[Change in the equilibrium binding parameters of (3H)-quinuclidinylbenzilate in rabbit atrial membranes exposed to lysophosphatidylcholine].
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Animals↗
Biomedical subjects
N V Prokazova
Publications and source records attributed to N V Prokazova.
[Autoantibodies to ganglioside GM3 and serotonin in blood serum in atherosclerosis].
Using ELISA method, the sera from 17 patients with atherosclerosis and 13 normal controls were examined for ganglioside- and serotonin-reactive antibodies. Gangliosides from human liver (GM31) and human aorta (GM3a) as well as GM2, GM1, GT1b, human brain cerebrosides and the BSA-serotonin conjugate (5-HT) were used as antigens. A group of patients showed statistically significant higher levels of anti-GM31 (82%) and anti-5-HT (71%) as compared to the control group. Taking into account the identical fatty acid composition of GM3 from human liver and platelets, one can assume that antibodies are produced against blood clot gangliosides in atherosclerotic patients' sera. This conclusion is supported by a high correlation (r = 0.06, p < 0.01) between the level of antibodies to 5-HT and GM31 in the sera of all patients. The sera of three patients with the highest content of antibodies to GM31 were shown to contain antibodies to GM3a and GT1b which were absent in control sera. No reaction with brain cerebrosides or GM1 and GM2 was detected in the sera of the examined persons. The differences in sera reactions with GM31 and GM3a can be explained as resulting from differences in the chain length of fatty acid residues of the ceramide moiety of gangliosides. The data obtained confirm the fact that antibodies to aorta gangliosides appear in the sera of atherosclerotic patients. Thus, the formation of atherosclerotic plaques leading to platelet activation, clot formation and ganglioside accumulation in aortic cells increase the levels of anti-ganglioside GM3 antibodies.
Aorta↗
[Blood sialic acids in atherosclerosis].
Determination of the total (protein- and lipid-bound) sialic acid in blood sera of atherosclerotic patients (registered thickening of coronary vessels) and donors revealed that the concentration of the both types of sialic acids in the blood sera of atherosclerotic patients are increased. The concentration of total sialic acid in patients' sera was, on the average, by 20% higher than that in donors' sera. The identity of protein content in patients' and donors' sera suggests that under atherosclerosis serum proteins are sialated in a greater degree as compared to norm. The concentration of lipid-bound sialic acid in patients' sera is higher than that in donors' sera. However, calculated per blood cholesterol, the concentration of lipid-bound sialic acid is practically identical in both patient and donors, thus indicating that increased sialoglycolipid content in patients' sera correlates with increased lipoprotein content in these sera in comparison with norm.
Adult↗
Characteristics and regulation of ganglioside-induced elevation of free cytoplasmic Ca2+ in human blood platelets.
We have found that gangliosides GD3 and GM3 induced rapid, reversible elevation of free cytoplasmic Ca2+ in fura-2-loaded human blood platelets. The effect persisted in Ca(2+)-free medium, indicating that gangliosides stimulated mobilization of intracellular stores. The action of gangliosides was concentration-dependent with EC50 of about 1 microM. The Ca(2+)-mobilizing effects of gangliosides were potentiated by epinephrine and inhibited by substances inducing activation of protein kinase C and cAMP-dependent protein kinases. Acidic phospholipids partially mimicked the Ca(2+)-mobilizing effects of gangliosides indicating that lipid head charge is essential for this activity. While the elevation of [Ca2+]i produced by arachidonic acid was almost completely blocked by aspirin pretreatment, the effects of gangliosides were diminished only 2-fold, indicating that gangliosides activate both aspirin-sensitive and aspirin-insensitive mechanisms of [Ca2+]i elevation.
Arachidonic Acid↗
Neutral glycosphingolipid content and composition of cells from normal and atherosclerotic human aorta.
We have investigated the content and composition of neutral glycosphingolipids (GSLs) in the cells isolated by enzyme digestion from elastic-hyperplastic and musculo-elastic intimal layers of grossly normal and atherosclerotic regions of human aorta. We have detected three types of neutral GSLs in the intimal cells identified as glucosylceramide, trihexosylceramide and tetrahexosylceramide. We failed to detect lactosylceramide in the intimal cells. The cells of the elastic-hyperplastic layer of grossly normal regions contained trihexosylceramide and tetrahexosylceramide, while glucosylceramide was not detected. Considerable amounts of glucosylceramide were found, and the trihexosylceramide and tetrahexosylceramide content was increased in the cells isolated from atherosclerotic regions. The cells of the musculo-elastic layer of grossly normal intimal regions contained glucosylceramide, trihexosylceramide and tetrahexosylceramide. Cells of the musculo-elastic layer of the fatty streak contained noticeable higher amounts of glucosylceramide, as well as greater amounts of trihexosylceramide and tetrahexosylceramide. Cells of the musculo-elastic layer of the plaque also appeared to contain more glucosylceramide, tetrahexosylceramide, but less trihexosylceramide as compared with grossly normal regions. In both cases cells of the fatty streak exhibited the highest total amount of neutral GSLs, but at the same time the neutral GSL composition of the fatty streak was not similar to GSL composition which is known for human blood monocytes. These findings indicate that elevation of neutral GSL level is observed in cells from atherosclerotic lesions of human aortic intima.
Adult↗
Interaction of low-density lipoproteins with gangliosides.
The ganglioside uptake capacity of human serum low-density lipoproteins (LDL), the mode of ganglioside-LDL binding, and the influence of gangliosides on the floatation properties, size distribution, stability and fluorescence of LDL were investigated. The data obtained suggest that both hydrophobic and electrostatic forces are involved in formation of ganglioside-LDL complexes, but the former appear to be more important. Although association of gangliosides with LDL is predominantly unspecific, nonsaturable, and weak, a small saturable component due to specific ganglioside-apolipoprotein binding, also appears to be involved. In the presence of gangliosides the lipoprotein particles aggregate, the intrinsic fluorescence of LDL and their interaction with antibodies against apo-B change indicating that the state of apo-B [corrected] is modified by gangliosides.
Antigen-Antibody Reactions↗
Ganglioside GM3 stimulates the uptake and processing of low density lipoproteins by macrophages.
Preincubation of low density lipoproteins (LDL) with low concentrations of the ganglioside GM3 (1-2x 10(-5) M/2.5 x 10(-6) M LDL-protein) results in an increase of LDL-uptake, enhances cholesterol accumulation and cholesteryl ester formation by macrophages. At the same time the lysosomal degradation of LDL in macrophages was inhibited under these conditions. These effects depended on the ganglioside structure and concentration. It is suggested that the effects observed could be caused by GM3-induced modification of LDL to a form that becomes recognized by macrophages.
Animals↗
[Phospholipids and glycosphingolipids in cultured skin fibroblasts from healthy donors and patients with systemic scleroderma].
A comparative study of phospho- and glycosphingolipids of cultured skin fibroblast from healthy donors and from patients with systemic sclerodermia (SSD) was carried out. It was shown that the total phospholipid content in SSD fibroblasts is elevated. No significant changes in the concentration of neutral glycosphingolipids were observed. The ganglioside composition of SSD cell cultures differs significantly from that of healthy donor cells. The concentration of the gangliosides, GM3 and GM1, is decreased; no ganglioside GD1a was found in SSD fibroblasts. The data obtained are suggestive of changes in the properties of fibroblast surface which can be manifested both in the impaired reception of matrix proteins and in the impairment of basic properties of the membrane. These changes are well correlated with the results of previous studies on the AMP cyclase system.
Adult↗
Gangliosides of sea urchin embryos. Their localization and participation in early development.
The influence of antibodies to gangliosides of sea urchin Strongylocentrotus intermedius eggs on early embryos of this species was studied. gamma-Globulins were isolated from rabbit anti-ganglioside serum by micropreparative electrophoresis. These gamma-globulins produced anomalies in the development of embryos permeabilized in Triton X-100. The anomalies were not observed when anti-ganglioside gamma-globulins were added to the incubation medium together with gangliosides or when the permeabilized embryos were incubated with gamma-globulins of normal rabbit serum. Pretreatment of S. intermedius embryos with serotonin, tryptamine or some other indole derivatives led to the disappearance of ganglioside determinants from the cell surface and sharply increased immunofluorescence within the cell. Such pretreatment of embryos increased the amount of cell-associated gangliosides more than threefold as compared to untreated embryos. Serotonin was shown to bind specifically to sea urchin gangliosides immobilized on octyl-Sepharose. These observations suggest that cell-surface gangliosides, after binding drugs, are internalized and that serotonin and its antagonists inhibit the transport of newly synthesized gangliosides to the cell-surface membrane.
Animals↗
Interaction of ganglioside-containing planar bilayers with serotonin and inorganic cations.
The binding of serotonin and inorganic cations K+, Na+, Ca2+, Mg2+ to planar bilayers formed from mixtures of phosphatidylcholine and mono-, di- and trisialogangliosides was studied by the potentiodynamic and nonactin-induced potassium conductivity method. The theoretical analysis of the results obtained was made taking into account (1) protrusion of the ganglioside charges from the membrane surface and (2) simultaneous adsorption of ions on the bilayer surface and on the ganglioside charges protruding into the solution. It was shown that there was no specific binding of K+ and Na+. The binding constants for Ca2+, Mg2+ were determined. These constants for all the gangliosides studied were equal to 500 M-1. The determined binding constants of serotonin to various gangliosides diminish in the following order: GD3 greater than GT1b greater than GD1a greater than GM1.
Anti-Bacterial Agents↗
Neutral glycolipids of atherosclerotic plaques and unaffected human aorta tissue.
The composition, structure and localization of neutral glycosphingolipids of human aorta taken from subjects who had died after myocardial infarction were studied. Individual glycosphingolipids were purified by high-performance liquid chromatography and were characterized on the basis of their chromatographic mobility, carbohydrate composition, methylation analysis and by 1H-NMR spectroscopy. The main aortic glycosphingolipids were identified as glucosylceramide, lactosylceramide, globotriaosylceramide and globotetraosylceramide. Significant differences in the neutral glycosphingolipid composition of intima and media were detected. The neutral glycosphingolipid profile of medial plaques resembled that of unaffected media; however, significant differences were detected between intimal plaques and unaffected intima. Whereas the latter contained trihexosylceramide and globoside as the only neutral glycolipids, the intimal plaque glycolipids consisted mainly of glucosylceramide and also contained appreciable amounts of lactosylceramide which were completely absent in the unaffected intima. In comparison to intimal plaques, unaffected intima is characterized by a much higher content of cerebrosides terminating by beta-galactosyl residues which are known to interact with growth factors and other external stimuli. It thus seems possible that the proliferative activity of smooth muscle cells in atherosclerotic diseases is to some extent associated with their neutral glycolipid profile.
Adult↗
Ganglioside content and composition of cells from normal and atherosclerotic human aorta.
The ganglioside content and composition of cells obtained by enzyme digestion of 2 layers of human aortic intima were investigated. Five gangliosides were identified in cells isolated from the external musculo-elastic intimal layer adjacent to the media: GM3, GM1, GD3, GD1a, and GT1b. The same gangliosides plus ganglioside Gx, the chromatographic mobility of which corresponded to the mobility of ganglioside GD1b from human brain, were found in cells from the internal elastic-hyperplastic intimal layer adjacent to the vessel lumen. In both layers, the major cellular ganglioside was GM3 which represented 60% of the total cellular ganglioside content. The ganglioside content was lower in cells obtained from fatty streaks compared to cells isolated from unaffected intima. The amount of di- and trisialogangliosides in atherosclerotic plaque cells was lower, and that of monosialogangliosides higher than in cells isolated from unaffected intima. The amount of GM3 was mainly responsible for the difference in the total ganglioside content of cells obtained from different lesion types. On the whole, cells from fatty streaks contained smaller amounts of total gangliosides, whereas cells from plaques had greater total ganglioside content, than cells from unaffected intima.
Adult↗
Gangliosides influence experimental influenza virus infection in mice.
Influenza virus infection in mice may be either stimulated or partially prevented by certain gangliosides, depending on the experimental conditions employed. When injected prior to virus infection gangliosides increased the mortality rate, whereas preincubation with the virus before infection had a protecting effect. Hybrid mice resistant to influenza virus became highly susceptible to infection after injection of a specific ganglioside whereas the corresponding antiganglioside antiserum protected virus-susceptible mice against infection by the virus. These results are discussed in the light of earlier findings that various gangliosides enhance non-specific binding of influenza virus, whereas gangliosides of the GT1b and GD1b type are able to act as specific virus receptors and to promote virus penetration.
Animals↗
[Glycosylation of glycoconjugates on thymocyte surfaces].
The ectosialation and ectogalactosylation of mouse thymocyte surface were studied. The incorporation of labeled monosaccharides (N-acetylneuraminic acid and galactose) into cell surface glycoproteins and glycolipids were demonstrated. Identification of glycolipids was carried out. The effect of glycosylation on the immune properties of thymocytes was established.
Animals↗
Stimulation of platelet adhesion and activation by ganglioside GD3 adsorbed to plastic.
Platelet interaction with gangliosides GD3, GM3, GM1, GD1a and GT1b has been investigated. These gangliosides were previously identified in the vessel wall and ganglioside GD3 was found to accumulate selectively in the intima of atherosclerotic vessels. Gangliosides were adsorbed to plastic and incubated with 51Cr-labeled platelets. The adhesion of gel-filtered platelets to ganglioside GD3 was 3-4 times higher than to other immobilized gangliosides and to albumin-treated plastic. As was shown by scanning electron microscopy, GD3 stimulated intensive spreading of adherent platelets and formation of surface-bound aggregates, while only single unspread platelets were present on the surfaces coated with other gangliosides. GD3 isolated from milk and from human aorta possess the same stimulating activity. Platelet adhesion to GD3 decreased significantly in the presence of the stable prostacyclin analogue, carbacyclin.
Adsorption↗
Sialylated lactosylceramides. Possible inducers of non-specific immunosuppression and atherosclerotic lesions.
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Animals↗
The gangliosides of adult human aorta: intima, media and plaque.
The composition, structure and localization of gangliosides of aorta taken from subjects who had died after myocardial infarction were studied. Individual gangliosides were purified by high-performance liquid chromatography and high-performance thin-layer chromatography and were characterized on the basis of their chromatographic mobility, carbohydrate composition, neuraminidase hydrolysis and methylation analysis. The main aortic gangliosides were identified as GM3, GM1, GD3, GD1a and GT1b. Significant differences in the ganglioside composition of intima and media were detected and the ganglioside profile of atherosclerotic plaques was found to differ markedly from that of unaffected intima. The latter was characterized by high content of GD3, a ganglioside thought to be associated with membrane permeability, cell interaction, adhesiveness and growth and to suppress unspecific immune responses. Possible implications of the results in low-density lipoprotein binding to the arterial wall and in immunological changes induced by atherosclerotic lesions are discussed.
Adult↗
[Platelet adhesion and aggregation on a surface coated with ganglioside GD3].
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Arteriosclerosis↗