Hydrostatic pressure has a pronounced effect on the morphology and cytoskeletal organization of mammalian tissue cells. At pressures of about 300 atm (30 MPa), cells "round up"-they withdraw their lamellar extensions and greatly rearrange actin, tubulin, and several other cytoskeletal proteins. It has been proposed that these changes are caused by a pressure-induced elevation of cytosolic Ca2+ concentrations. To test this hypothesis we constructed a miniature optical pressure chamber for fluorescent light microscopy to allow measurement of cytosolic Ca2+ concentrations with the intracellular fluorescent indicator fura-2. This chamber and fura-2 were used to measure the concentrations of Ca2+ in a mouse fibroblast line (C3H 10T1/2) at pressures up to 400 atm (40 MPa). Controls included in vitro tests with standard buffers to determine the effect of pressure on fura-2 fluorescence. These controls detected a change in fura-2 fluorescence with increasing pressure, but the data indicated that pressure affects fura-2 fluorescence indirectly, by altering the pH of the solution via pressure-induced changes in the ionization of the pH buffer. These in vitro changes in fura-2 fluorescence, nevertheless, were small relative to changes in fura-2 fluorescence produced by elevation in intracellular Ca2+ concentrations in response to physiological stimulation of the cells (serum feeding after serum starvation). The mouse fibroblasts rounded at pressures of 275 atm or greater, as expected. However, no changes in cytosolic Ca2+ concentrations were detected at any pressure, at the onset of pressure, during periods of high pressure (up to 10 min), or at the release of pressure. These results strongly suggest that the mechanism by which pressure alters cell morphology and cytoskeletal organization must, at least in these cells, be something other than elevation of cytosolic Ca2+ concentrations.
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http://dx.doi.org/10.1006/excr.1996.0277 | DOI Listing |
This study characterizes a fluorescent -tdTomato neuronal reporter mouse line with strong labeling of axons throughout the optic nerve, of retinal ganglion cell (RGC) soma in the ganglion cell layer (GCL), and of RGC dendrites in the inner plexiform layer (IPL). The model facilitated assessment of RGC loss in models of degeneration and of RGC detection in mixed neural/glial cultures. The tdTomato signal showed strong overlap with >98% cells immunolabeled with RGC markers RBPMS or BRN3A, consistent with the ubiquitous presence of the vesicular glutamate transporter 2 (VGUT2, SLC17A6) in all RGC subtypes.
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Department of Physiology, University of Auckland, Auckland, New Zealand.
Contraction and relaxation within the heart is controlled by the coordinated rise and fall of Ca levels within the cytosol of cardiomyocytes. This requires Ca to be moved between subcellular and extracellular compartments with each cardiac cycle, since Ca is not destroyed or broken down by the excitation-contraction and relaxation cycles. Many cardiac pathologies alter Ca homeostasis and can lead to impaired contraction, incomplete relaxation, and arrhythmias.
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December 2024
College of Life Sciences, Beijing Normal University, Beijing, China.
Reduced nicotinamide adenine dinucleotide phosphate [NAD(P)H] oxidases (NOX) are a major cellular source of reactive oxygen species, regulating vital physiological functions, whose dys-regulation leads to a plethora of major diseases. Much effort has been made to develop varied types of NOX inhibitors, but biotechnologies for spatially and temporally controlled NOX activation, however, are not readily available. We previously found that ultraviolet A (UVA) irradiation activates NOX2 in rodent mast cells, to elicit persistent calcium spikes.
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BIOCEV, First Faculty of Medicine, Charles University, Průmyslová 595, 25250 Vestec, Czech Republic.
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