Zoltán Krasznai

Potassium channels regulate hypo-osmotic shock-induced motility of common carp (Cyprinus carpio) sperm

Abstract The osmolality and composition of fish seminal plasma usually suppress sperm motility in the testis and sperm duct. Change in the osmolality of the environment at spawning activates flagellar motion of the sperm tail. The effect of inhibitors of anion and cation channels on active motion was investigated by a microscopic motility test. While sodium channel inhibitors (amiloride and tetrodotoxin) as well as anion channel inhibitors (DIDS and ethacrynic acid) did not affect motility, potassium channel inhibitors (4-AP, quinine, veratrine, verapamil) decreased the duration of flagellar motion or abolished motility completely. Potassium channel inhibitors exerted an effect on sperm motility depending on the dose and length of incubation. The voltage-activated K+ blocker 4-aminopiridine proved to be the most potent inhibitor. Its effect was completely reversible, indicating that the functional state of potassium channels is essential to the activation mechanism of sperm. Intracellular pH of the spermatozoa was measured by a fluorescent flow cytometric technique. Hypo-osmotic shock induced intracellular alkalinization of carp sperm. Increase in pHi was 0.15 pH units. In the presence of 4-AP the measured amplitude and kinetics of the pHi change was the same as in the absence of this inhibitor, arguing against a regulatory role of intracellular pH change.

Hypo-osmotic shock induces an osmolality-dependent permeabilization and structural changes in the membrane of carp sperm

We carried out spectrofluorimetric and flow cytometric measurements to investigate the effect of hypo-osmotic shock on cell membranes of common carp sperm. The time course of the permeability of the sperm cell membrane, as monitored by DNA-related propidium iodide (PI) fluorescence, was followed for 30 min after dilution of semen in hypo-osmotic environments of different ionic strengths. Spectrofluorimetric measurements indicated a continuous increase in the total PI emission intensity of a sperm suspension. Cell-by-cell flow cytometric measurements suggested that the permeability changes were of the all-or-none type. The permeabilized fraction of cells in the individual samples was time and osmolality dependent. The number and percentage of cells in which DNA was stained by PI increased gradually over time and reached a steady-state plateau value after 5-15 min. This equilibrium fraction of cells with a PI-permeable cytoplasmic membrane displayed an inverse relationship with the osmolality of the diluent, having a near 100% value for fresh water and distilled water. Dilution of sperm in hypo-osmotic medium brought about a fast decrease in the forward light-scattering signal on a short time scale compared to the pre-steady-state time of the permeabilization. With the addition of extracellular Ca2+ (1.8 mM), restoration of the light scattering signal was observed. Permeabilization of the membrane and restoration of light scattering were not coincident in time. We propose a two-dimensional reorganization of the lipid structure as the underlying mechanism of the latter process.

Flow cytometric determination of absolute membrane potential of cells.

Membrane potential measurements using fluorescent membrane potential indicator dyes report on relative changes but usually do not result in an absolute value of the measured parameter. The method developed in this paper is based on the assumption that the negatively charged bis-oxonol distributes across the cytoplasmic membrane according to the Nernst equation. It is further supposed that the fluorescence intensity measured from a given stained cell is a single-value function of the intracellular dye concentration. The protocol suggested incorporates the construction of a calibration curve (fluorescence intensity measured from stained cells vs. extracellular dye concentration). This allows the evaluation of the membrane potential in millivolts using fluorescence readings of the cells both in the depolarized state and in the state of interest. Good agreement was found between absolute membrane potential data of human peripheral blood lymphocytes by our method and results of parallel patch clamp measurements.

Role of ion channels and membrane potential in the initiation of carp sperm motility

The exposure of freshly spawned, immotile carp sperm to hypoosmotic media triggers the initiation of calcium-dependent flagellar motility. Intracellular calcium concentration has been thought to be the critical component in motility initiation, possibly acting through a novel signalling pathway. The sensitivity of sperm cells to changes of osmolality of the environment raises the question whether a mechanoregulated osmosensitive calcium pathway is involved in the activation mechanism of carp sperm motility. The sperm cells are in a depolarized state in the seminal plasma (W = –2.6 ± 3 mV) and they hyperpolarize upon hypoosmosis-induced activation of motility (W = –29 ± 4 mV). The intracellular sodium [Na + ]i, potassium [K + ]i and calcium [Ca 2+ ]i ion concentrations were determined in quiescent cells, and at 20, 60 and 300 s after activation. The [Na + ]i and [K + ]i of the quiescent cells were similar to the [Na + ]e and [K + ]e of the seminal plasma. Following hypoosmotic shock-induced motility, both [Na + ]i and [K + ]i decreased to one-fourth of the initial concentration. The [Ca 2+ ]i doubled at initiation of the motility of the sperm cells and remained unchanged for 5 min. Bepridil (50–250 µM), a blocker of the Na + /Ca 2+ exchanger, blocked carp sperm motility reversibly. Gadolinium, a blocker of stretch-activated channels (10–20 µM), inhibited sperm motility in a dose-dependent manner and its effect was reversible. Hypoosmotic shock fluidized the membrane and gadolinium treatment made it more rigid in both quiescent cells and hypotonic shock treated but immotile sperm cells. Based on these observations, it is suggested that, besides the well-known function of potassium and calcium channels, stretch-induced conformational changes of membrane proteins are also involved in the sperm activation mechanism of common carp.

Complete inhibition of p-glycoprotein by simultaneous treatment with a distinct class of modulators and the UIC2 monoclonal antibody

P-glycoprotein (Pgp) is one of the active efflux pumps that are able to extrude a large variety of chemotherapeutic drugs from the cells, causing multidrug resistance. The conformation-sensitive UIC2 monoclonal antibody potentially inhibits Pgp-mediated substrate transport. However, this inhibition is usually partial, and its extent is variable because UIC2 binds only to 10 to 40% Pgp present in the cell membrane. The rest of the Pgp molecules become recognized by this antibody only in the presence of certain substrates or modulators, including vinblastine, cyclosporine A (CsA), and SDZ PSC 833 (valspodar). Simultaneous application of any of these modulators and UIC2, followed by the removal of the modulator, results in a completely restored steady-state accumulation of various Pgp substrates (calcein-AM, daunorubicin, and 99mTc-hexakis-2-methoxybutylisonitrile), indicating near 100% inhibition of pump activity. Remarkably, the inhibitory binding of the antibody is brought about by coincubation with concentrations of CsA or SDZ PSC 833 ∼20 times lower than what is necessary for Pgp inhibition when the modulators are applied alone. The feasibility of such a combinative treatment for in vivo multidrug resistance reversal was substantiated by the dramatic increase of daunorubicin accumulation in xenotransplanted Pgp+ tumors in response to a combined treatment with UIC2 and CsA, both administered at doses ineffective when applied alone. These observations establish the combined application of a class of modulators used at low concentrations and of the UIC2 antibody as a novel, specific, and effective way of blocking Pgp function in vivo.

Two-dimensional receptor patterns in the plasma membrane of cells. A critical evaluation of their identification, origin and information content

A concise review is presented on the nature, possible origin and functional significance of cell surface receptor patterns in the plasma membrane of lymphoid cells. A special emphasize has been laid on the available methodological approaches, their individual virtues and sources of errors. Fluorescence energy transfer is one of the oldest available means for studying non-randomized co-distribution patterns of cell surface receptors. A detailed and critical description is given on the generation of two-dimensional cell surface receptor patterns based on pair-wise energy transfer measurements. A second hierarchical-level of receptor clusters have been described by electron and scanning force microscopies after immuno-gold-labeling of distinct receptor kinds. The origin of these receptor islands at a nanometer scale and island groups at a higher hierarchical (mum) level, has been explained mostly by detergent insoluble glycolipid-enriched complexes known as rafts, or detergent insoluble glycolipids (DIGs). These rafts are the most-likely organizational forces behind at least some kind of receptor clustering [K. Simons et al., Nature 387 (1997) 569]. These models, which have great significance in trans-membrane signaling and intra-membrane and intracellular trafficking, are accentuating the necessity to revisit the Singer-Nicolson fluid mosaic membrane model and substitute the free protein diffusion with a restricted diffusion concept [S.J. Singer et al., Science 175 (1972) 720].

Temperature adaptation changes ion concentrations in spermatozoa and seminal plasma of common carp without affecting sperm motility

Abstract Cold or warm adaptation usually results in changes of the cellular parameters of poikilothermic animals. However, no data are available about the changes in cellular parameters of sperm samples from cold or warm adapted animals. Here the effects of warm and cold adaptation on the spermation of common carp ( Cyprinus carpio L.) and the changes in the characteristics of the individual sperm cells are described. Measurements were carried out on semen samples from 10 warm adapted and 10 cold adapted animals. The sperm cells from the cold adapted animals had a higher intracellular pH (7.4±0.1) than those from the warm adapted ones (7.1±0.1). The pH of the seminal plasma of the cold adapted animals (8.6±0.2) was also higher than that of the warm adapted animals (8.3±0.1). The concentration of spermatozoa in the semen of cold adapted animals was about half that for the warm adapted animals (0.7±0.1×10 10 vs. 1.4±0.2×10 10 cells/ml). The Na + concentration of the seminal plasma of the cold adapted animals (83±12 mM) was higher, while the K + concentration in these samples (64±11 mM) was lower than the corresponding data for the warm adapted animals (63±10 mM and 87±16 mM, respectively). All of these differences proved to be significant at 5% level of significance using the Students t -test. In contrast, there was no significant difference between the intracellular free K + concentrations in the spermatozoa from cold and warm adapted animals (58±8 mM vs. 60±7 mM). The ion compositions and concentrations of the blood sera of cold and warm adapted animals were similar. Also, the motile fraction and duration of motility of the spermatozoa from cold and warm adapted animals were identical. An increase by 0.2 pH unit occurred in the intracellular pH during hypoosmotic shock induced motility of sperm cells from the cold and warm adapted animals. This pH increase could be blocked by the Na + /H + exchange inhibitor amiloride in a concentration of 100 μM. Based on the kinetics of the processes involved and on additional experimental evidence it is suggested that the hypoosmotic shock induced immediate hyperpolarization of the sperm under usual spawning conditions. Thus, it may be a regulatory step in the motility activation of common carp sperm but not in the relatively slowly occurring intracellular alkalinization.

Functional consequences of Kv1.3 ion channel rearrangement into the immunological synapse.

Formation of immunological synapse (IS), the interface between T cells and antigen presenting cells, is a crucial step in T cell activation. This conjugation formation results in the rearrangement and segregation of a set of membrane bound and cytosolic proteins, including that of the T cell receptor, into membrane domains. It was showed earlier that Kv1.3, the dominant voltage-gated potassium channel of T cells redistributes into the IS on interaction with its specific APC. In the present experiments we investigated the functional consequences of the translocation of Kv1.3 channels into the IS formed between mouse helper T (T(h)2) and B cells. Biophysical characteristics of whole-cell Kv1.3 current in standalone cells (c) or ones in IS (IS) were determined using voltage-clamp configuration of standard whole-cell patch-clamp technique. Patch-clamp recordings showed that the activation of Kv1.3 current slowed (tau(a,IS)=2.36+/-0.13 ms (n=7); tau(a,c)=1.36+/-0.06 ms (n=18)) whereas the inactivation rate increased (tau(i,IS)=263+/-29 ms (n=7); tau(i,c)=365+/-27 ms (n=17)) in cells being in IS compared to the standalone cells. The equilibrium distribution between the open and the closed states of Kv1.3 (voltage-dependence of steady-state activation) was shifted toward the depolarizing potentials in T cells engaged into IS (V(1/2,IS)=-20.9+/-2 mV (n=7), V(1/2,c)=-26.4+/-1.5 mV (n=12)). Thus, segregation of Kv1.3 channels into the IS modifies the gating properties of the channels. Application of protein kinase (PK) inhibitors (PKC: GF109203X, PKA: H89, p56Lck: damnacanthal) demonstrated that increase in the inactivation rate can be explained by the dephosphorylation of the channel protein. However, the slower activation kinetics of Kv1.3 in IS is likely to be the consequence of the redistribution of the channels into distinct membrane domains.

Wide applicability of a flow cytometric assay to measure absolute membrane potentials on the millivolt scale

Abstract To prove the general applicability of a recently published flow cytometric method to determine the membrane potentials of cells on the absolute (mV) scale, the validity of the premises involved were analyzed individually. Experimental evidence was given for bis-oxonol, the applied membrane potential indicator being a Nernstian dye. The results of special measurements proved that extracellular dye concentrations were not affected by cellular dye uptake under the applied experimental conditions and that the dye content of the suspending medium did not contribute directly to the measured cellular fluorescence. A direct, membrane-potential-independent contribution of the extracellular dye to cellular fluorescence was also found to be negligible, as membrane potential values of the same type of cells evaluated from measurements in the presence of different extracellular oxonol concentrations were very close to each other. The transmembrane potential of B lymphoid JY cells was measured by the method as a function of cell density in the tissue culture. Cells isolated during the log phase of growth displayed a –40±4 mV membrane potential. At a high density of the culture (plateau phase), a significant increase of the membrane potential to –61±3 mV was observed and a medium value of –47±3.5 mV was measured at an intermediate density of the cells. Our observation indicates that nonadherent cells can also be hyperpolarized when optimal growth conditions are terminated.

Functional implications of membrane modification with semenogelins for inhibition of sperm motility in humans.

Semenogelin I and II (Sgs) are the major component of human semen coagulum. The protein is rapidly cleaved after ejaculation by a prostate-specific antigen, resulting in liquefaction of the semen coagulum and the progressive release of motile spermatozoa. Sgs inhibit human sperm motility; however, there is currently no information on its effect on the sperm membrane. This study investigated the role of Sgs on human sperm motility through regulation of membrane potential and membrane permeability. Fresh semen samples were obtained from normozoospermic volunteers, and studies were conducted using motile cells selected using the swim-up method. Sgs changed the characteristics of sperm motion from circular to straightforward as evaluated by a computer-assisted motility analyzer, and all parameters were decreased more than 2.5 mg/mL. The results demonstrate that Sgs treatment immediately hyperpolarized the membrane potential of swim-up-selected sperm, changed the membrane structure, and time-dependently increased membrane permeability, as determined through flow cytometric analysis. The biphasic effects of Sgs were time- and dose-dependent and partially reversible. In addition, a monoclonal antibody against Sgs showed positive binding to cell membrane proteins in fixed cells, observed with confocal fluorescence microscopy. These results demonstrate that Sgs modifies the membrane structure, indirectly inhibiting motility, and provides suggestions for a therapy for male infertility through selection of a functional sperm population using Sgs.