Potassium-chloride promiscuous channels in mitochondrial membranes

Mitochondrial membranes isolated from a rat heart muscle were incorporated into a bilayer lipid membrane (BLM) and channel currents were measured in 250/50 mmol/l KCl cis/trans solutions. The channel currents measured from -40 to +40 mV had various linear voltage-current relationships and K(+)/Cl(-) permeability ratios at distinct voltage ranges. The channels possessed K(+)-Cl(-) promiscuous property. Depending on voltage, membrane permeability suddenly switched from K(+) over Cl(-) to Cl(-) over K(+) and back. The channels had Cl(-)/K(+) > 1 permeability at potentials around 0 mV and the permeability was switched to K(+)/Cl(-) > 1 at more negative and positive potentials. The chloride channel blocker, 5-nitro-2-(phenylpropylamino)-benzoate (NPPB, 5 x 10(-5) mol/l), influenced properties of the promiscuous channels - it activated potassium conductance of the channels.     

Ionic channels in plant cell membranes

The use of patch clamp methods for identifying ion-specific channels and other transport structures in plant cell membranes is described. Methodology, basic concepts that underlie data analysis, and applications of this powerful technique are emphasized.     

Chloride channels of intracellular membranes

Proteins implicated as intracellular chloride channels include the intracellular ClC proteins, the bestrophins, the cystic fibrosis transmembrane conductance regulator, the CLICs, and the recently described Golgi pH regulator. This paper examines current hypotheses regarding roles of intracellular chloride channels and reviews the evidence supporting a role in intracellular chloride transport for each of these proteins.     

Puroindolines form ion channels in biological membranes

Wheat seeds contain different lipid binding proteins that are low molecular mass, basic and cystine-rich proteins. Among them, the recently characterized puroindolines have been shown to inhibit the growth of fungi in vitro and to enhance the fungal resistance of plants. Experimental data, using lipid vesicles, suggest that this antimicrobial activity is related to interactions with cellular membranes, but the underlying mechanisms are still unknown. This paper shows that extracellular application of puroindolines on voltage-clamped Xenopus laevis oocytes induced membrane permeabilization. Electrophysiological experiments, on oocytes and artificial planar lipid bilayers, suggest the formation, modulated by voltage, of cation channels with the following selectivity: Cs(+) > K(+) > Na(+) > Li(+) > choline = TEA. Furthermore, this channel activity was prevented by addition of Ca(2+) ions in the medium. Puroindolines were also able to decrease the long-term oocyte viability in a voltage-dependent manner. Taken together, these results indicate that channel formation is one of the mechanisms by which puroindolines exert their antimicrobial activity. Modulation of channel formation by voltage, Ca(2+), and lipids could introduce some selectivity in the action of puroindolines on natural membranes.     

Sodium-selective channels in membranes of rat macrophages

With the use of the patch-clamp technique, highly selective nonvoltage-gated sodium channels were found in the membrane of rat peritoneal macrophages. The inward single channel currents were measured in cell-attached and outside-out mode experiments at different holding membrane potentials within the range of-60 to +40 mV. The channels had a unitary conductance of 10.2 ± 0.2 pS with 145 mm Na⁺ in the external solution at 23–24°C. The results of ion-substitution experiments confirmed that this novel type of cation channel in macrophages is characterized by high selectivity for Na⁺ over K⁺ (as for Cs⁺, NH₄ ⁺, Ca²⁺, Ba²⁺) ions, whose conduction through these sodium-permeable channels was not measurable. Lithium is the only other ion that is transported by this pathway; the unitary conductance was equal to 3.9 ± 0.2 pS in the Li⁺-containing external solution. Single channel currents and conductance were found to be linearly dependent on the external sodium concentration. Sodium channels in macrophage membrane patches were not blocked by tetrodotoxin (0.01–1 m). Single sodium currents were reversibly inhibited by the external application of amiloride (0.1–2 mm) and its derivative ethylisopropilamiloride (0.01–0.1 Mm). The mechanism of channel block by amiloride and its analogue seems to be different.We thank Dr. G.N. Mozhayeva and Dr. A.P. Naumov for useful discussions. This work has been supported by a grant from the Russian Basic Research Foundation, 93-04-21722.     

Ca-sensitive K channels in phagocytic cell membranes

In phagocytic cells evidence for properties of Ca²⁺-sensitive K⁺-selective channels comes mostly from electrophysiological studies. Macrophages and macrophage-like cells are compared with fibroblasts (L-cells) where the Ca⁺-dependent K⁺ conductance is better understood. This model shares a mesenchymal origin and an accessory phagocytic capacity with the professional phagocytes. In macrophages several values of transmembrane potentials have been measured by different groups, using various techniques. Microelectrode measurements have demonstrated a voltage-dependent K⁺ conductance involved in transition from low to high membrane potentials. Current-voltage relationships in mouse peritoneal exudate cells have revealed a region of negative slope resistance. Slow calcium spikes were found in a subpopulation of cells from human dialysis fluid that appear to be distinct from typical macrophages. Action potentials have been recorded from human monocyte-derived macrophages. Their ionic mechanism has not yet been established. Spontaneous and electrically elicited slow membrane hyperpolarizations have been described in macrophages and macrophage-like cells. Similar activity is well known in L-cells and in both cases it is possible to identify a Ca²⁺-sensitive K⁺ conductance as the underlying mechanism. Phagocytosis is a cell function that has been related to membrane hyperpolarization and to slow hyperpolarizing activity. In some cases no changes of electrical activity have been observed during the phagocytic process. Chemotactic factors induce membrane hyperpolarizations in macrophages, but the relation between electrical change and cell motility has not been established. Exocytosis, a is another Ca²⁺ sensitive cell function that awaits correlation with electrochemical changes. The evidences accumulated to date are compatible with several models for gating and modulation of the voltage-independent K⁺ conductance by Ca²⁺. The use of higher resolution techniques, such as patch-clamp, with well defined subpopulations of phagocytic cells may produce the missing link in the transduction of membrane signals into the specifically targeted cell functions.     

Nucleotide-activated chloride channels in lysosomal membranes.

Lysosomal membrane vesicles purified from rat liver contain a basal chloride conductance that was enhanced in the presence of ATP, non-hydrolysable ATP-analogs and, to a lesser extent, GTP. Other nucleotides, including AMP, ADP and cAMP, as well as CTP and UTP were not effective. Following fusion of the vesicles with an artificial phosphatidylethanolamine/phosphatidylserine bilayer, we found that ATP gamma S dramatically increased the incidence of 4,4'-diisothiocyanostilbene-2,2'-disulphonic acid (DIDS)-sensitive chloride channels with a unitary slope conductance of approx. 40 pS in 300 mM/50 mM KCl buffers and 120 pS in symmetrical 300 mM KCl buffers. Since similar results were obtained with AMP-PNP, the results indicate that lysosomes contain a chloride permeable ion channel that is activated by ATP through allosteric interaction.     

Water channels in Chara corallina

Water relations parameters ofChara corallina inter-nodes weremeasured using the single cell pressure probe. The effect ofmercurials, which are recognized as non-specific water channelinhibitors, was examined. HgCl₂ concentrations greater than5 mmol m^–3 were found to inhibit hydraulic conductivity{Lp) close to 90%, whereas pCMPS was found to have no effecton Lp. The activation energy of water flow was increased significantlyfrom 21.0 kJ mol^–1 to 45.6 kJ mol^–1, following theapplication of HgCl₂. These results are in accordance with evidencefor Hg²⁺sensitive water channels in the plasma membrane of charophytes(Henzler and Steudle, 1995; Tazawa et al., 1996). The metaboliceffects must, however, be considered in view of the rapid inhibitionof respiration and the depolarization of the membrane potentialwith HgCl₂ concentrations lower than those found to affect Lp.It was possible to measure simultaneously water relations andmembrane PD, in order to examine the contribution of potassiumchannels to Lp. Cells were induced into a K⁺ permeable state.The K⁺ channels, assumed to be open, were subsequently blockedby various blockers. No significant difference in Lp was foundfor any of these treatments. Finally, the permeability of C.corallina membranes to ethanol was examined. HgCl₂ was foundto cause a decrease in reflection coefficient, coinciding witha decrease in Lp, but there was no change in the ethanol permeabilitycoefficient. This has been interpreted in terms of both thefrictional model and composite model of non-electrolyte membranetransport. Key words: Water channels, Chara, hydraulic, conductivity, membrane transport models, reflection coefficient     

Properties of gramicidin A channels in erythrocyte membranes

Studies for the cation permeability properties of the gramicidin A channel in erythrocyte membranes are presented. It is shown that gramicidin A interacts with the membrane in a cooperative manner, creating aggregates of the antibiotic molecules in the lipid lattice of the membrane. Cationic channels exist in these aggregates with the following order of selectivity: Rb+ greater than Cs+ greater K+ greater than Na+. The cation permeability of the channels depends on the media surrounding the membrane. This finding has been explained on the basis of Hodgkin-Keynes theory for single-file ion diffusion through extra-narrow pores.     

Distribution of fertilization channels in ascidian oocyte membranes

Fertilization currents are similar in ascidian oocytes and fragments, irrespective of the size and global origin of the fragments; this result suggests that fertilization channels are distributed uniformly over the oocyte surface. Because no correlation exists between peak current and surface area of the cell, it is probable that the fertilizing spermatozoon does not open all available precursor fertilization channels, but a fixed number limited to an area around its point of entry.     

Biochemical investigations of ionic channels in excitable membranes

Summary Ion channels of excitable membranes are composed of a gating device and a selectivity filter. Two strategies are discussed in this review for the biochemical isolation and characterization of these two functional subunits of channels: Membrane molecules involved in ion translocation can be identified in vitro by their pharmacological properties, i.e. by binding assays with radioactive drugs known to selectively affect a special channel in vivo. More desirable is an assay of their true biological function, i.e. translocation of ions through a membrane. Ion flux measurements with natural and reconstituted membrane systems in vitro are recently available.This article summarizes our present knowledge of electrically excitable sodium and potassium channels of nerve membranes and of the chemically excitable sodium/potassium channel of cholinergic synapses, the acetylcholine receptor complex (AChR). Because of the availability of a great variety of drugs binding with high affinity to axonal sodium channels its investigation is more advanced than that of the axonal potassium channel. The lack of high affinity labels for the latter can be possibly overcome by photoaffinity labels which label components of the channel in situ. Initial success is reported with a photoafinity label derived from the potassium channel blocker TEA.Most advanced is the biochemical investigation of the acetylcholine receptor (AChR) which has been purified in milligram quantities. It represents a protein complex composed of different polypeptide chains with different functions regulating the sodium/potassium permeability of cholinergic postsynaptic membranes. Experiments are described to elucidate the quaternary structure, the site of binding of cholinergic ligands and neurotoxins and to prove dynamic conformation changes of the protein which may be the cause for permeability changes of the membrane. The gating device and the ion translocation system (selectivity filter, ionophor) appear to be present in the receptor complex though located possible in different subunits. This is evidenced by reconstitution of excitable membranes from purified AChR and exogenous lipids by a novel and reproducible method.An invited review article.     

Sodium-conducting channels in cardiac membranes in low calcium.

With no Ca in the patch electrode, two kinds of channels conduct Na in spontaneously beating embryonic chick heart cells. One channel conducts Na primarily during the upstroke of the action potential and is blocked by tetrodotoxin (TTX). The other channel conducts Na primarily during the late plateau and early repolarization phase of the action potential, but only in Ca concentrations below 10(-6) M. This second channel is TTX-insensitive and has a conductance of 50 to 90 pS, depending upon the interpretation of open-channel flickering. These two Na-conducting channels correspond to the channels that normally carry the fast Na current (INa) and the slow Ca current (Isi).     

Evolution of ionic channels of biological membranes

This paper presents a view of the evolution and phylogenetic distribution of ionic channels of biological membranes. The view is based on the assumptions that ionic channels (1) appeared very early in the history of life, (2) have evolved from a common ancestor, and (3) have been subjected to evolutionary pressure to reach precision and high speed of signaling. We propose that Ca2+ was the intracellular messenger and modulator of the most primitive biological systems, which implies that the first channel to appear may have been a calcium channel. Then, very soon the entire group of potassium channels evolved from the calcium channel to improve the shape of signals and to restore initial conditions. Sodium channels probably appeared relatively late, diversifying from calcium channels in the early metazoan groups. Mainly because Na+ ions do not interfere with cellular metabolism (thus allowing the inward current--and, consequently, the speed of conduction--to be greatly increased), sodium channels probably proved advantageous in the generation of the action potential, and selection replaced calcium channels with sodium channels in this function. Finally, with the acquisition of multicellularity, channels responsible for synaptic transmission appeared. The case of the acetylcholine receptor channel is briefly discussed.     

Porous membranes for reconstitution of ion channels

Functional biological synthetic composite (BSC) membranes were made using phospholipids, biological membrane proteins and permeable synthetic supports or membranes. Lipid bilayers were formed on porous polycarbonate (PC), polyethylene terephthalate (PETE) and poly (l-lactic acid) (PLLA) membranes and in 10-100 microm laser-drilled pores in a 96-well plastic plate as measured by increased resistance or decreased currents. Bilayers in 50 microm and smaller pores were stable for up to 4 h as measured by resistance changes or a current after gramicidin D reconstitution. Biological membrane transport reconstitution was then carried out. Using vesicles containing Kv1.5 K(+) channels, K(+) currents and decreased resistance were measured across bilayers in 50 microm pores in the plastic plate and PLLA membranes, respectively, which were inhibited by compound B, a Kv1.5 K(+) channel inhibitor. Functional reconstitution of Kv1.5 K(+) channels was successful. Incorporation of membrane proteins in functional form in stable permeable membrane-supported lipid bilayers is a simple technology to create BSC membranes that mimic biological function which is readily adaptable for high throughput screening.