scholarly journals ACID PHOSPHATASE ACTIVITY IN INDIVIDUAL NEURONS DURING CHROMATOLYSIS: A QUANTITATIVE HISTOCHEMICAL STUDY

1970 ◽  
Vol 18 (11) ◽  
pp. 828-833 ◽  
Author(s):  
HILDE E. HIRSCH ◽  
THEODORE OBENCHAIN
Keyword(s):  
Spinal Cord ◽  
Acid Phosphatase ◽  
Phosphatase Activity ◽  
Acid Phosphatase Activity ◽  
Histochemical Study ◽  
Galactosidase Activity ◽  
Fluorogenic Substrates ◽  
Striking Increase ◽  
Staining Methods ◽  
Glucose 6 Phosphate Dehydrogenase

Two fluorogenic substrates, α-naphthyl phosphate and 4-methylumbelliferyl phosphate, were used to measure acid phosphatase activities in individual anterior horn neurons of the monkey spinal cord after section of the sciatic nerve. Although many studies utilizing staining methods have reported a striking increase in acid phosphatase activity during chromatolysis, no significant differences were observed here between the neurons of the operated and unoperated side, despite widespread chromatolysis. β-galactosidase activity was also unchanged, but the marked elevation of glucose 6-phosphate dehydrogenase during the reparative phase was confirmed.

Phosphatase Activity of Drosophila Salivary Glands

1948 ◽  
Vol s3-89 (8) ◽  
pp. 415-419
Author(s):  
W. L. DOYLE
Keyword(s):  
Acid Phosphatase ◽  
Enzymatic Activity ◽  
Quantitative Determination ◽  
Salivary Glands ◽  
Phosphatase Activity ◽  
Acid Phosphatase Activity ◽  
The State ◽  
Staining Methods

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.

Histochemical study of acid phosphatase activity in cerebral tumors

1965 ◽  
Vol 5 (1) ◽  
pp. 16-25 ◽  
Author(s):  
D. Schiffer ◽  
A. Fabiani ◽  
G. F. Monticone ◽  
G. Gabella
Keyword(s):  
Acid Phosphatase ◽  
Phosphatase Activity ◽  
Acid Phosphatase Activity ◽  
Histochemical Study ◽  
Cerebral Tumors

scholarly journals Evidence for the autophagy of microinjected proteins in HeLA cells.

1977 ◽  
Vol 75 (3) ◽  
pp. 807-817 ◽  
Author(s):  
D W Stacey ◽  
V G Allfrey
Keyword(s):  
Acid Phosphatase ◽  
Fluorescence Microscopy ◽  
Phosphatase Activity ◽  
Hela Cells ◽  
Acid Phosphatase Activity ◽  
Size Fraction ◽  
Cytoplasmic Granules ◽  
Antibody Staining ◽  
Staining Methods ◽  
High Degree

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.

Erythrophagocytosis in the Liver in Hemolytic Anemias

1968 ◽  
Vol 26 ◽  
pp. 184-185
Author(s):  
O. T. Minick ◽  
E. Orfei ◽  
F. Volini ◽  
G. Kent
Keyword(s):  
Acid Phosphatase ◽  
Oxidative Damage ◽  
Phosphatase Activity ◽  
Kupffer Cells ◽  
Acid Phosphatase Activity ◽  
Common Type ◽  
Red Cell ◽  
Cell Fragments ◽  
Reticulo Endothelial System ◽  
Important Site

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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