Is Calmodulin Involved in Electrophysiology of Chara corallina?

The role of calmodulin in Chara was investigated using the antipsychoticdrug trifluoperazine (TFP), which is known to bind to the calmodulin/Ca⁺⁺complex preventing it from carrying out its normal functions. At low concentration (4.0 µM), TFP had profound and irreversibleeffects on the electrophysiology of Chara plasmalemma. The restingp.d. depolarized and the membrane conductance decreased suggestingan inhibition of the proton pump. After several hours of exposurethe membrane became leaky, as cells deteriorated. The excitation was also affected by TFP. Spontaneous repetitivefiring was observed. The excitation increased in duration andthe action potential peak depolarized to + 20 mV. The cytoplasmic streaming was unaffected by TFP; the streamingrate at the resting potential remained unchanged when TFP wasadded to the medium, stoppage occurred at the time of excitationand the streaming slowly resumed. Key words: Calmodulin, Chara corallina, Proton pump, Cytoplasmic streaming, Current, voltage characteristics     

The electromotive force of the Chara membrane during the hyperpolarizing response

The hyperpolarizing response of the Chara internodal cell wasstudied by applying the voltage clamp and constant current techniques.By assuming the membrane as an electromotive force (emf) inseries with a resistance r (which is the sum of a series resistancer_s and the membrane resistance r_m), it was shown that the hyperpolarizingresponse was brought about not only by the increase in membraneresistance but by the increase in membrane emf. The time dependentcurrent-voltage (I–V_m) curve obtained under the voltageclamp during the hyperpolarizing response showed a negativeresistance. The hyperpolarizing response is also an excitation,since it is a transition process of the membrane across a negativeresistance region. (Received July 22, 1974; )     

Breakdown phenomena in the Chara membrane

The breakdown phenomenon in the Chara internodal cell was studiedusing the voltage clamp technique. When a slowly hyperpolarizingramp potential pulse was applied to the Chara membrane, thebreakdown occurred with hyperpolarization of about 220 mV. Thebreakdown was observed by less hyperpolarization, if the externalK⁺ concentration was increased. Such a breakdown phenomenonin the Chara membrane was caused principally by a large shiftof the membrane electromotive force toward depolarization. Thisshift frequently exceeded the peak level of the action potential. (Received July 26, 1976; )     

Tonoplast Action Potential of Characeae

The plasmalemma action potential was found to be indispensableto the production of the tonoplast action potential. In a solutionlacking Ca²⁺ and containing other divalent cations such as Ba²⁺,Mg²⁺ or Mn²⁺, the plasmalemma excited in Nitella but did notin Chara. In Nitella, however, both the tonoplast action potentialand EC-coupling were abolished due to depletion of Ca²⁺ fromthe external medium. Ca²⁺ ions injected into the cytoplasmiclayer caused a transient change in both plasmalemma and tonoplastpotentials. These results suggest that a transient rise in Ca²⁺concentration during excitation of the plasmalemma may triggerthe tonoplast action potential. (Received February 14, 1986; Accepted August 29, 1986)     

Potential dependence of the admittance ofChara plasmalemma

Summary A computer-controlled apparatus is described, which combines the two powerful methods of voltage-clamping and admittance measurement. The 5-Hz admittance ofChara plasmalemma is obtained for transmembrane PD from −400 mV to 0. DC conductance is also measured by the bipolar staircase method. Both the DC and 5-Hz conductances at steady state display a central maximum at ≈−250 mV. This feature is attributed to the conductance/voltage characteristics of the H⁺ pump. The steady-state capacitance does not show any trend throughout the potential interval. At the time of the delay, before excitation commences, the 5-Hz conductance is smaller than after excitation. At the time of excitation the 5-Hz conductance echoes the time-course of the ionic current, while the capacitance undergoes a sharp decrease followed by an increase. A possible explanation of the capacitance behavior is attempted involving transport number effects and reactances associated with the Hodgkin-Huxley gating mechanism. At punchthrough the membrane becomes inductive.     

Current-Voltage Curves for Plant Membrane Studies: A Critical Analysis of the Method

The evolution of the steady-state current-voltage (I/V) methodis followed to its present sophistication of bipolar staircase.When applied to Chara plasmalemma the resultant I/V characteristicsvary enormously depending on the physiological state of themembrane (which is, in turn, dictated by the outside conditions).This variety of response makes formulation of ‘correct’,that is artefact-free, I/V technique quite a challenge. Thetime-dependence of the clamp current in each electrophysiologicalstate is different and this must be taken into considerationwhen steady-state I/V is investigated. Clamping of the plasmalemmaalone is also necessary, as under some conditions the conductanceof the two membranes becomes similar and the effects of thetonoplast can no longer be neglected when both membranes areclamped in series. The data obtained by point clamping and spaceclamping are compared. The use of bipolar staircase introducesmore subtle artifacts: the I/V profiles can be severely misinterpreteddue to transient conductance changes arising from the excitationor the outward and inward rectifier currents. The excitationcan be blocked by temporary exposure to lanthanum ion, but theconcentration must be carefully chosen. It is necessary to optimizethe staircase parameters to allow the rectifier currents toreturn to resting level before the next staircase pulse. Finally,brief comparison of the Chara I/Vprofile to that of other cellsis included and the relevance to patch clamp studies discussed. Key words: Current-voltage characteristics, Chara, space clamp, lanthanum blockade     

Anode break excitation in Chara membrane

The anode break excitation in Chara membrane was analyzed witha model consisting of an electromotive force (emf) in serieswith a resistance r ( = l/g). The emf was found to shift towarddepolarization during supply of an inward current. Wheneverthe shift of the emf went beyond a threshold depolarization,an action potential was brought about after the end of or evenduring the inward current supply. (Received September 24, 1974; )     

Experimental Demonstration of Delayed Onset of Inactivation in the Transient Current of Nitella axilliformis

The time course for inactivation of the transient current inthe plasmalemma of Nitella axilliformis was studied. A voltageclamp that changed the membrane potential in two steps was used.Results confirmed that there is a definite delay in the inactivationprocess during excitation of the plasmalemma. (Received April 9, 1983; Accepted July 8, 1983)     

Oscillations in Extracellular Current, External pH and Membrane Potential and Conductance in the Alkaline Bands of Nitella and Chara

Oscillations with a period of approximately 2 min were observedin the membrane potential of Chara and Nitella upon illuminationof dark-treated cells, as well as in the extracellular currentpattern and pH values. A 2-min oscillation in the membrane potentialwas observed when the voltage electrode was placed close tothe border of an alkaline and acid region. Comparison of resultsfrom Chara and Nitella revealed an identical control mechanismfor external pattern stabilization in the effect of light onmembrane potential and conductance. Vibrating probe experimentsindicated that oscillations in the extracellular current occurredonly at the border of the alkaline band. Ion-specific pH micro-electrodesplaced within the alkaline band detected oscillations associatedwith light reactivation of the banding phenomenon. These resultsindicate that the oscillations represent a localized phenomenoninvolving spatially-dependent time-constants. More evidencefor the spatial dependence of time constants is gained fromsingle active acid regions in Nitella. Using this combinationof techniques, we have established that a light-dependent H⁺transporter is involved in this oscillation. Current-voltagecurves taken during these oscillations and relaxation, afterchanging the light intensity, confirmed this identification. Key words: Oscillation, vibrating probe, pH micro-electrode, time-constant. I/V curve, Chara, Nitella     

The resealing process of lipid bilayers after reversible electrical breakdown

The resealing process of lipid bilayer membranes after reversible electrical breakdown was investigated using two voltage pulses switched on together. Electrical breakdown of the membranes was induced with a voltage pulse of high intensity and short duration. The time course of the change in membrane conductance after the application of the high (short) voltage pulse was measured with a longer voltage pulse of low amplitude. The decrease in membrane conductance during the resealing process could be fitted to a single exponential curve with a time constant of 10-2 μs in the temperature range between 2 and 20°C. The activation energy for this exponential decay process was found to be about 50 kJ/mol, which might indicate a diffusion process. Above 25°C the resealing process is controlled by two exponential processes.The data obtained for the time course of the resealing process can be explained in terms of pore formation in the membranes in response to the high electrical field strength. A radius of about 4 nm is calculated for the initial pore size. From the assumed exponential change of the pore area with progressive resealing time a diffusion constant of 10^?8 cm²/s for lateral lipid diffusion can be estimated.     

Changes in Cell Length During Action Potentials in Chara

Changes in cell length during excitation in Chara were recordedsimultaneously with extracellular action potentials. Cells stimulatedin artificial pond water (APW) gave a diphasic change in celllength ; that is, a transient shortening followed by a delayedextension. When a cell was stimulated 1–3 min after aprevious shortening, the extension phase was not evident, andthe amplitude of the shortening was always larger than the previousone. Cells stimulated in moist air gave shortenings with muchlarger amplitudes and much greater durations compared with thosein APW. From such marked differences in both amplitude and durationbetween the two types of shortening it is suggested that theshortening might be caused mainly by an osmotic water movementduring excitation. Net water loss during a single action potentialwas calculated from the cell shortening to be 1.076 nl cm^–2per impulse or 59800 pmol cm^–2 per impulse, which couldbe caused by a local enhancement of ionic concentration justoutside the plasmalemma of about 0.74 mN.     

Calcium effects on electrogenic pump and passive permeability of the plasma membrane ofChara corallina

Summary Removal of Ca²⁺ from the medium results in depolarization of theChara internodal cell and an increase in membrane conductance (G _m). The increase in conductance is associated with an increase in K⁺ conductance, as judged by Ca²⁺ effects on the K⁺ dependence of clamp current. The voltage dependence ofG _m is also affected by Ca²⁺, as is the time course of the response of clamp current to a step change in voltage. Mg²⁺ restores the low conductance and the fast response to a voltage change, but not hyperpolarization at neutral pH, suggesting that there is an additional, independent effect on the electrogenic pump. The membrane does not show the normal ability to increase proton conductance at high pH in the absence of Ca²⁺; this is also restored by Mg²⁺ as well as by Ca²⁺.     

Inhibition of Cl- Channel Activation in Chara corallina Membrane by Lanthanum Ion

We examined a role of Ca²⁺ in the activation of the two majorion channels, i.e., Cl^– and K⁺ channels at the excitationof the characean plasmalemma. The current-voltage relation (I-Vcurve) of the Chara membrane was compared under the ramp voltageclamp condition before and after external application of 20µMof La³⁺ (a Ca²⁺ channel blocker). The transient inward currentcomponent, which is carried mainly by the efflux of Cl^–,disappeared almost completely in about 30 min with La³⁺ treatment.On the other hand, no effect was observed on the late largeoutward current, which is mainly carried by the efflux of K⁺in a large depolarization region (less negative than –50mV). These results suggest that the Cl^– channel in theChara plasmalemma is activated by Ca²⁺ influx, while the K⁺channel is simply activated by depolarization. (Received April 7, 1986; Accepted June 6, 1986)     

Permeability of Lipophilic Cations

The permeability (P) of a lipophilic cation, triphenylmethylphosphonium(TPMP⁺) which is frequently used as a membrane potential probe,has been measured in Chara australis (Charophyceae). P_TPMP+across biological membranes is usually thought to be very highbut this is not the case across the plasmalemma of Chara. Thepermeability of TPMP⁺ across the plasmalemma was found to betypical of inorganic cations, about 1.0 nm s^–1. Estimateswere made of the permeability of lipophilic cations across someother cell membranes, based on previously published work. Thepermeability of TPMP⁺ across the plasma membranes of the redalga, Griffithsia monilis and the blue-green alga, Anabaenavariabilis was about 2–5 nm s^–1. The permeabilityof TPMP⁺ across the plasma membranes of eukaryotes and prokaryotesappears to be similar. The permeability of lipophilic cationsacross the cristae of isolated mitochondria are exceptionallyhigh, about 170 nm s^–1. TPMP⁺ did not behave as a thiamineanalogue in Chara, unlike in the case of yeast. The means ofentry of TPMP⁺ into the Chara cell, driven by the electrochemicalgradient across the plasmalemma, has not been identified. Thepresence of a second lipophilic cation probe, DDA⁺ (dibenzyldimethylammonium),caused a decrease in the uptake flux of TPMP⁺; this suggeststhat the two lipophilic cations compete for the same site atthe surface of the plasmalemma. Key words: Chara australis, TPMP⁺, Permeability, Lipophilic cation     

The Effect of Darkness on Active and Passive Transport in Chara corallina

In Chara corallina, the membrane potential may stay much morenegative than the equilibrium potential for potassium in thedark, indicating that the proton pump is operative. The highproton conductance which occurs at high external pH, as indicatedby a high membrane conductance and a membrane potential nearthe equilibrium potential for protons, is not seen in the darkat pH 11. This effect is likely to be related to inhibitionof photosynthesis since DCMU has the same effect. The effectis similar but not identical to the effect of a decreased internalpH. Key words: Light, dark, membrane potential, Chara     

Electromotive force of Nitella membrane during excitation

Excitation of the Nitella membrane is analysed by assuming themembrane to be an electromotive force in series with a resistance,both being variables of time and of membrane potential. Duringstep depolarization beyond a threshold, conductance and electromotiveforce increase transiently, finally reaching their respectivesteady state levels. The conductance increase peak is attainedearlier than the peak for electromotive force increase. Wheneverelectromotive force increases beyond the level of clamped membranepotential, the ionic current flows inward. This is consideredto be the origin of the apparent negative resistance characteristicof the excitable membrane. Anodal break response and spontaneousfiring of Nitella membrane are also caused by transient increasesin electromotive force and conductance irrespective of whetherthe membrane potential is being held at its resting level. Thetransient increase in electromotive force reflects changes,like a phase transition, occurring during excitation. (Received May 6, 1968; )     

Electrical tolerance (breakdown) of theChara corallina plasmalemma: II. Inductive property of membrane and effects of pH o and impermeable monovalent cations on breakdown phenomenon

Summary Changes in the chord conductanceG and the membrane electromotive forceE _m in the so-called breakdown region of large negative potential of theChara plasmalemma were analyzed in more detail. In addition to the increase inG, the voltage sensitivity of the change inG increased, which was the cause of marked inductive current in the breakdown region. The breakdown potential, defined as a critical potential at which both low and high slope conductances of theI–V _m relationship cross, almost coincided with the potential at which an inductive current began to appear. This breakdown potential level changed with pH _o in a range between 5 and 9. TheChara plasmalemma was electrically most tolerant around pH _o 7.In some cellsE _m shifted to a positive level as large as +50+70 mV during the breakdown phenomenon. Such a large positive shift ofE _m is caused mainly by the increase in conductance of Cl^– and partly Ca²⁺ and K⁺.     

Effect of Sodium, Potassium, Calcium, Magnesium and Tetraethylammonium on the Transient Voltage Response to a Galvanostatic Step and of the Temperature on the Steady Membrane Conductance of Chara corallina: a Further Evidence for the Involvement of Potassium Channels in the Fast Time Variant Conductance

Homble F. 1985. Effect of sodium, potassium, calcium, magnesiumand tetraethylammonium on the transient voltage response toa galvanostatic step and of the temperature on the steady membraneconductance of Chara corallina: A further evidence for the involvementof potassium in the fast time variant conductance.—J.exp. Bot. 36: 1603–1611. Potassium channels of Chara corallina have an activation energyof 36±1 kJ mol^–1 and 50±2 kJ mol^–1at temperatures higher and lower than 15°C respectively.The fast time variant conductance property of potassium channelsis insensitive to sodium and magnesium ions and is depressedby the presence of calcium, potassium and tetraethylammoniumions. It is suggested that in Chara two different kinds of potassiumchannels exist, each kind being distinguished by their kineticsand their response to calcium and magnesium ions. Key words: —Chara corallina, membrane conductance, potassium channels, temperature     

Excitable Channels in Nitellopsis obtusa as Part of an Active Ion-Transport System

The present paper is a study on the rapid and the slow excitablechannels of Nitellopsis obtusa. The working hypothesis is thatduring the excitation of these cells a Ca²⁺-dependent activeion-transport system in the plasmalemma is activated (Gyenesand Bulychev, 1979; Gyenes, Bulychev, and Kurella, 1980) whichmay interact with a light-dependent active transport systemalso present in the plasmalemma. It is found that under conditionsof maximal light-induced current changes, registered in voltageclamp experiments, the amplitudes of both action current componentsare relatively small (10–15 µA cm²) and they increaseup to 100–150 µA cm^–2 during 15–30 minin the dark. Cells may also be excited chemically under conditionsof unchanged voltage across the plasmalemma. It is suggestedthat in the excitation process of Nitellopsis obtusa two typesof ion channels take part/emdash electrically excitable passiveand chemically excitable active channels-both incorporated inone proteolipid complex of a Ca²⁺-dependent ATPase of the plasmalemma.     

Temporal Relationship between Action Potential and Ca2+ Transient in Characean Cells

Temporal relationship between the action potential and the changein cytosolic Ca²⁺ concentration was investigated in cells offour species of Characeae, Chara corallina, Nitellopsis obtusa,Nitella flexilis and Nitella axilliformis. The Ca²⁺ transientwas detected by light emission from Ca²⁺-sensitive photoproteinaequorin injected into the cytoplasm. Action potential was triggeredby an outward or sometimes inward electric current pulse of20–50 ms in most cases. In all species the action potentialstarted at almost the same time as the time at which the lightemission from aequorin began to increase. Also the peak of actionpotential almost coincided with that of light emission, whichis in contrast with the slower Ca²⁺ transient in Chara reportedby Thiel et al. [(1997) J. Exp. Bot. 48: 609]. A discussionwas made on the origin of Ca²⁺ transient and the ionic processesduring membrane excitation. (Received July 2, 1998; Accepted October 5, 1998)