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Biomedical subjects

I Szász

Publications and source records attributed to I Szász.

At least 19 recordsLinked to original sources
PubMed1990

Membrane depolarization inhibits thrombin-induced calcium influx and aggregation in human platelets.

The relationship between thrombin-evoked changes in intracellular calcium concentration [( Ca2+]i) and aggregation was examined in Indo-1-loaded human platelets. The stimulus-induced intracellular calcium release and external calcium influx, as well as platelet aggregation, were studied in the same cell preparation. A close correlation between the sustained high [Ca2+]i level, depending on calcium entry, and the aggregation response was found. Gramicidin, at a concentration high enough to induce membrane depolarization, strongly inhibited the calcium influx and aggregation, but did not influence the thrombin-induced intracellular calcium release. We conclude that calcium influx through depolarization-inhibited calcium channels is a prerequisite of thrombin-induced platelet aggregation.

Blood Platelets↗
PubMed1989

Volume regulatory mechanisms of human granulocytes in hypoosmotic media.

Human neutrophil granulocytes, when placed into hypoosmotic media, first swell, than show a regulatory volume decrease (RVD) reaction. This RVD is the most effective at pH 7.5 when inosine is used as a metabolic substrate. The RVD reaction is blocked by the inhibitors of the calcium-induced K+ transport, such as quinine, quinidine, trifluoperazine (TFP), as well as by those of the conductive Cl-transport (dipyridamole, SITS, oligomycin C). Removal of external calcium by EGTA, or addition of the calcium channel inhibitor, verapamil, reduce the RVD. Ouabain affects RVD only after long preincubation and furosemide or phloretin have hardly any effect on this process. In a hypoosmotic KCl medium neutrophils show a TFP-, and SITS-sensitive secondary volume increase. All these data indicate the opening of Ca2+-induced K+ channels and of conductive Cl- channels in hypoosmotically shocked neutrophils. Under these conditions, however, direct measurement of cytoplasmic calcium by Indo-1 does not show any major change in the overall cytoplasmic free Ca2+ levels. In neutrophils, the reduced calcium signal evoked by formyl-methionyl-leucyl-phenylalanine (fMLP) after a hypoosmotic shock, suggests that cellular calcium metabolism is altered under these conditions.

Biological Transport, Active↗
PubMed1988

Volume regulatory mechanisms of human platelets.

Platelets were found to defend themselves against hypoosmotic swelling by a regulatory volume decrease mechanism, similar to that of T-lymphocytes. An oligomycin C sensitive Cl- -channel and a Ca2+-dependent, quinine- and trifluoperazine-sensitive K+-channel play a significant role in the process: platelets lose K+ and Cl- (and consequently water) through these. Activation of platelets accelerates the volume regulatory mechanism in spite of the fact that the Na+/H+ exchange process, activated simultaneously, works against volume decrease. The most rapid volume regulation was observed in activated platelets with inhibited Na+/H+ exchange process.

Blood Platelets↗
PubMed1983

Cyclic AMP-dependent protein kinase stimulates the formation of polyphosphoinositides in the plasma membranes of different blood cells.

Plasma membrane preparations from lymphocytes, platelets and red cells were phosphorylated in the presence of [gamma-32 P]ATP. The dissociated catalytic subunit of cyclic AMP-dependent protein kinase increased the 32P-labelling of proteins and polyphosphoinositides in lymphocyte, platelet and in some red cell membranes. In the majority of red cell membrane preparations the 32P-labelling of proteins and polyphosphoinositides seemed to be stimulated by the catalytic subunit of the endogenous protein kinase, since the phosphorylation was not increased by the addition of the catalytic subunit but it was decreased by the heat-stable inhibitor protein of the protein kinase. Different sets of 32P-labelled proteins were shown by SDS-gel electrophoresis in the membranes of the 3 cell types. A 24000-Mr protein was the only one which was phosphorylated by the catalytic subunit in each membrane.

Blood Platelets↗
PubMed1983

The effect of cyclic AMP-dependent protein kinase on the formation of polyphosphoinositides in erythrocyte membranes.

Inside-out vesicles from erythrocyte membrane were phosphorylated in the presence of gamma-32P-ATP. The dissociated catalytic subunit of cyclic AMP-dependent protein kinase increased the 32P-labelling of membrane proteins and polyphosphoinositides in some red blood cell membrane preparations [RBC membrane, type I] while in the majority of membrane preparations the effect of the exogeneous catalytic subunit was insignificant [RBC membrane, type II]. The phosphorylation of type II RBC membrane preparations seemed to be stimulated by the catalytic subunit of endogeneous protein kinase, since the 32P-incorporation into polyphosphoinositides and proteins was decreased by the specific heat stable inhibitor protein of the protein kinase.

Erythrocyte Membrane↗
PubMed1982

Active calcium transport and calcium-dependent membrane phosphorylation in human peripheral blood lymphocytes.

The characteristics of the calcium pump were investigated in intact human peripheral blood lymphocytes /PBL/ and in inside-out vesicles prepared from their plasma membranes. Intact PBL were loaded with calcium by a short exposure to A23187 ionophore. After the elimination of the ionophore, calcium-loaded PBL produced an ATP-dependent, external lanthanum sensitive, uphill calcium extrusion. Calcium pump in intact PBL was insensitive to ouabain and /until cellular ATP was provided/ to oligomycin and dinitrophenol. Maximum calcium extrusion rate and the alkali cation sensitivity of the process were similar to those in human red cells. Calcium was partially sequestered by PBL, and this calcium could be released by A23187 ionophore only. Inside-out plasma membrane vesicles prepared from hypotonically lysed PBL showed an ATP + Mg2+-dependent uphill calcium uptake. This calcium transport was insensitive to ouabain, oligomycin, or dinitrophenol, while blocked by lanthanum and quercetin. Calmodulin significantly stimulated calcium pumping in EDTA-washed vesicles. ATP-dependent and -independent calcium uptake rates, respectively, showed different calcium concentration dependences. When PBL membrane vesicles were phosphorylated by gamma 32P-ATP, a calcium-induced, hydroxylamine-sensitive incorporation of 32P was found in 120-150 000 molecular weight proteins. Depending on the way of membrane preparation, the molecular weight of the phosphoprotein was shifted. Similarly to that found in red cell membranes, sensitivity to calmodulin stimulation and partial proteolysis of the calcium pump molecule showed an inverse relationship.

Adenosine Triphosphate↗
PubMed1981

Ca-transport and CaMg-ATPase activity in human red cell preparations.

In intact red cells a CaMg-ATPase activity commensurable with that of the Ca-pump exists consisting mainly of protein kinase-protein phosphatase enzymes. The Ca:ATP stoichiometry of the Ca-pump is most probably 2:1, the deviation from this value at low [Ca] in inside-out-vesicles is possibly an artifact. Ca-affinity of the Ca-pump is low in intact red cells, where both calmodulin and calmodulin binding protein are present, and the cAMP-dependent activatory mechanism found in many other cells is inactive. Ca-affinity, however, can be enhanced by A23187, by Ca-EGTA buffers at the internal membrane surface (eliminating some structural divalent cations?), by enrichment in calmodulin and loss in calmodulin binding protein and by mild proteolytic effects on the inner surface of the membrane. Mild trypsin treatment of the external surface of the membrane increases the hydrolysis rate, but not the Ca-affinity of the Ca-pump and other CaMg-ATPases, increases membrane protein phosphorylation and protects against echinocytic shape transformation. All these findings reflect the interrelatedness of several membrane components influencing the rate and/or Ca-affinity of CaMg-ATPases.

Biological Transport, Active↗
PubMed1981

Erythrocyte alterations in hemoglobin H disease.

This study on erythrocytes in hemoglobin H (Hb H) disease reveals that unstable Hb H is bound to membranes to a greater extent, especially when it forms methemoglobin or is precipitated as inclusion body. The methemoglobin content of these erythrocytes is elevated in spite of a higher activity of NADH-methemoglobin reductase. The ATPase activity is doubled, and the ATP is presumably used for phosphorylation of membrane proteins, which leads to cross-linking of membrane proteins. This assumption could be supported by the observed decrease in non-electrolyte permeability, by increased binding of hemoglobin to the membrane and by polymerisation of membrane proteins detected by SDS-polyacrylamide gel electrophoresis. By means of electron microscopy, it could also be shown that the inclusion bodies are bound to the inner surface of membrane and cause its protrusion. This linkage might be responsible for the observed inhibition of the lateral movement of intramembrane particles.

Cell Membrane↗
PubMed1981

Calcium and calmodulin in the regulation of blood cell functions (a mini-review).

A great deal of cellular functions are regulated by changes in intracellular calcium concentration. Calmodulin, a low molecular weight cytoplasmic protein is basically involved in this regulation through a calcium-dependent interaction with various enzyme systems. The review discusses the chemical and physiological basis of calcium and calmodulin actions in the cell interior. Describes calcium-regulation of various functions in red cells, platelets and leukocytes.

Biological Transport↗
PubMed1980

Characteristics and regulation of active calcium transport in inside-out red cell membrane vesicles.

Sealed, inside-out human red cell membrane vesicles, prepared by a modified method of Steck (Steck T.L. (1974) in Methods in Membrane Biology (Korn, E.D., ed.), Vol 2, pp. 245-281, Plenum Press, New York), accomplish an ATP and Mg2+-dependent uphill calcium uptake with a reproducible maximum rate of 12-15 nmol/mg vesicle protein per min under physiological conditions. This maximum rate is increased by about 60-70% in the presence of a heat-stable cytoplasmic activator protein (calmodulin) obtained from red cells. Calcium efflux from inside-out vesicles is smaller than 0.01 nmol/mg vesicle protein per min at intravesicular calcium concentrations between 0.1 and 20.0 mM. In the presence of Mg2+, active calcium uptake is supported by ATP, ITP, or UTP, but not by ADP, AMP, or p-nitrophenyl phosphate. The optimum pH for the process is 7.4-7.6, and the activation energy is 19-20 kcal/mol, irrespective of the presence or absence of calmodulin. Calcium uptake in inside-out vesicles is unaffected by ouabain or oligomycin, but blocked by low concentrations of lanthanum, ruthenium red, quercetin and phloretin. K+ and Na+, when compared to choline+ or Li+, significantly increase active calcium uptake. This stimulation by K+ and Na+ is independent of that by calmodulin. Concentrated red cell cytoplasm activates calcium uptake at low soluble protein:membrane protein ratios, while a 'deactivation' of the transport occurs at high cytoplasm:membrane protein ratios. A heat-labile cytoplasmic protein fraction antagonizing calmodulin activation, can be separated by DEAE-Sephadex chromatography. Based on these findings the regulation of active calcium transport in human red cells is discussed.

Biological Transport, Active↗
PubMed1980

Effect of diaphyseal injury on the proximal growth zone of the tibia in rabbits.

In 130 growing chinchilla rabbits, the effect of various diaphyseal injuries--periosteal stripping, cortical drilling and fracture--on the growth plate and the metaphysis of the tibia was studied histologically and radiographically and with the aid of 51Cr labelled erythrocytes and the 85Sr isotope. It was found that the disturbed circulation and the venous stasis may have a marked effect on osteogenesis and bone growth but other factors are probably also involved. In the early stage after the injury an increase in the ground substance, widening of the zone of germinative and proliferative cells in the growth plate and a reticular arrangement of the bony trabeculae in the metaphysis were observed. In the late stage, along with a return to normal circulation, normalization of the osteogenesis and bone growth was also found.

Animals↗
PubMed1978

Phosphorylation of the Ca2+ pump intermediate in intact red cells, isolated membranes and inside-out vesicles.

Ca2+-entry into intact red cells containing [32P]-ATP increases the phosphorylation of the 150 000 dalton polypeptide of the membrane. This phosphorylation occurs even in Mg2+-depleted red cells. Extracellular lanthanum applied during ATP-depletion further increases the Ca2+-induced phosphorylation. In fragmented membranes or resealed insideout vesicles (IOVs) membrane bound Mg2+ is sufficient to catalyze the phosphorylation of spectrin 2 and Band 3 polypeptides with low concentrations (less than micron of [32P]-ATP. In Ca-EDTA buffers one single polypeptide is phosphorylated which is located in the 150 000 molecular weight region. KmCa for phosphorylation is much lower (0.2 micron) than for active Ca2+ transport (40 micron) in IOVs. Lanthanum induced phosphorylation (up to 250 micron Lafree) is significantly greater than Ca2+-induced phosphorylation. Hg2+ inhibits both Ca2+ and La3+ induced phosphorylation. Ca2+-induced labelling can be rapidly "chased" by unlabelled ATP+Mg2+, but not with EGTA+Mg2+. Dephosphorylation in Ca2+ phosphorylated membranes and IOVs is significantly inhibited by La3+. It can be concluded that the mechanism of La3+ and Hg2+ inhibition of the Ca2+ pump is different in intact cells and isolated membranes or Iovs.

Biological Transport, Active↗
PubMed1978

Effects of lanthanum on calcium-dependent phenomena in human red cells.

Lanthanum (0.25 mM) does not penetrate into fresh or Mg2+-depleted cells, whereas it does into ATP-depleted or ATP + 2,3-diphosphoglycerate-depleted cells, into cells containing more than 3 mM calcium, or cells stored for more than 4 weeks in acid/citrate/dextrose solution. In fresh cells loaded with calcium, extracellular lanthanum blocks the active Ca2+-efflux completely and inhibits (Ca2+ + Mg2+)-ATPase (ATP phosphohydrolase, EC 3.6.1.3) activity to about 50%. In Mg2+-depleted cells Ca2+-Ca2+ exchange is inhibited by lanthanum. Ca2+-leak is unaffected by lanthanum up to 0.25 mM concentration; higher lanthanum concentrations reduce leak rate. In NaCl medium Ca2+-leak +/ S.D. amounts to 0.28 +/ 0.08 mumol/1 of cells per min, whereas in KC1 medium to 0.15 +/ 0.04 mumol/1 of cells per min at 2.5 mM [Ca2+]e and 0.25 mM [La3+]e pH 7.1. Lanthanum inhibits Ca2+-dependent rapid K+ transport in ATP-depleted and propranolol-treated red cells, i.e. whenever intracellular calcium is below a critical level. The inhibition of the rapid K+ transport can be attributed to protein-lanthanum interactions on the cell surface, since lanthanum is effectively detached from the membrane lipids by propranolol. Lanthanum at 0.2--0.25 mM concentration has no direct effect on the morphology of red cells. The shape regeneration of Ca2+-loaded cells, however, is blocked by lanthanum owing to Ca2+-pump inhibition. Using lanthanum the transition in cell shape can be quantitatively correlated to intracellular Ca2+ concentrations.

Biological Transport, Active↗