46 research outputs found
Development of a delayed outward-rectifying K+ conductance in cultured mouse peritoneal macrophages.
Hysteresis and bi-stability by an interplay of calcium oscillations and action potential firing
Many cell types exhibit oscillatory activity, such as repetitive action
potential firing due to the Hodgkin-Huxley dynamics of ion channels in the cell
membrane or reveal intracellular inositol triphosphate (IP) mediated
calcium oscillations (CaOs) by calcium-induced calcium release channels
(IP-receptor) in the membrane of the endoplasmic reticulum (ER). The
dynamics of the excitable membrane and that of the IP-mediated CaOs have
been the subject of many studies. However, the interaction between the
excitable cell membrane and IP-mediated CaOs, which are coupled by
cytosolic calcium which affects the dynamics of both, has not been studied.
This study for the first time applied stability analysis to investigate the
dynamic behavior of a model, which includes both an excitable membrane and an
intracellular IP-mediated calcium oscillator. Taking the IP
concentration as a control parameter, the model exhibits a novel rich spectrum
of stable and unstable states with hysteresis. The four stable states of the
model correspond in detail to previously reported growth-state dependent states
of the membrane potential of normal rat kidney fibroblasts in cell culture. The
hysteresis is most pronounced for experimentally observed parameter values of
the model, suggesting a functional importance of hysteresis. This study shows
that the four growth-dependent cell states may not reflect the behavior of
cells that have differentiated into different cell types with different
properties, but simply reflect four different states of a single cell type,
that is characterized by a single model.Comment: 29 pages, 6 figure
Whole-Cell K+ Currents across the Plasma Membrane of Tobacco Protoplasts from Cell-Suspension Cultures
Novel Approaches to Treat Experimental Pulmonary Arterial Hypertension: A Review
Background. Pulmonary arterial hypertension (PAH) is a life-threatening disease characterized by an increase in pulmonary artery pressure leading to right ventricular (RV) hypertrophy, RV failure, and ultimately death. Current treatments can improve symptoms and reduce severity of the hemodynamic disorder but gradual deterioration in their condition often necessitates a lung transplant. Methods and Results. In experimental models of PAH, particularly the model of monocrotaline-induced pulmonary hypertension, efficacious treatment options tested so far include a spectrum of pharmacologic agents with actions such as anti-mitogenic, proendothelial function, proangiogenic, antiinflammatory and antioxidative. Emerging trends in PAH treatment are gene and cell therapy and their combination, like (progenitor) cells enriched with eNOS or VEGF gene. More animal data should be collected to investigate optimal cell type, in vitro cell transduction, route of administration, and number of cells to inject. Several recently discovered and experimentally tested interventions bear potential for therapeutic purposes in humans or have been shown already to be effective in PAH patients leading to improved life expectation and better quality of life. Conclusion. Since many patients remain symptomatic despite therapy, we should encourage research in animal models of PAH and implement promising treatments in homogeneous groups of PAH patients
Analysis of decaying unitary currents in on-cell patches of cells with a high membrane resistance
Under nonideal voltage-clamp conditions, unitary currents in the cell- attached patch (CAP) configuration of the patch-clamp technique are decaying instead of rectangular. From these data, four parameters can be determined when multiple identical channels are present. We analyzed an electrical equivalent circuit of the CAP configuration. This analysis yielded, for single-channel resistance, attached-cell membrane resistance, patch resistance, and attached-cell membrane capacitance, a set of different equations to calculate their values from these four parameters. To choose the most robust equation, those that yielded the same resistor/capacitance were compared on the basis of their sensitivity for inevitable deviations of the parameters from their nominal values. The results of our theoretical study are of methodological interest: 1) because they confirm that, under special conditions, CAP measurements can be used to measure electrical membrane properties of intact cells (this is important inasmuch as the CAP is the only configuration in which the cytoplasm of cells remains undisturbed) and 2) because we identify the level of voltage clamp and the equations with which the electrical properties can be determined with optimal accuracy
Voltage-activated K+ conductances in freshly isolated embryonic chicken osteoclasts
Patch-clamp measurements on freshly isolated embryonic chicken osteoclasts revealed three distinct types of voltage-dependent K+ conductance. The first type of conductance, present in 72% of the cells, activated at membrane potentials less negative than -30 to -20 mV and reached full activation at +40 mV. It activated with a delay, reached a peak value, and then inactivated with a time constant of approximately 1.5 s. Inactivation was complete or almost so. Recovery from inactivation, at -70 mV, had a time constant of roughly 1 s. The conductance could be blocked, at least partly, by 4 mM 4-aminopyridine. The second type of conductance (present in all cells) activated at membrane potentials more negative than -40 to -80 mV and reached full activation at -130 mV. Activation potential and maximal conductance were dependent on the extracellular K+ concentration. Inactivation of the conductance first became apparent at membrane potentials more negative than -100 mV and was a two-exponential process. The conductance could be blocked by external 5 mM Cs+ ions. The third type of conductance (present in all cells) activated at membrane potentials more positive than +30 mV. Generally, the conductance did not inactivat