23. Application of acetylcholine (0.1 mmol/l) and carbachol (0.1 mmol/l) resulted in an initial [Ca2+]i peak followed by a recovery phase and a [Ca2+]i plateau. The initial [Ca2+]i peak was still observed in the absence of extracellular calcium and in the presence of verapamil (0.1 mmol/l). During its plateau [Ca2+]i was decreased by withdrawal of extracellular calcium or application of verapamil (0.1 mmol/l). Depolarization induced by a high level of extracellular potassium yielded only a small transient [Ca2+]i peak without a [Ca2+]i plateau. In isolated ciliary muscle strips, muscarinic stimulation (carbachol 0.1 mmol/l) resulted in an initial phasic and a subsequent tonic contraction. Removal of external calcium reduced the phasic contraction to 30.6±4.4% (n=8) and completely abolished the tonic one. Verapamil (0.1 mmol/l) had only a slight relaxing effect when applied during the tonic contraction. We conclude that human ciliary muscle contraction is mediated by calcium release from intracellular stores and calcium entry through calcium channels, which are most probably receptor-operated. Depolarization of the muscle cell membrane and calcium entry through voltage-operated calcium channels do not contribute significantly to human ciliary muscle contraction.
    Materialart: Digitale Medien
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  • 4
    ISSN: 1432-2013
    Schlagwort(e): Human ciliary muscle ; Smooth muscle ; Cell culture ; Intracellular calcium ; Membrane potential ; Acetylcholine ; Endothelin
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract We characterized the effects of acetylcholine and endothelin on cultured human ciliary muscle cells, using the calcium-sensitive dye fura-2 to measure intracellular calcium and intracellular microelectrodes to measure the membrane potential. Both agonists, endothelin and acetylcholine, had a typcial biphasic effect on the intracellular calcium concentration. Calcium peaked initially, because of its release from intracellular stores, and then reached a plateau, owing to entry of extracellular calcium. Endothelin-induced calcium entry was almost completely blocked by addition of extracellular La3+ (50 μmol/l) and Ni2+ (1 mmol/l). Acetylcholine-induced calcium entry was likewise almost completely abolished by La3+ and Ni2+. Both endothelin and acetylcholine led to an initial transient hyperpolarization with a subsequent depolarization. The hyperpolarization of the membrane potential had a time course similar to the initial calcium peak, while the depolarization occurred parallel to the calcium plateau. The depolarization induced by both agonists was reduced in the presence of La3+ and Ni2+. Verapamil (10 μmol/l) had no effect on either the calcium entry or the depolarization. Acetylcholine did not induce a [Ca2+]i peak when it was applied during the endothelin-induced [Ca2+]i plateau and vice versa. The [Ca2+]i plateau was not higher with concomitant than with single application of acetylcholine or endothelin. Thus, calcium entry and membrane depolarization induced by acetylcholine and endothelin seem to be mediated by a common La3+- and Ni2+-sensitive but verapamil-insensitive mechanism.
    Materialart: Digitale Medien
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  • 5
    ISSN: 1432-2013
    Schlagwort(e): Bicarbonate ; Intracellular potentials ; Bicarbonate sodium cotransport ; Chloride ; Anion exchanger ; Cell culture ; Cornea ; Endothelium ; Furosemide ; Barium
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Using intracellular microelectrode technique, the effect of anion substitution on the voltage responses to extracellular bicarbonate and sodium was explored in cultured bovine corneal endothelial cells. 1. The overall amplitude of voltage changes induced by periodic changes of [HCO 3 − ]0 (depolarization upon removal of HCO 3 − and hyperpolarization upon readdition) was reduced when Cl− was replaced by organic anions (cyclamate, methylsulfate, benzenesulfonate) or by SO 4 2− , and to a lesser extent by substitution with Br−. 2. There was a similar effect of anion substitution on the response to changes of [Na+]0. 3. In both cases, in the absence of Cl, the voltage V returned at a slower rate to baseline levels after it had been transiently changed by either an imposed Na- or HCO3-gradient, indicating a slower dissipation of these gradients. The direct response of V to these imposed gradients was affected only to a minor degree. 4. Replacement of Cl− by SO 4 2− or organic anions led to a slow, reversible depolarization of the cell, while substitution with Br− had only a slight effect. 5. The effect of anion substitution on the voltage responses to HCO 3 − or Na+ could not be mimicked by a depolarization induced by Ba2+ (1 mM). 6. Furosemide (10−3 M) led to a slight reduction of the voltage responses to HCO 3 − , but could not suppress the effect of anion substitution on these reactions. It could neither suppress the depolarization induced by anion substitution and had no effect on steady-state PD. 7. It is suggested, that cultured bovine corneal endothelial cells, in addition to a previously demonstrated electrogenic HCO 3 − −Na+-cotransport, which is probably not dependent on Cl, possess an electroneutral mechanism for HCO 3 − and/or Na+-movement, which depends on Cl. No evidence for a Cl-conductance could be obtained.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    ISSN: 1432-2013
    Schlagwort(e): Cell culture ; pH sensitive dyes ; pH sensitive absorbance ; 5 (and 6)-carboxy-dimethylfluorescein ; Na+/H+ antiport ; Cl−/HCO 3 − exchange
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: 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.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Springer
    The journal of membrane biology 127 (1992), S. 215-225 
    ISSN: 1432-1424
    Schlagwort(e): ciliary muscle ; intracellular pH ; cell culture ; sodium-bicarbonate cotransport ; sodium/proton exchange
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: Summary We investigated intracellular pH (pH i ) regulation in cultured human ciliary muscle cells by means of the pH-sensitive absorbance of 5(and 6)-carboxy-4′,5′-dimethylfluorescein (CDMF). The steady-state pH i was 7.09±0.04 (n = 12) in CO2/ HCO 3 − -buffered and 6.86±0.03 (n = 12) in HEPES-buffered solution. Removal of extracellular sodium for 6 min acidified the cells by 1.11±0.06 pH units (n = 12) in the presence of CO2/ HCO 3 − and by 0.91±0.05 pH units (n = 8) in its absence. Readdition of external sodium resulted in a rapid pH i recovery, which was almost completely amiloride-sensitive in the absence of CO2/ HCO 3 − but only slightly influenced by amiloride in its presence. Application of DIDS under steady-state conditions significantly acidified the ciliary muscle cells by 0.25±0.02 (n = 4) in 6 min, while amiloride had no effect. The pH i recovery after an intracellular acid load was completely dependent on extracellular sodium. In HEPES-buffered solution the pH i recovery was almost completely mediated by Na+/H+ exchange, since it was blocked by amiloride (1 mmol/liter). In contrast, a marked amilorideinsensitive pH i recovery was observed in CO2/HCO 3 − -buffered solution which was mediated by chloride-independent and chloride-dependent Na+ HCO 3 − cotransport. This recovery, inhibited by DIDS (0.2 mmol/liter). was also observed if the cells were preincubated in chloride-free solution for 4 hr. Analysis of the sodium dependence of the pH i recovery after NH4Cl prepulse revealed V max = 0.57 pH units/min, K m= 39.7 mmol/liter extracellular sodium for the amiloride-sensitive component and V max = 0.19 pH units/min, K m= 14.3 mmol/liter extracellular sodium for the arniloride-insensitive component. We conclude that Na+/H+ exchange and chloride-independent and chloride-dependent Na+HCO 3 − cotransport are involved in the pH i regulation of cultured human ciliary muscle cells.
    Materialart: Digitale Medien
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  • 8
    ISSN: 1432-1424
    Schlagwort(e): corneal endothelium ; cell culture ; intracellular potential ; pH regulation ; bicarbonate ; bicarbonate-sodium cotransport ; lithium ; stilbenes ; amiloride ; ouabain
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: Summary Usin gintracellular microelectrode technique, the response of the voltageV across the plasma membrane of cultured bovine corneal endothelial cells to changes in sodium and bicarbonate concentrations was investigated. (1) The electrical response to changes in [HCO 3 − ] o (depolarization upon lowering and hyperpolarization upon raising [HCO 3 − ] o ) was dependent on sodium. Lithium could fairly well be substituted for sodium, whereas potassium or choline were much less effective. (2) Removal of external sodium caused a depolarization, while a readdition led to a hyperpolarization, which increased with time of preincubation in the sodium-depleted medium. (3) The response to changes in [Na+] o was dependent on bicarbonate. In a nominally bicarbonate-free medium, its amplitude was decreased or even reversed in sign. (4) Application of SITS or DIDS (10−3 m) had a similar effect on the response to sodium as bicarbonate-depleted medium. (5) At [Na+] o =151mm and [HCO 3 − ] o =46mm, the transients ofV depended, with 39.0±9.0 (sd) mV/decade, on bicarbonate and, with 15.3±5.8 (sd) mV/decade, on sodium. (6) After the preincubation of cells with lithium, replacement of Li by choline led to similar effects as the replacement of sodium by choline, though the response ofV was smaller with Li. This response could be reduced or reversed by the removal of bicarbonate or by the application of SITS. (7) Amiloride (10−3 m) caused a reversible hyperpolarization of the steady-state potential by 8.5±2.6 mV (sd). It did not affect the immediate response to changes in [Na+] o or [HCO 3 − ] o , but reduced the speed of regaining the steady-state potential after a change in [HCO 3 − ] o . (8) Ouabain (10−4 m) caused a fast depolarization of −6.8±1.1 (sd) mV, which was followed by a continuing slower depolarization. The effect was almost identical at 10−5 m. (9) It is suggested, that corneal endothelial cells possess a cotransport for sodium and bicarbonate, which transports net negative charage with these ions. It is inhibitable by stilbenes, but not directly affected by amiloride or ouabain. Lithium is a good substitute for sodium with respect to bicarbonate transport and is transported itself. In addition, the effect of amiloride provides indirect evidence for the existence of a Na+/H+-antiport. A model for the transepithelial transport of bicarbonate across the corneal endothelium is proposed.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    ISSN: 1432-1424
    Schlagwort(e): intracellular pH ; sodium bicarbonate cotransport ; Na+/H+ antiport ; Cl−/HCO 3 − exchange ; amiloride ; DIDS ; cornea ; endothelium ; cell culture
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: 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.
    Materialart: Digitale Medien
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  • 10
    ISSN: 1432-1424
    Schlagwort(e): corneal endothelium ; cell culture ; intracellular potential ; bicarbonate ; pH ; stilbenes
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: Summary Micropuncture of cultured bovine corneal endothelial cells led to registrations stable for hours. Intracellular potentials were mainly in the range of −40 to −55 mV, average 46.3±0.6 mV (sem). Changes of extracellular [HCO 3 − ] led to voltage transients, their amplitude depending logarithmically on [HCO 3 − ] with a mean slope of 37.3±8.8 (sd) mV. After removal of bicarbonate/CO2, a steady-state depolarization was seen. This steady-state depolarization, but not the voltage transients, could be reduced by 1mm Ba++. After removal of bicarbonate, the voltage response to changes of extracellular potassium was reduced. Alteration of pH i induced by permeable buffers (butyrate, glycodiazine and ammonium) also resulted in voltage transients, internal acidification being correlated with a hyperpolarization, and internal alkalinization with a depolarization. Also changes of external pH caused voltage responses, alkalinization causing a hyperpolarization, acidification a depolarization. Methazolamide, an inhibitor of carbonic anhydrase, as well as stilbenes (SITS or DIDS) caused a reduction of the voltage response to HCO 3 − and pH. Their effects were additive. It is suggested that corneal endothelial cells possess one or two electrogenic transporters for HCO 3 − or related species, one of which is inhibitable by stilbenes.
    Materialart: Digitale Medien
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