Palytoxin-induced cell death cascade in bovine aortic endothelial cells

The plasmalemmal Na⁺-K⁺-ATPase (NKA) pump is the receptor for the potent marine toxin palytoxin (PTX). PTX binds to the NKA and converts the pump into a monovalent cation channel that exhibits a slight permeability to Ca²⁺. However, the ability of PTX to directly increase cytosolic free Ca²⁺ concentration ([Ca²⁺]_i) via Na⁺ pump channels and to initiate Ca²⁺ overload-induced oncotic cell death has not been examined. Thus the purpose of this study was to determine the effect of PTX on [Ca²⁺]_i and the downstream events associated with cell death in bovine aortic endothelial cells. PTX (3–100 nM) produced a graded increase in [Ca²⁺]_i that was dependent on extracellular Ca²⁺. The increase in [Ca²⁺]_i initiated by 100 nM PTX was blocked by pretreatment with ouabain with an IC₅₀ < 1 µM. The elevation in [Ca²⁺]_i could be reversed by addition of ouabain at various times after PTX, but this required much higher concentrations of ouabain (0.5 mM). These results suggest that the PTX-induced rise in [Ca²⁺]_i occurs via the Na⁺ pump. Subsequent to the rise in [Ca²⁺]_i, PTX also caused a concentration-dependent increase in uptake of the vital dye ethidium bromide (EB) but not YO-PRO-1. EB uptake was also blocked by ouabain added either before or after PTX. Time-lapse video microscopy showed that PTX ultimately caused cell lysis as indicated by release of transiently expressed green fluorescent protein (molecular mass 27 kDa) and rapid uptake of propidium iodide. Cell lysis was 1) greatly delayed by removing extracellular Ca²⁺ or by adding ouabain after PTX, 2) blocked by the cytoprotective amino acid glycine, and 3) accompanied by dramatic membrane blebbing. These results demonstrate that PTX initiates a cell death cascade characteristic of Ca²⁺ overload. necrosis; vital dyes; membrane blebs; time-lapse video microscopy; fura-2     

Maitotoxin activates a nonselective cation channel and a P2Z/P2X7-like cytolytic pore in human skin fibroblasts

Maitotoxin (MTX),a potent cytolytic agent, activatesCa²⁺ entry via nonselective cationchannels in virtually all types of cells. The identity of the channelsinvolved and the biochemical events leading to cell lysis remainunknown. In the present study, the effect of MTX on plasmalemmalpermeability of human skin fibroblasts was examined. MTX produced atime- and concentration-dependent increase in cytosolic freeCa²⁺ concentration that dependedon extracellular Ca²⁺ and wasrelatively insensitive to blockade by extracellular lanthanides. MTXalso produced a time- and concentration-dependent increase inplasmalemma permeability to larger molecules as indicated by 1) uptake of ethidium (314 Da),2) uptake of YO-PRO-1 (375 Da), 3) release of intracellular fura 2 (636 Da), 4) uptake of POPO-3 (715 Da), and, ultimately,5) release of lactate dehydrogenase (relative molecular weight of 140,000). At the single cell level, uptake of YO-PRO-1 correlated in time with the appearance of large MTX-induced membrane currents carried by the organic cation,N-methyl-D-glucamine (167 Da). Thus MTX initially activatesCa²⁺-permeable cation channels andlater induces the formation of large pores. These effects of MTX onplasmalemmal permeability are similar to those seen on activation ofP2Z/P2X₇ receptors ina variety of cell types, raising the intriguing possibility that MTXand P2Z/P2X₇ receptor stimulationactivate a common cytolytic pore.

     

Blockade of maitotoxin-induced endothelial cell lysis by glycine and L-alanine

The maitotoxin (MTX)-induced cell deathcascade in bovine aortic endothelial cells (BAECs) is a model foroncotic/necrotic cell death. The cascade is initiated by an increase incytosolic free Ca²⁺ concentration([Ca²⁺]_i), which is followed by the biphasicuptake of vital dyes. The initial phase of dye entry reflectsactivation of large pores and correlates with surface membrane blebformation; the second phase reflects cell lysis. In the present study,the effect of the cytoprotective amino acid glycine was examined.Glycine had no effect on MTX-induced change in[Ca²⁺]_i or on the first phase of vital dyeuptake but produced a concentration-dependent (EC₅₀ ~1mM) inhibition of the second phase of dye uptake. No cytoprotectiveeffect was observed with L-valine, L-proline,or D-alanine, whereas L-alanine wasequieffective to glycine. Furthermore, glycine had no effect onMTX-induced bleb formation. To test the hypothesis that glycinespecifically blocks formation of a lytic "pore," the loss offluorescence from BAECs transiently expressing GFP and concatemers ofGFP ranging in size from 27 to 162 kDa was examined using time-lapsevideomicroscopy. MTX-induced loss of GFP was rapid, correlated with thesecond phase of dye uptake, and was relatively independent of molecularsize. The MTX-induced loss of GFP from BAECs was completely blocked byglycine. The data suggest that the second "lytic" phase ofMTX-induced endothelial cell death reflects formation of a novelpermeability pathway that allows macromolecules such as GFP or LDH toescape, yet can be prevented by the cytoprotective agents glycine andL-alanine.

     

Blockade of maitotoxin-induced oncotic cell death reveals zeiosis

Background  

Maitotoxin (MTX) initiates cell death by sequentially activating 1) Ca²⁺ influx via non-selective cation channels, 2) uptake of vital dyes via formation of large pores, and 3) release of lactate dehydrogenase, an indication of cell lysis. MTX also causes formation of membrane blebs, which dramatically dilate during the cytolysis phase. To determine the role of phospholipase C (PLC) in the cell death cascade, U73122, a specific inhibitor of PLC, and U73343, an inactive analog, were examined on MTX-induced responses in bovine aortic endothelial cells.     

The Involvement of Calcium Ions in Maintenance of Apple Fruit Tissue 9

The hypothesis that the cell walls of apple fruit tissue arebound together by Ca²⁺ ions was tested by infiltration withother cations of similar size. Sr²⁺ and Ba²⁺ were as effectiveas Ca²⁺ in increasing the resistance of apple tissue to failureunder tension while Mg²⁺, Sm³⁺, La³⁺ and Ce³⁺ were less effective.Infiltration with Ca²⁺ increased the tensile strength of tissuefrom air-stored apples to 85% of that of untreated CA-storedfruit. It was concluded that both movement of Ca²⁺ from themiddle lamella and loss of its binding sites occurred duringapple softening, with the movement of Ca²⁺ predominating andthat these processes contribute to changes in tissue structure. Substitution of D₂O for H₂O in infiltration solutions did notaffect the strength of tissue. Key words: Calcium ions, apple fruit, cell walls     

Maitotoxin-induced membrane blebbing and cell death in bovine aortic endothelial cells

Background

Maitotoxin, a potent cytolytic agent, causes an increase in cytosolic free Ca²⁺ concentration ([Ca²⁺]_i) via activation of Ca²⁺-permeable, non-selective cation channels (CaNSC). Channel activation is followed by formation of large endogenous pores that allow ethidium and propidium-based vital dyes to enter the cell. Although activation of these cytolytic/oncotic pores, or COP, precedes release of lactate dehydrogenase, an indication of oncotic cell death, the relationship between CaNSC, COP, membrane lysis, and the associated changes in cell morphology has not been clearly defined. In the present study, the effect maitotoxin on [Ca²⁺]_i, vital dye uptake, lactate dehydrogenase release, and membrane blebbing was examined in bovine aortic endothelial cells.

Results

Maitotoxin produced a concentration-dependent increase in [Ca²⁺]_i followed by a biphasic uptake of ethidium. Comparison of ethidium (M_w 314 Da), YO-PRO-1 (M_w 375 Da), and POPO-3 (M_w 715 Da) showed that the rate of dye uptake during the first phase was inversely proportional to molecular weight, whereas the second phase appeared to be all-or-nothing. The second phase of dye uptake correlated in time with the release of lactate dehydrogenase. Uptake of vital dyes at the single cell level, determined by time-lapse videomicroscopy, was also biphasic. The first phase was associated with formation of small membrane blebs, whereas the second phase was associated with dramatic bleb dilation.

Conclusions

These results suggest that maitotoxin-induced Ca²⁺ influx in bovine aortic endothelial cells is followed by activation of COP. COP formation is associated with controlled membrane blebbing which ultimately gives rise to uncontrolled bleb dilation, lactate dehydrogenase release, and oncotic cell death.     

Maitotoxin and P2Z/P2X7 purinergic receptor stimulation activate a common cytolytic pore

The effects ofmaitotoxin (MTX) on plasmalemma permeability are similar to thosecaused by stimulation of P2Z/P2X₇ionotropic receptors, suggesting that1) MTX directly activatesP2Z/P2X₇ receptors or2) MTX andP2Z/P2X₇ receptor stimulationactivate a common cytolytic pore. To distinguish between these twopossibilities, the effect of MTX was examined in1) THP-1 monocytic cells before andafter treatment with lipopolysaccharide and interferon-, a maneuverknown to upregulate P2Z/P2X₇receptor, 2) wild-type HEK cells andHEK cells stably expressing theP2Z/P2X₇ receptor, and3) BW5147.3 lymphoma cells, a cellline that expresses functional P2Z/P2X₇ channels that are poorlylinked to pore formation. In control THP-1 monocytes, addition of MTXproduced a biphasic increase in the cytosolic freeCa²⁺ concentration([Ca²⁺]_i);the initial increase reflects MTX-inducedCa²⁺ influx, whereas the secondphase correlates in time with the appearance of large pores and theuptake of ethidium. MTX produced comparable increases in[Ca²⁺]_iand ethidium uptake in THP-1 monocytes overexpressing theP2Z/P2X₇ receptor. In bothwild-type HEK and HEK cells stably expressing theP2Z/P2X₇ receptor, MTX-inducedincreases in[Ca²⁺]_iand ethidium uptake were virtually identical. The response of BW5147.3cells to concentrations of MTX that produced large increases in[Ca²⁺]_ihad no effect on ethidium uptake. In both THP-1 and HEK cells, MTX- andBz-ATP-induced pores activate with similar kinetics and exhibit similarsize exclusion. Last, MTX-induced pore formation, but not channelactivation, is greatly attenuated by reducing the temperature to22°C, a characteristic shared by theP2Z/P2X₇-induced pore. Together,the results demonstrate that, although MTX activates channels that aredistinct from those activated byP2Z/P2X₇ receptor stimulation, thecytolytic/oncotic pores activated by MTX- and Bz-ATP are indistinguishable.

     

Hypotonic swelling stimulates L-type Ca2+ channel activity in vascular smooth muscle cells through PKC

It has been suggested that L-type Ca²⁺ channels play an important role in cell swelling-induced vasoconstriction. However, there is no direct evidence that Ca²⁺ channels in vascular smooth muscle are modulated by cell swelling. We tested the hypothesis that L-type Ca²⁺ channels in rabbit portal vein myocytes are modulated by hypotonic cell swelling via protein kinase activation. Ba²⁺ currents (I_Ba) through L-type Ca²⁺ channels were recorded in smooth muscle cells freshly isolated from rabbit portal vein with the conventional whole cell patch-clamp technique. Superfusion of cells with hypotonic solution reversibly enhanced Ca²⁺ channel activity but did not alter the voltage-dependent characteristics of Ca²⁺ channels. Bath application of selective inhibitors of protein kinase C (PKC), Ro-31–8425 or Go-6983, prevented I_Ba enhancement by hypotonic swelling, whereas the specific protein kinase A (PKA) inhibitor KT-5720 had no effect. Bath application of phorbol 12,13-dibutyrate (PDBu) significantly increased I_Ba under isotonic conditions and prevented current stimulation by hypotonic swelling. However, PDBu did not have any effect on I_Ba when cells were first exposed to hypotonic solution. Furthermore, downregulation of endogenous PKC by overnight treatment of cells with PDBu prevented current enhancement by hypotonic swelling. These data suggest that hypotonic cell swelling can enhance Ca²⁺ channel activity in rabbit portal vein smooth muscle cells through activation of PKC. cell swelling; protein kinases; calcium current     

Bidirectional Ca2+ coupling of mitochondria with the endoplasmic reticulum and regulation of multimodal Ca2+ entries in rat brown adipocytes

How the endoplasmic reticulum (ER) and mitochondria communicate with each other and how they regulate plasmalemmal Ca²⁺ entry were studied in cultured rat brown adipocytes. Cytoplasmic Ca²⁺ or Mg²⁺ and mitochondrial membrane potential were measured by fluorometry. The sustained component of rises in cytoplasmic Ca²⁺ concentration ([Ca²⁺]_i) produced by thapsigargin was abolished by removing extracellular Ca²⁺, depressed by depleting extracellular Na⁺, and enhanced by raising extracellular pH. FCCP, dinitrophenol, and rotenone caused bi- or triphasic rises in [Ca²⁺]_i, in which the first phase was accompanied by mitochondrial depolarization. The FCCP-induced first phase was partially inhibited by oligomycin but not by ruthenium red, cyclosporine A, U-73122, a Ca²⁺-free EGTA solution, and an Na⁺-free solution. The FCCP-induced second phase paralleling mitochondrial repolarization was partially blocked by removing extracellular Ca²⁺ and fully blocked by oligomycin but not by thapsigargin or an Na⁺-deficient solution, was accompanied by a rise in cytoplasmic Mg²⁺ concentration, and was summated with a high pH-induced rise in [Ca²⁺]_i, whereas the extracellular Ca²⁺-independent component was blocked by U-73122 and cyclopiazonic acid. The FCCP-induced third phase was blocked by removing Ca²⁺ but not by thapsigargin, depressed by decreasing Na⁺, and enhanced by raising pH. Cyclopiazonic acid-evoked rises in [Ca²⁺]_i in a Ca²⁺-free solution were depressed after FCCP actions. Thus mitochondrial uncoupling causes Ca²⁺ release, activating Ca²⁺ release from the ER and store-operated Ca²⁺ entry, and directly elicits a novel plasmalemmal Ca²⁺ entry, whereas Ca²⁺ release from the ER activates Ca²⁺ accumulation in, or release from, mitochondria, indicating bidirectional mitochondria-ER couplings in rat brown adipocytes. plasmalemmal calcium entry; calcium release; mitochondrial depolarization; FCCP     

Sustained norepinephrine contraction in the rat portal vein is lost when Ca(2+) is replaced with Sr(2+)

Agonist-induced activation of smoothmuscle involves a rise in intracellular Ca²⁺ concentrationand sensitization of myosin light chain phosphorylation toCa²⁺. Sr²⁺ can enter through Ca²⁺channels, be sequestered and released from sarcoplasmic reticulum, andreplace Ca²⁺ in activation of myosin light chainphosphorylation. Sr²⁺ cannot replace Ca²⁺ infacilitation of agonist-activated Ca²⁺-dependentnonselective cation channels. It is not known whether Sr²⁺can replace Ca²⁺ in small G protein-mediated sensitizationof phosphorylation. To explore mechanisms involved in-receptor-activated contractions in smooth muscle, effects ofreplacing Ca²⁺ with Sr²⁺ were examined in ratportal vein. Norepinephrine (NE) at >3.0 × 10⁷ Min the presence of Ca²⁺ resulted in a strong sustainedcontraction, whereas this sustained component was absent in thepresence of Sr²⁺; only the amplitude of phasic contractionsincreased. Pretreatment with low (~0.05 mM) free Ca²⁺followed by 2.5 mM Sr²⁺ resulted in a sustained componentof the NE response. In -escin-permeabilized preparations,phenylephrine in the presence of GTP or guanosine 5'-O-(3-thiotriphosphate) alone induced sensitization toSr²⁺. In conclusion, a Ca²⁺-regulatedmembrane/channel process is required for the sustained component of NEresponses in rat portal vein. Sensitization alone is not responsiblefor the sustained phase of the NE contraction.

     

Zinc Absorption by Wheat Seedlings and the Nature of its Inhibition by Alkaline Earth Cations

The effects and interactions of the alkaline earth cations onZn²⁺ absorption were studied in. short-term experiments. Atlow concentrations of Zn²⁺ ( 2 µM), rates of Zn²⁺ absorptionwere linear even in the absence of Ca²⁺ or of other cations.At higher Zn²⁺ concentrations (5 and 10µm), rates werenot linear in the absence of other cations but became linearon addition of 250 µM or more of Ca²⁺, Mg²⁺, Sr²⁺, orBa²⁺. From 0.1 to 10µM Zn²⁺, all alkaline earth cations inhibitedabsorption in the order Mg²⁺ > Ba²⁺ Sr²⁺ = Ca²⁺. Increasingconcentrations of Ca²⁺ or of Mg²⁺ from 0 to 40 mM progressivelydepressed absorption from 1µM ZnCl₂. Increasing Ca²⁺ orMg²⁺ from 40 to 100 mM had no further effect on absorption.Over both high and low ranges of Ca²⁺ or Mg²⁺ concentrations,the affinity of plant roots for Zn²⁺ and the responses of Zn²⁺absorption to temperature, H⁺, and Cu²⁺ were identical. At equalconcentrations over the whole concentration range, Mg²⁺ was30 per cent more effective than Ca²⁺ in inhibiting absorption.At concentrations below 40 mM, Ca²⁺ and Mg²⁺ competed with eachother in their inhibiting effects. At concentrations above 40mM, Ca²⁺ alleviated the extra inhibitory effects of Mg²⁺ insome unknown way. The alkaline earth cations inhibited Zn²⁺ absorption non-competitively.They depressed it to values which would limit vigorous plantgrowth. It is postulated that their effects are important inthe zinc nutrition of plants in soil and in solution cultures.     

Effects of Divalent Cations on the Excitability and on the Cytoplasmic Streaming of Chara corallina

The plasmalemma of Chara corallina remained excitable, whenit was treated with 1 to 100 µM of TFP. However, excitationcessation (EC) uncoupling, i.e. no cessation of cytoplasmicstreaming during an action potential, was observed in a concentrationrange of TFP between 30 to 100 µM. The percentage of occurrenceof the EC-uncoupling increased with the concentration of TFP.The EC-uncoupling effect of TFP could be removed by externalperfusion with 0.1 min or higher concentration of Ca²⁺ but notwith Mg²⁺, Ba²⁺, Sr²⁺ or Pb²⁺. These results suggest that excitationof the plasmalemma and EC-coupling is regulated via calmodulinor calmodulin-like system. (Received December 15, 1986; Accepted April 4, 1987)     

Passive Interactions of Ca2+ and other Multivalent Cations with the Membranes of Isolated Corn Mitochondria

The presence of Ca²⁺ in a hypo-osmotic reaction medium reducessuccinate: cytochrome c reductase activity and the release ofouter membrane-specific antimycin A-insensitive NADH: cytochromec reductase. The action of Ca²⁺ is non-competitive and approximately30 mmol m^–3 Ca²⁺ affords half-maximal (I₅₀) protection.The effect of a range of inorganic and organic multivalent cationson succinate: cytochrome c reductase activity suggests thatthe action of Ca²⁺ is non-specific and probably involves Ca²⁺binding to outer membrane component(s) which may be proteins. Valinomycin- or gramicidin-induced passive swelling of isolatedcorn mitochondria in isotonic K.C1 is also non-competitivelyinhibited by up to 50% with Ca²⁺. Half-maximal inhibition (I₅₀)occurs at 0-35 mol m^–3 Ca²⁺ for valinomycin and 1-0 molm^–3 Ca²⁺ for gramicidin. Other divalent cations, Mg²⁺,Sr²⁺ and Ba²⁺, seem to inhibit similarly while the trivalentcations La³⁺ and Ho³⁺ show a maximum inhibition of up to 85%,with an I₅₀ of 0.1 mol m^–3 for valinomycin. It is suggestedthat non-specific cation binding may reduce membrane fluiditythereby slowing down the rate of ionophore penetration throughthe inner membrane. Key words: Calcium, Mitochondria, Membranes     

25-Hydroxysterols increase the permeability of liposomes to Ca2+ and other cations

25-Hydroxycholesterol and 25-hydroxy vitamin D-3 increased the permeability of liposomes to Ca²⁺ measured by the arsenazo III encapsulation technique. This effect was sensitive to the lipid composition of the membrane, with changes that decreased the motional freedom of phospholipid acyl chains decreasing Ca²⁺ permeability. The greatest permeability was observed with the zwitter-ionic phospholipids, phosphatidylcholine and phosphatidylethanolamine, whereas the acidic phospholipids, phosphatidylinositol and phosphatidylserine, depressed Ca²⁺ permeability. The effect was not specific for Ca²⁺. Other divalent cations were translocated in the order Mn²⁺ > Mg²⁺  Ca²⁺ ? Sr²⁺  Ba²⁺. The permeability of liposomes to the monovalent cation, Na⁺, was also substantially increased. The effect did not appear to be due to ionophoretic properties of the sterols, and it is suggested that perturbation of the membranes by the polar 25-hydroxyl group may play a role in increasing membrane permeability.     

Calmodulin and protein kinase C regulate gap junctional coupling in lens epithelial cells

The mechanisms regulating the permeability of lens epithelial cell gap junctions in response to calcium ionophore or ATP agonist-mediated increases in cytosolic Ca²⁺ (Ca_i²⁺) have been investigated using inhibitors of calmodulin (CaM) and PKC. Cell-to-cell transfer of the fluorescent dye AlexaFluor594 decreased after the rapid and sustained increase in Ca_i²⁺ (to micromolar concentrations) observed after the addition of ionophore plus Ca²⁺ but was prevented by pretreatment with inhibitors of CaM but not PKC. In contrast, the delayed, transient decrease in cell-to-cell coupling observed after the addition of ATP that we have reported previously (Churchill G, Lurtz MM, and Louis CF. Am J Physiol Cell Physiol 281: C972-C981, 2001) could be prevented by either the direct or indirect inhibition of PKC but not by inhibition of CaM. Surprisingly, there was no change in the relative proportion of the different phosphorylated forms of lens connexin43 after this ATP-dependent transient decrease in cell-to-cell coupling. Although BAPTA-loaded cells did not display the ATP-dependent transient increase in Ca_i²⁺, the delayed, transient decrease in cell-to-cell dye transfer was still observed, indicating it was Ca_i²⁺ independent. Thus CaM-mediated inhibition of lens gap junctions is associated with sustained, micromolar Ca_i²⁺ concentrations, whereas PKC-mediated inhibition of lens gap junctions is associated with agonist activation of second messenger pathways that are independent of changes in Ca_i²⁺. calcium; connexin43; lens gap junctions     

MHC isoform composition and Ca(2+)- or Sr(2+)-activation properties of rat skeletal muscle fibers

Chemically skinned single fibers from adult rat skeletalmuscles were used to test the hypothesis that, in mammalian muscle fibers, myosin heavy chain (MHC) isoform expression andCa²⁺- or Sr²⁺-activation characteristics areonly partly correlated. The fibers were first activated inCa²⁺- or Sr²⁺-buffered solutions undernear-physiological conditions, and then their MHC isoform compositionwas determined electrophoretically. Fibers expressing only the MHC Iisoform could be appropriately identified on the basis of either theCa²⁺- or Sr²⁺-activation characteristics or theMHC isoform composition. Fibers expressing one or a combination of fastMHC isoforms displayed no significant differences in theirCa²⁺- or Sr²⁺-activation properties; therefore,their MHC isoform composition could not be predicted from theirCa²⁺- or Sr²⁺-activation characteristics. Alarge proportion of fibers expressing both fast- and slow-twitch MHCisoforms displayed Ca²⁺- or Sr²⁺-activationproperties that were not consistent with their MHC isoform composition;thus both fiber-typing methods were needed to fully characterize suchfibers. These data show that, in rat skeletal muscles, the extent ofcorrelation between MHC isoform expression and Ca²⁺- orSr²⁺-activation characteristics is fiber-type dependent.

     

Metal Selectivity of Exocytosis in α-Toxin-Permeabilized Bovine Chromaffin Cells

Abstract: Metal selectivity of exocytosis was analyzed by comparing the effects of polyvalent metal cations Ca²⁺, Ba²⁺, Sr²⁺, Pb²⁺, La³⁺, Cd²⁺, Co²⁺, Tb³⁺, Mn²⁺, and Zn²⁺ on the release of norepinephrine (NE) from staphylococcal α-toxin-permeabilized bovine chromaffin cells. Pb²⁺, La³⁺, Cd²⁺, Sr²⁺, and Ba²⁺ activated NE secretion accompanied by the release of intragranular dopamine β-hydroxylase but not cytosolic lactate dehydrogenase, indicating the activation of the mechanism of exocytosis. The release triggered by saturating concentrations of Pb²⁺, La³⁺, Cd²⁺, and Sr²⁺ was nonadditive with Ca²⁺, indicating a common site of action. In contrast, the Ba²⁺-evoked NE release was additive with Ca²⁺ and the Ca²⁺ agonists Pb²⁺, La³⁺, Cd²⁺, and Sr²⁺, suggesting that Ba²⁺ activates secretion at a site distinct from the Ca²⁺ receptor. In distinction to the NE release evoked by Pb²⁺, La³⁺, Cd²⁺, and Ba²⁺, the Sr²⁺-evoked NE release was associated with a significant elevation of Ca²⁺ concentration in the medium and abolished by Ca²⁺ chelation. This indicates that the secretagogue effect of Sr²⁺ was indirect and secondary to the displacement of bound Ca²⁺. Co²⁺ and Mn²⁺ inhibited the NE release evoked by Ca²⁺, Sr²⁺, Pb²⁺, La³⁺, and Cd²⁺ but had no effect on the Ba²⁺-dependent secretion. Tb³⁺ and Zn²⁺ were without effect on exocytosis.     

Regulation of Na+/Ca2+ exchange activity by cytosolic Ca2+ in transfected Chinese hamster ovary cells

Transfected Chinese hamster ovary cells stably expressing thebovine cardiacNa⁺/Ca²⁺exchanger (CK1.4 cells) were used to determine the range of cytosolic Ca²⁺ concentrations([Ca²⁺]_i)that activateNa⁺/Ca²⁺exchange activity. Ba²⁺ influx wasmeasured in fura 2-loaded, ionomycin-treated cells under conditions inwhich the intracellular Na⁺concentration was clamped with gramicidin at ~20 mM.[Ca²⁺]_iwas varied by preincubating ionomycin-treated cells with either theacetoxymethyl ester of EGTA or medium containing 0-1 mM added CaCl₂. The rate ofBa²⁺ influx increased in asaturable manner with[Ca²⁺]_i,with the half-maximal activation value of 44 nM and a Hill coefficientof 1.6. When identical experiments were carried out with cellsexpressing a Ca²⁺-insensitivemutant of the exchanger, Ba²⁺influx did not vary with[Ca²⁺]_i.The concentration for activation of exchange activity was similar tothat reported for whole cardiac myocytes but approximately an order ofmagnitude lower than that reported for excised, giant patches. Thereason for the difference in Ca²⁺regulation between whole cells and membrane patches is unknown.

     

Divalent cation stimulation of substrate oxidation by corn mitochondria

The oxidation of reduced nicotinamide adenine dinucleotide, malate-pyruvate, and succinate by corn mitochondria in buffered 0.2 m KCl was determined as a function of divalent cations. Ni²⁺, Mg²⁺, Co²⁺, Ca²⁺, Mn²⁺, Sr²⁺, and Ba²⁺ stimulated reduced nicotinamide adenine dinucleotide oxidation in the absence of inorganic phosphate, with Ca²⁺ and Sr²⁺ having the greatest effect. Malate-pyruvate and succinate oxidation was stimulated by Ca²⁺, Ba²⁺, and Sr²⁺, but only in the presence of inorganic phosphate. Ca²⁺, Sr²⁺, and Ba²⁺ produced a simulated state 4 to state 3 transition with all three substrates, but only with malate-pyruvate and succinate was there a return to state 4. The order of divalent cation effectiveness suggests that the rate of water substitution from the cation inner coordination hydration sphere may be a rate-limiting step in certain mitochondrial reactions involving electron transport and phosphorylation.     

Cations Residing at the Selectivity Filter of the Voltage-Gated Ca2+-Channel Modify Fusion-Pore Kinetics

Strontium (Sr²⁺), Barium (Ba²⁺), and Lanthanum (La³⁺) can substitute for Ca²⁺ in driving synaptic transmission during membrane depolarization. Ion recognition at the polyglutamate motif (EEEE), comprising the channel selectivity-filter, during voltage-driven transitions, controls the kinetics of the voltage-gated calcium channel (VGCC) and its interactions with the synaptic proteins. We tested the effect of different charge carriers on evoked-release, as a means of exploring the involvement of VGCC in the fusion pore configuration. Employing amperometry recordings in single bovine chromaffin cells we show that the size of the fusion pore, designated by the 'foot'-amplitude, was increased when Ba²⁺ substituted for Ca²⁺ and decreased, with La³⁺. The fusion pore stability, indicated by 'foot'-width, was decreased in La³⁺. Also, the mean open time of the fusion pore (tfp) was significantly lower in Sr²⁺ and La³⁺ compared to Ba²⁺ and Ca²⁺. These cations when occupying the selectivity filter reduced the spike frequency in the order of Ca²⁺ > Sr²⁺ > Ba²⁺ > La³⁺, which is parallel to the reduction in total catecholamine release. The correlation between ion binding at the selectivity filter and fusion pore properties supports a model in which the Ca²⁺ channel regulates secretion through a site at the selectivity filter, upstream to cation entry into the cell.