The Effect of Calcium Ions on the Electrophysiological Properties of Single ANO6 Channels.

Proteins belonging to the anoctamin (ANO) family form calcium-activated chloride channels (CaCCs). The most unusual member of this family, ANO6 (TMEM16F), simultaneously exhibits the functions of calcium-dependent scramblase and the ion channel. ANO6 affects the plasma membrane dynamics and phosphatidylserine transport; it is also involved in programmed cell death. The properties of ANO6 channels remain the subject of debate. In this study, we investigated the effect of variations in the intracellular and extracellular concentrations of calcium ions on the electrophysiological properties of endogenous ANO6 channels by recording single ANO6 channels. It has been demonstrated that (1) a high calcium concentration in an extracellular solution increases the activity of endogenous ANO6 channels, (2) the permeability of endogenous ANO6 channels for chloride ions is independent of the extracellular concentration of calcium ions, (3) that an increase in the intracellular calcium concentration leads to the activation of endogenous ANO6 channels with double amplitude, and (4) that the kinetics of the channel depend on the plasma membrane potential rather than the intracellular concentration of calcium ions. Our findings give grounds for proposing new mechanisms for the regulation of the ANO6 channel activity by calcium ions both at the inner and outer sides of the membrane.

Calcium chelation independent effects of BAPTA on endogenous ANO6 channels in HEK293T cells.

Selective calcium chelator 1,2-Bis(2-aminophenoxy) ethane-N,N,N',N'-tetraacetic acid (BAPTA) is a common tool to investigate calcium signaling. However, BAPTA expresses various effects on intracellular calcium signaling, which are not related to its ability to bind Ca2+. In patch clamp experiments, we investigated calcium chelation independent effects of BAPTA on endogenous calcium-activated chloride channels ANO6 (TMEM16F) in HEK293T cells. We have found that application of BAPTA to intracellular solution led to two distinct effects on channels properties. On the one hand, application of BAPTA acutely reduced amplitude of endogenous ANO6 channels induced by 10 µM Ca2+ in single channel recordings. On the other hand, BAPTA application by itself induced ANO6 channel activity in the absence of the intracellular calcium elevation. Open channel probability was enhanced by increasing the intracellular BAPTA concentration from 0.1 to 1 and 10 mM. Another calcium chelator EGTA did not demonstrate chelation independent effects on the ANO6 activity in the same conditions. Due to off-target effects BAPTA should be used with caution when studying calcium-activated ANO6 channels.

Role of STIM2 and Orai proteins in regulating TRPC1 channel activity upon calcium store depletion.

Store-operated calcium channels are the major player in calcium signaling in non-excitable cells. Store-operated calcium entry is associated with the Orai, stromal interaction molecule (STIM), and transient receptor potential canonical (TRPC) protein families. Researchers have provided conflicting data about TRPC1 channel regulation by Orai and STIM. To determine how Orai and STIM influence endogenous TRPC1 pore properties and regulation, we used single channel patch-clamp recordings. Here we showed that knockout or knockdown of Orai1 or Orai3 or overexpression of the dominant-negative mutant Orai1 E106Q did not change the conductance or selectivity of single TRPC1 channels. In addition, these TRPC1 channel properties did not depend on the amount of STIM1 and STIM2 proteins. To study STIM2-mediated regulation of TRPC1 channels, we utilized partial calcium store depletion induced by application of 10 nM thapsigargin (Tg). TRPC1 activation by endogenous STIM2 was greatly decreased in acute extracellular calcium-free experiments. STIM2 overexpression increased both the basal activity and number of silent TRPC1 channels in the plasma membrane. After calcium store depletion, overexpressed STIM2 directly activated TRPC1 in the plasma membrane even without calcium entry in acute experiments. However, this effect was abrogated by co-expression with the non-permeable Orai1 E106Q mutant protein. Taken together, our single-channel patch clamp experiments clearly demonstrated that endogenous TRPC1 forms a channel pore without involving Orai proteins. Calcium entry through Orai triggered TRPC1 channel activation in the plasma membrane, while subsequent STIM2-mediated TRPC1 activity regulation was not dependent on calcium entry.

A Novel Modulator of STIM2-Dependent Store-Operated Ca2+ Channel Activity.

Store-operated Ca2+ entry is one of the main pathways of calcium influx into non-excitable cells, which entails the initiation of many intracellular processes. The endoplasmic reticulum Ca2+ sensors STIM1 and STIM2 are the key components of store-operated Ca2+ entry in mammalian cells. Under physiological conditions, STIM proteins are responsible for store-operated Ca2+ entry activation. The STIM1 and STIM2 proteins differ in their potency for activating different store-operated channels. At the moment, there are no selective modulators of the STIM protein activity. We screened a library of small molecules and found the 4-MPTC compound, which selectively inhibited STIM2-dependent store-operated Ca2+ entry (IC50 = 1 µM) and had almost no effect on the STIM1-dependent activation of store-operated channels.

Store-Operated Calcium Entry in Mouse Cardiomyocytes.

The fluorescent dye fura-2 AM was employed to record activation of Ca2+ entry in response to a decrease in Ca2+ concentration in the endoplasmic reticulum. Using whole-cell voltage clamp technique, we revealed Ca2+ currents with an amplitude of 0.46±0.13 pA/pF that passed through selective channels with current-voltage characteristics similar to those of classical store-operated CRAC channels. These currents were sensitive to 2-APB (50 µM), an inhibitor of store-operated channels. The data suggest that store-operated calcium entry is a characteristic feature of mature ventricular cardiomyocytes. Pathological alterations in store-operated Ca2+ entry can be implicated in the development of heart diseases.

Homer 1a Induces Calcium Channel Activation, but Does Not Change Their Properties in A431 Cells.

Store-operated channels activated in response to intracellular calcium store depletion represent the main pathway of calcium entry from the extracellular space in nonelectroexcitable cells. Adapter proteins organize the components of this system into integral complex. We studied the influence of adapter proteins of the Homer family on endogenous store-operated calcium Imin channels in A431 cells. Monomeric Homer 1a proteins increase activity of Imin channels, but did not modulate their electrophysiological properties. Recombinant Homer 1c protein did not block the induced calcium currents.

Huntington's Disease: Calcium Dyshomeostasis and Pathology Models.

Huntington's disease (HD) is a severe inherited neurodegenerative disorder characterized by motor dysfunction, cognitive decline, and mental impairment. At the molecular level, HD is caused by a mutation in the first exon of the gene encoding the huntingtin protein. The mutation results in an expanded polyglutamine tract at the N-terminus of the huntingtin protein, causing the neurodegenerative pathology. Calcium dyshomeostasis is believed to be one of the main causes of the disease, which underlies the great interest in the problem among experts in molecular physiology. Recent studies have focused on the development of animal and insect HD models, as well as patient-specific induced pluripotent stem cells (HD-iPSCs), to simulate the disease's progression. Despite a sesquicentennial history of HD studies, the issues of diagnosis and manifestation of the disease have remained topical. The present review addresses these issues.

Electrophysiological Features of Single Store-Operated Calcium Channels in HEK S4 Cell Line with Stable STIM1 Protein Knockdown.

An important role in intracellular calcium signaling is played by store-operated channels activated by STIM proteins, calcium sensors of the endoplasmic reticulum. In stable STIM1 knockdown HEK S4 cells, single channels activated by depletion of intracellular calcium stores were detected by cell-attached patch-clamp technique and their electrophysiological parameters were described. Comparison of the properties of single channels in HEK293 and HEK S4 cells revealed no significant differences in their current-voltage curves, while regulation of store-operated calcium channels in these cell lines depended on the level of STIM1 expression. We can conclude that electrophysiological peculiarities of store-regulated calcium entry observed in different cells can be explained by differences in STIM1 expression.

Regulation of store-operated channels by scaffold proteins in a431 cells.

Store-operated channels are major calcium influx pathways in nonexitable cells. Homer scaffold proteins are well known for their role in regulating calcium signaling. Here we report on a detailed single-channel level characterization of native store-operated channels regulated by Homer scaffold proteins in A431 carcinoma cells. By applying the single-channel patch-clamp technique, we found that different types of store-operated calcium channels have different sensitivities to Homer proteins.

[Effect of weak static magnetic fields on the excitability of a neuron].

Changes in the excitability of the neuron (amplitude, excitability threshold, rate of action potential transduction), as well as changes in the viscosity of the plasma membrane of the nerve and membranes of subcellular organelles, induced by the action of a weak magnetic field, have been studied by the methods of extracellular registration of membrane potential and combination scattering. It was found that only the threshold of excitability in intact nervous fibers increases by the action of this field. It was proven that the conformation of C40 carotenoids localized not only in plasma membranes but also in subcellular membranes of the neuron changes in a weak magnetic field. It is assumed that the changes in the excitability of the neuron by the action of weak magnetic field are due to changes in the orderliness of membrane lipids and the content of oxygen in the cytoplasm.

Image analysis of bioparticles accumulation and diamagnetic alignment in high-gradient magnetic field.

Magnetic properties of biological particles are measured in high-gradient magnetic separation (HGMS) analysis, revealing the concentrating process of nucleoprotein particles, ferritin, red blood cells, and eggs. A magnetic force acting on micrometer and submicrometer biological particles having diamagnetic or paramagnetic susceptibility with respect to the solution causes their movement and accumulation in gradient magnetic fields dependent on the values of the magnetic moments. The methods developed enable us to obtain the magnetic moments values of single particles and their assembly directly from magnetic separation and image analyses without assuming the detection of sizes. Our precision methods for the measurement of the capture traveling (magnetic diffusion) time and the accumulation (magnetic sedimentation) radius in HGMS show that it is really possible to determine the weak dia- or paramagnetic shifts of magnetic susceptibility up to 0.7x10(-10) (SI units). HGMS analysis of the concentrating process of nucleoprotein granules (microcells, DNA granules, or nucleosome core particles) with polarization microscopy reveals phase transitions for DNA in granules, and separation accumulation of particles enables the determination of the diamagnetic susceptibility and anisotropy properties. Magnetic concentration effects always occur in living systems because micrometer-located gradient magnetic fields inside an organism are strong enough to cause drifts of cellular complexes and organelles of micrometer and submicrometer sizes. We report the appearance of superparamagnetic contamination inside developing shrimp eggs. In the developing shrimps eggs, ferritin aggregates are observed under weak gradient magnetic fields and diaparaferromagnetic changes are detected. A significant interruption of egg development is revealed in such fields.

[Diagnostic and prognostic significance of study of acute phase proteins in children with appendicular peritonitis]. / Diagnosticheskoe i prognosticheskoe znachenie issledovaniia belkov ostroi fazy pri appendikuliarnom peritonite u detei.

Acute phase proteins (fibrinogen, alpha 2-macroglobulin, alpha 1-antitrypsin) were measured in 47 patients with destructive appendicitis and 203 children with local (n = 121) and disseminated (n = 82) appendicular peritonitis. The patients' ages varied from 3 to 15 years. Control group consisted of 45 age-matched children with uncomplicated umbilical and inguinal hernias. The significance of acute phase proteins in the diagnosis and preoperative and postoperative treatment planning was evaluated.

[Reversible aggregation of erythrocytes in children with appendicular peritonitis]. / Obratimaia aggregatsiia éritrotsitov pri appendikuliarnom peritonite u detei.

A microtest for quantitative evaluation of the kinetics of reversible aggregation of erythrocytes was used in 47 patients and 203 children with local (121 cases) and diffuse (82 cases) appendicular peritonitis. The patients' ages varied from 3 to 15 years. The diagnosis was confirmed clinically, intraoperatively, and morphologically during examination of removed appendices. The development of appendicular peritonitis of different dissemination was paralleled by pronounced intensification of reversible aggregation of peripheral blood erythrocytes, which suggests high diagnostic and prognostic significance of reversible aggregation of erythrocytes, determines the strategy of preoperative treatment, and helps plan the volume of intervention.

[Effect of temperature and pH on magnetic properties of human erythrocytes]. / Vliianie temperatury i pH sredy na magnitnye svoistva éritrotsitov cheloveka.

Erythrocytes magnetic susceptibility depending on temperature and pH value of buffer were studied by analysing individual erythrocytes moving in a medium in the nonhomogeneous magnetic field near a transversely magnetized thin wire.

[Energy requirements of miners engaged in open-pit coal mining]. / Energopotrebnost' gorniakov, zaniatykh dobychei uglia otkrytym sposobom.

It has been found that according to the value of daily energy consumption the coal miners engaged in open-cast mining should be referred to group III-IV of work intensity. The determining component of daily energy consumption is energy consumption during the working period the value of which depends on the character of working activity and duration of the working shift. The method of strict evaluation of the calorific value of the food taken and the control of body mass is acceptable for the assessment of daily energy consumption.

[Magnetic susceptibility and the structure of liposomes]. / Magnitnaia vospriimchivost' i struktura liposom.

Magnetic susceptibility of single liposomes sized 1-10 m was measured. Solid magnetic susceptibility of lipid-egg lecithin equalling chi et = -(5.038 +/- 0.035) X 10(-7) e.m.u./cm3 was determined. The liposome susceptibility was shown to be proportional to the number of bilayers in it and to reflect its packing.

[Theoretical estimation of the effect of magnetic fields on liposome formation]. / Teoreticheskaia otsenka vliianiia magnitnogo polia na formirovanie liposom.

In terms of equilibrium thermodynamics influence of the magnetic field on liposome formation is examined. As a result of the magnetic field influence under ultrasonic effect on water mixture of lipid structure a more homogeneous mixture must be observed due to the limits of vesicules maximum size.

[Changes in the structure of lipid bilayer membranes in magnetic fields]. / Izmeneniia v strukture bisloinykh lipidnykh membran v magnitnom pole.

In terms of structural voluminous phases the structure of bilayer lipid membranes in the constant magnetic field far from the point of phase transition is examined. The field influence on the area of the membrane black part is due to surface tension of voluminous phases. It is noted that the effect is squared with the field and is negative under gomeotropic orientation of the molecules on the surface. The dependence of the effect on temperature is predicted and its possible mechanisms are examined.

[Magnetic susceptibility and magnetic capture of cells]. / Magnitnaia vospriimchivost' i magnitnyi "zakhvat" kletok.

A phenomenon of magnetic capture of human erythrocytes and lymphocytes in paramagnetic and diamagnetic modes of motion near a transversely magnetized wire has been investigated. The values of magnetic susceptibility of numerous individual erythrocytes containing hemoglobin in various forms and lymphocytes were determined using a trajectory analysis. The distribution histograms of erythrocytes in various states and lymphocytes of magnetic susceptibility have been constructed. This histogram for lymphocytes cannot exclude magnetic identification of these cells. The method of determination of physiological concentration of methemoglobin in erythrocytes based on the distribution histogram has been suggested.