scholarly journals LYSOSOMES IN SKELETAL MUSCLE TISSUE

1970 ◽  
Vol 45 (2) ◽  
pp. 321-333 ◽  
Author(s):  
Peter G. Canonico ◽  
John W. C. Bird
Keyword(s):  
Skeletal Muscle ◽  
Acid Phosphatase ◽  
Connective Tissue ◽  
Phosphatase Activity ◽  
Cathepsin D ◽  
Acid Phosphatase Activity ◽  
Equilibrium Density ◽  
Acid Hydrolases ◽  
Triton Wr 1339 ◽  
Arylsulfatase Activity

Postnuclear supernates from homogenates of skeletal muscle from rats subjected to starvation, injections of Triton WR-1339, dextran-500, and dextran + corticosterone were fractionated by means of rate and isopycnic zonal centrifugation in sucrose—0.02 M KCl gradients. Zonal fractions were analyzed for protein, RNA, cytochrome oxidase, and up to six acid hydrolases. The results indicate the presence of two groups of lysosome-like particles. One group contributes approximately 95% of the cathepsin D and acid phosphatase activity and 75% of the acid ribonuclease, ß-glucuronidase, and arylsulfatase activity in muscle. It is characterized by a modal equilibrium density of 1.18 that is decreased by starvation, but is not shifted by dextran-500 or Triton WR-1339. The second group has a higher proportion of acid ribonuclease, ß-glucuronidase, and arylsulftase; the equilibrium density can be shifted by dextran-500 and Triton WR-1339. It is suggested that this group of lysosomes is derived from macrophages and other connective tissue cells, whereas the former group represents lysosome-like particles from muscle cells.

Soil enzyme activities following paper sludge addition in a winter cabbage-sweet corn rotation

2000 ◽  
Vol 80 (1) ◽  
pp. 91-97 ◽  
Author(s):  
B. Gagnon ◽  
R. Lalande ◽  
R. R. Simard ◽  
M. Roy
Keyword(s):  
Alkaline Phosphatase ◽  
Acid Phosphatase ◽  
Phosphatase Activity ◽  
Acid Phosphatase Activity ◽  
Sweet Corn ◽  
Soil Enzyme ◽  
Phosphatase Activities ◽  
Arylsulfatase Activity ◽  
Papermill Sludge ◽  
Soil Acid Phosphatase

Combined primary and secondary papermill sludge (PS) is a good source of C and other nutrients for soils devoted to intensive horticultural production. A field study was conducted to evaluate the effect of PS, spring-applied alone or in combination with ammonium nitrate (AN), on the enzymatic activity of a Bedford clay (Humic Gleysol) in the province of Québec, Canada. The experiment was started in 1996 with winter cabbage (Brassica oleracea var. capitata L.) and continued in 1997 and 1998 on the same plots with sweet corn (Zea mays L.). The PS was applied at 0 (control), 8, 16, 32 and 65 Mg ha−1 in 1996 and at 44% of these rates in 1997. No sludge was applied in 1998. Additional treatments consisted of AN applied yearly at 100% of the plant N requirements and a PS and AN combination. Soil arylsulfatase and acid and alkaline phosphatase activities were measured at three different times in each growing season. The PS rate linearly increased the soil acid phosphatase activity in all 3 yr. In contrast, the alkaline phosphatase and arylsulfatase activities were enhanced in 1997 by the 8–16 Mg PS ha−1 treatments, whereas larger amounts of PS showed activity comparable to the control. The second PS application promoted phosphatase activities mostly in fall, but did not sustain arylsulfatase activity. The AN gave lower phosphatase activities than PS, and depressed arylsulfatase. Addition of AN to PS increased only acid phosphatase activity as compared with PS alone or the control. This study indicated that addition of PS improved enzyme activity of this horticultural soil but rates in excess to 32 Mg ha−1 may be detrimental. Key words: Papermill sludge, soil enzyme, cabbage, corn

Histomorphological, Histochemical and Histoenzymic Studies on the Dermis of Skin of Goat (Capra hircus)

2021 ◽  
Author(s):  
U.P. Mainde ◽  
S.B. Banubakode ◽  
N.C. Nandeshwar ◽  
R.Y. Charjan ◽  
S. Sathapathy ◽  
...  
Keyword(s):  
Acid Phosphatase ◽  
Connective Tissue ◽  
Hair Follicle ◽  
Blood Vessels ◽  
Phosphatase Activity ◽  
Acid Phosphatase Activity ◽  
Collagen Fibers ◽  
Hair Follicles ◽  
Body Regions ◽  
Root Sheath

Background: Skin is a versatile organ, which is extremely important for protection, perception, water regulation and wound healing. The skin of goat is considered extremely durable used by the tannery Industry to make rugs and carpet binding.Methods: The present study was conducted on the skin of goats of either sex to study the age wise changes in the histomorphology, histochemistry and histoenzymology of dermis. The skin samples were collected from Nagpur Muncipal Corporation Slaughter house immediately after natural death and subsequently processed and stained for histological, histochemical and histoenzymic studies. The total of 220 samples, 20 each from different body regions namely dorsal neck, lateral neck, ventral neck, dorsal thorax, lateral thorax, ventral thorax, dorsal abdomen, lateral abdomen, ventral abdomen, lateral thigh and medial thigh were collected. The animals were divided into two groups, viz. six to twelve month of age (Gr I) and above one year age (Gr II).Result: It was observed that the dermis was composed of collagen, elastic, reticular fibers, cells of connective tissue, blood vessels, nerves, hair follicles, sweat glands, sebaceous glands and arrector pili muscles in all body regions in Gr I as well as in Gr II. The dermis was divided into thin superficial papillary layer and a thick deep reticular layer. The dermal papillae were the upward projections of superficial papillary layer between epidermal pegs. In reticular layer, fibroblasts were larger, while in papillary layer, fibroblasts were thin long, compressed and spindle shaped. The collagen fibers were more in number as compared to other fibers in dermis and they were densely arranged in papillary layer and parallel with the skin surface below the epidermis. The elastic fibers were present in between the collagen fibers around the blood vessels and hair follicles. The arteriovenous shunt was found surrounded by capsule of connective tissue consisting of smooth muscle cells. The more number of hair follicles at deep part of papillary layer and few follicles were present in reticular layer. The hair follicle composed of outer root sheath, inner root sheath, cortex and medulla. The depth of primary hair follicle increased with the advancement of age. Moderate PAS positive activity was noted in the papillary layer, while it was weak to moderate in reticular layer. The reticular layer of the dermis showed moderate Sudan black B activity for the presence of lipid than the papillary layer. The mild acid phosphatase activity was seen in the papillary and reticular layer of dermis, while moderate acid phosphatase activity was noticed in the blood vessels. A mild alkaline phosphatase activity was present in dermis in Gr I and Gr II. Conclusion: The present study would form a baseline data on the histomorphology, histochemistry and histoenzymology of skin of goat which would be helpful in future research prospective.

Cell death in the ‘opaque patch’ in the central mesenchyme of the developing chick limb: a cytological, cytochemical and electron microscopic analysis

Development ◽  
1971 ◽  
Vol 26 (3) ◽  
pp. 401-424
Author(s):  
D. S. Dawd ◽  
J. R. Hinchliffe
Keyword(s):  
Cell Death ◽  
Acid Phosphatase ◽  
Phosphatase Activity ◽  
Acid Phosphatase Activity ◽  
Mesenchymal Cells ◽  
Dead Cell ◽  
Acid Hydrolases ◽  
The Dead ◽  
Secondary Lysosomes ◽  
Mesenchyme Cells

Cell death in the ‘opaque patch’ of central mesenchyme of the developing chick forelimb was investigated by a variety of light and electron-microscope cytological and cytochemical techniques. Cell death appears first at stage 23/4 (4 days) and reaches its maximum extent at stages 24 and 25 (4½ and 5 days), at which it separates the ulnar and radial mesenchymal condensations. It then decreases in size to a small area separating the proximal parts of radius and ulna and disappears at stage 28. Cytological studies show the presence of a few isolated dead cells, of mesenchymal cells containing 1–3 ingested dead cells and of macrophages containing up to 18 dead cells in various stages of digestion. These findings are interpreted as showing that isolated dead cells are ingested by neighbouring mesenchymal cells which thus become transformed into macrophages, first ingesting and then digesting further dead cells. Histochemical studies show that isolated dead cells and recently ingested dead cells contain no more acid phosphatase activity, either discrete or diffuse, than either neighbouring living mesenchymal cells, or mesenchymal cells which have ingested 1–3 dead cells. Increased acid phosphatase activity is found within the macrophages, where activity is localized within the digestive vacuoles (‘secondary lysosomes’) containing the dead cells, and within the Golgi apparatus and Golgi vesicles (‘primary lysosomes’) of macrophage cytoplasm. Loss of staining capacity by the dead cell is correlated with high acid phosphatase activity: this is interpreted as indicating the digestion of dead cells within the macrophage by acid hydrolases. There is circumstantial evidence that viable mesenchyme cells in the ‘opaque patch’ area autophagocytose part of their own cytoplasm in secondary lysosomes (1·2–2µm). The role of the ‘opaque patch’ in relation to the pattern of limb chondrogenesis is discussed. It is suggested that cell death may play a role in separation of radius and ulna, and that autophagocytosis may indicate a change in the pathway of differentiation of the mesenchyme cells lying between radius and ulna.

scholarly journals The effect of Triton WR-1339 on the subcellular distribution of Trypan Blue and 125I-labelled albumin in rat liver

1973 ◽  
Vol 136 (1) ◽  
pp. 57-65 ◽  
Author(s):  
Malcolm Davies
Keyword(s):  
Acid Phosphatase ◽  
Density Gradient ◽  
Cathepsin D ◽  
Trypan Blue ◽  
Gradient Centrifugation ◽  
Distribution Patterns ◽  
Equilibrium Density ◽  
Sucrose Density Gradient Centrifugation ◽  
Ionic Detergent ◽  
Triton Wr 1339

1. The density-gradient distribution patterns of acid phosphatase, Trypan Blue and denatured 125I-labelled albumin were studied by discontinuous sucrose- and isopycnic sucrose-density-gradient centrifugation on combined heavy and light mitochondrial (M+L) fractions of liver isolated from normal rats and from rats injected with Triton WR-1339. 2. The results obtained from the subfractionation of the M+L pellet of normal animals indicate that the equilibrium density of Trypan Blue and acid-insoluble radioactivity is the same as that for acid phosphatase, which suggests they are bound by a common membrane to form a distinct subcellular population of lysosomal nature. 3. In contrast, the analysis of the isopycnic gradients obtained on subfractionation of M+L pellets of liver isolated from rats treated with Triton WR-1339 show that the acid-insoluble radioactivity has an equilibrium density around 1.21, whereas the acid hydrolases, including cathepsin D, show the characteristic shift to an equilibrium density of around 1.12. Trypan Blue is distributed along the gradient with distinct peaks at densities 1.22 and 1.12. 4. Similar equilibrium-density distribution patterns were obtained with M+L pellets isolated from rats pretreated with Triton WR-1339 but not injected with Trypan Blue. 5. Treatment of the rats with Triton WR-1339 does not affect albumin digestion of isolated intact lysosomes despite the fact that most of the cathepsin D and the albumin ingested by phagocytosis are located in different vacuoles. 6. It is concluded from these experiments that in the liver of animals treated with Triton WR-1339 125I-labelled albumin is located within heterophagosomes which do not fuse with heterolysosomes containing the non-ionic detergent Triton WR-1339. The inability of these two lysosomal populations to fuse is not due to Trypan Blue.

scholarly journals Studies on bone enzymes. The assay of acid hydrolases and other enzymes in bone tissue

1965 ◽  
Vol 97 (2) ◽  
pp. 380-388 ◽  
Author(s):  
G Vaes ◽  
P Jacques
Keyword(s):  
Acid Phosphatase ◽  
Cytochrome Oxidase ◽  
Phosphatase Activity ◽  
Acid Phosphatase Activity ◽  
Acid Hydrolases ◽  
Newborn Rat ◽  
Optimum Activity ◽  
Chemical Agents ◽  
Acid Deoxyribonuclease ◽  
Beta Galactosidase

1. Nine acid hydrolases, cytochrome oxidase, alkaline phenylphosphatase and catalase were demonstrated in 0.25m-sucrose homogenates of newborn-rat calvaria. The acid hydrolases were: acid phenylphosphatase, acid beta-glycerophosphatase, beta-glucuronidase, beta-N-acetylglucosaminidase (beta-N-acetylaminodeoxyglucosidase), acid ribonuclease and acid deoxyribonuclease, showing optimum activity at about pH5; cathepsin, beta-galactosidase and hyaluronidase, with optimum activity at about pH3.6. 2. The main kinetic characters of these enzymes have been studied and methods for their quantitative assay have been worked out. The activities present in bone are given and compared with those found in liver. 3. Acid-phosphatase activity was assayed with phenyl phosphate and beta-glycerophosphate as substrates: activities with these two substrates appeared to be due to two different enzymes. Acid phenylphosphatase is particularly labile and is readily inactivated by various physical or chemical agents.

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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