scholarly journals CORRELATION OF ACID PHOSPHATASE ACTIVITY WITH DEGREE OF BACTERIAL INFECTION IN HELA CELLS

1966 ◽  
Vol 14 (2) ◽  
pp. 196-202 ◽  
Author(s):  
HELEN ROLAND JERVIS ◽  
EUGENE H. LABREC

Acid phosphatase activity has been demonstrated in HeLa cells grown in monolayers on coverslips, using the histochemical method of Barka and Anderson. In normal interphase cells variable enzymatic activity may always be demonstrated in a juxtanuclear position. When the culture medium is inoculated with a virulent strain of Shigella flexneri 2a, a certain number of cells in invaded by the organisms. In the presence of one organism, the acid phosphatase activity of the infected cell appears to increase, but as more organisms are found in individual cells, the intensity of the cells enzymatic reaction decreases. Biochemical assays on whole cell monolayers to quantitate this decrease have failed to show a significant change in enzymatic activity between infected and control cultures, possibly due to the high percentage of cells in any culture that were not infected or infected only slightly.

1948 ◽  
Vol s3-89 (8) ◽  
pp. 415-419
Author(s):  
W. L. DOYLE

The phosphatases in the cytoplasm and nuclei of Drosophila salivary glands are better preserved by fixation in absolute acetone than in 85 per cent, alcohol. In whole glands there is relatively little extraction of the enzyme during assay. Phosphatase activity is more resistant to incubation at neutrality than at pH 8.6, but in this material there is sufficient residual enzymatic activity to permit redetermination of alkaline, neutral, or acid phosphatase activity by staining methods after an initial quantitative determination. The state of the membranes of the gland affects the penetration of the substrate sufficiently to limit the activities obtained.


2020 ◽  
Vol 66 (No. 2) ◽  
pp. 93-98
Author(s):  
Beata Kuziemska ◽  
Andrzej Wysokiński ◽  
Joanna Trębicka

A three-year pot experiment carried out in the vegetation hall in 2014–2016 included studying the enzymatic activity of soil, into which various amounts of copper: (100, 200 and 300 mg Cu/kg soil) and organic materials (cattle manure, chicken manure, post-mushroom substrate) were introduced, used separately, at a soil-introduction dose of 2 g C<sub>org</sub>/kg. Copper and organic materials were used once, only in the first year of the study, before sowing test plant orchard grass. In soil collected after the last (fourth) swath of grass in each year of the study, the activity of urease, dehydrogenases, acid, and alkaline phosphatase was determined. Applications of copper to the soil, regardless of its dose, resulted in a decrease in urease, dehydrogenases and alkaline phosphatase and an increase in acid phosphatase activity. The inactivating effect of this metal on the activity of urease, dehydrogenases and alkaline phosphatase increased with the increase of its dose. Organic fertilisation generally increased the enzymatic activity of the analysed soil. In subsequent years of the study, urease and alkaline phosphatase activity decreased, while acid phosphatase activity increased. Dehydrogenase activity did not change significantly in subsequent years of the study.  


2004 ◽  
Vol 64 (4) ◽  
pp. 853-858 ◽  
Author(s):  
M. Porawski ◽  
G. F. Wassermann ◽  
M. Achaval

Acid phosphatase (AcP) activity was investigated in the testes of two species of teleosts in two seasons: summer and winter. AcP activity was detected in Sertoli cells from tilapia (Oreochromis niloticus) only during the nonreproductive period of its annual cycle, corresponding to the winter months. In kingfish (Odonthestes perugiae), the enzymatic reaction was identified during the non-reproductive period (summer) in epithelial cells of the efferent ducts but not in Sertoli cells. These data suggest that the enzyme is involved in the absorption of residual spermatid cytoplasm and as well as in the removal of spermatozoa remaining after the reproductive period. In kingfish, this heterophagous function is carried out by the efferent duct cells and not by Sertoli cells.


1969 ◽  
Vol 20 (1) ◽  
pp. 99 ◽  
Author(s):  
BA Panaretto ◽  
KA Ferguson

Newly shorn sheep were exposed to a cold (3°C) wet environment for 8 days; six out of 10 untreated animals died but there were no deaths in a group of 10 that was treated with cortisone. In two other experiments, nine out of 15 control sheep died, but only four out of 15 sheep treated with adrenocorticotrophin (ACTH). In a final experiment approximately one-third of exposed controls died compared with one-tenth of sheep treated with dexamethasone trimethylacetate. A significantly greater proportion (P < 0.05) of sheep given ACTH or 1.5 mg or more of dexamethasone trimethylacetate per kg had rectal temperatures higher than 37.8°C during the first 96 hr of exposure than the comparable controls. The adrenal glands of sheep that died in the cortisone and ACTH experiments were heavier than those taken from survivors that were killed after the experiment; macroscopically, the cortices of some of the adrenals from sheep that succumbed were haemorrhagic and resembled the glands seen in the Waterhouse-Friderichsen syndrome in man; all were heavily infiltrated with lipid when compared with the cortices of survivors. ß-Glucuronidase activity in the serum of cortisone-treated sheep (and in untreated survivors) was elevated during the first 2–3 days of exposure and returned to pre-exposure levels; untreated sheep that succumbed showed continuously increasing enzymatic activity. Acid phosphatase activity was initially depressed in steroid-treated sheep and returned to pre-exposure levels, whereas activity increased continuously in controls that died. Total leucocytes were lower during the first 72 hr of exposure in sheep treated with 1.5–2 mg dexamethasone trimethylacetate per kg, compared with untreated controls. We suggest that the enlarged, fat-laden haemorrhagic adrenals found in sheep that died from cold exposure resulted from excessive ACTH stimulation prior to death. The results suggested a state of adrenocortical insufficiency during the first 96 hr of cold exposure.


1968 ◽  
Vol 16 (3) ◽  
pp. 199-204 ◽  
Author(s):  
H. DARIUSH FAHIMI ◽  
PIERRE DROCHMANS ◽  
A. POPOWSKI

The inhibition of acid phosphatase activity in rat liver homogenates after fixation in different lots of commercial glutaraldehyde is determined and compared with the inhibition following fixation with a distilled product. It is shown that commercial glutaraldehydes inhibit more of the enzyme activity than the distilled product. The acidic products of oxidation of glutaraldehyde do not increase the inhibition of the enzymatic activity. The presence of high concentration of inorganic phosphates in different lots of commercial glutaraldehyde, as presented here, suggests that probably such impurities may be responsible for increased inhibition of phosphatase activity noted after fixation in commercial glutaraldehydes.


2014 ◽  
Vol 61 (2) ◽  
pp. 253-264 ◽  
Author(s):  
Barbara Kieliszewska-Rokicka

Mycorrhizal and control seedlings of Scots pine (<i>Pinus sylvestris</i> L.) were grown under axenic conditions at various concentrations of nitrogen (0.17 mM, 3.78 mM, 18.92 mM) and phosphorus (0.25 mM, 5.58 mM, 23.5 mM). Enzyme activities of soluble acid phosphatase of excised roots (surface-accessible activity) and of crude enzyme preparations of root tissue (total soluble activity) were analyzed in control and mycorrhizal seedlings. The content of P in pine shoot was also measured. The intermediate supply of nitrogen and phosphorus (N = 3.78 mM, P= 5.58 mM) was optimal for development of ectomycorrhizae. Activity of acid phosphatase was stimulated by higher levels of N in the soil and was higher in mycorrhizal than non-mycorrhizal roots. Pine roots had greater acid phosphatase activity at the reduced than at the higher P concentrations. The presence of mycorrhizae increased the activities of both surface-accessible and total soluble enzyme activities at lower P supply (0.25 mM, 5.58 mM) and decreased it significantly at the highest P concentration (23.5 mM). P content in shoots was higher in mycorrhizal than non-mycorrhizal seedlings.


1977 ◽  
Vol 75 (3) ◽  
pp. 807-817 ◽  
Author(s):  
D W Stacey ◽  
V G Allfrey

Rhodamine-conjugated proteins were microinjected into living HeLa cells. Fluorescence microscopy was then employed to study their segregation from the cytoplasm into lysosomes. Results obtained in this way were verified when the corresponding unconjugated proteins were localized by autoradiographic, histological, and antibody-staining methods after their microinjection. Most injected proteins were segregated into cytoplasmic granular structures during their removal from cells. As evidence that these were autophagic vacuoles, they were found to contain no detectable acid phosphatase activity upon formation, after which they moved to the juxtanuclear position of lysosomes and appeared to fuse with them. The segregation of microinjected proteins exhibited a high degree of selectivity. The half-times of placement of individual exogenous proteins into cytoplasmic granules varied from 3 h to nearly 3 days, and one protein, hemoglobin, was never observed to enter them. Furthermore, endogenous HeLa proteins in a size fraction near 200,000 daltons were segregated much more rapidly than those in a fraction near 40,000 daltons. In these studies, rapid protein segregation appeared to take place by a mechanism of exclusion of the injected protein from numerous cytoplasmic domains.


1960 ◽  
Vol 7 (2) ◽  
pp. 329-334 ◽  
Author(s):  
Edward Essner

The present study describes a submicroscopic surface fragmentation of erythrocytes which occurs in the ascitic fluid of rats bearing the Novikoff ascites hepatoma. The resulting fragments attach to the surface of macrophages and are phagocytized by pseudopod formation. Plasma membrane in the region of these phagocytosis vacuoles appears to condense into electron-opaque material, suggesting an alteration in its physicochemical state. Stages in intracellular digestion of intact erythrocytes or small fragments within the phagocytosis vacuoles are illustrated; no particles resembling ferritin are observed. The phagocytosis vacuoles possess high levels of acid phosphatase activity. They may be called phagosomes, a type of lysosome. There is no indication of a connection between phagosomes and other formed cytoplasmic organelles. Small vacuoles of the order of 80 mµ in diameter, which may represent pinocytosis vacuoles, are present in the cytoplasm and some appear to be in contact with the phagosome membrane, reminiscent of observations of Rose with HeLa cells.


Author(s):  
O. T. Minick ◽  
E. Orfei ◽  
F. Volini ◽  
G. Kent

Hemolytic anemias were produced in rats by administering phenylhydrazine or anti-erythrocytic (rooster) serum, the latter having agglutinin and hemolysin titers exceeding 1:1000.Following administration of phenylhydrazine, the erythrocytes undergo oxidative damage and are removed from the circulation by the cells of the reticulo-endothelial system, predominantly by the spleen. With increasing dosage or if animals are splenectomized, the Kupffer cells become an important site of sequestration and are greatly hypertrophied. Whole red cells are the most common type engulfed; they are broken down in digestive vacuoles, as shown by the presence of acid phosphatase activity (Fig. 1). Heinz body material and membranes persist longer than native hemoglobin. With larger doses of phenylhydrazine, erythrocytes undergo intravascular fragmentation, and the particles phagocytized are now mainly red cell fragments of varying sizes (Fig. 2).


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