Literature DB >> 14278227

LYSOSOMAL ACID HYDROLASES IN MICE INFECTED WITH BCG.

K SAITO, E SUTER.   

Abstract

Experiments are reported dealing with the increase of lysosomal acid hydrolases induced by BCG infection. Acid hydrolases were determined quantitatively in peritoneal MP, liver homogenate, and plasma of normal and BCG-infected mice. A significant increase of acid phosphatase, beta-glucuronidase, and cathepsin was found in MP and liver homogenate of BCG-infected mice. In plasma also a significant increase of acid phosphatase and beta-glucuronidase was noticed. The results of the determination of the enzymes in centrifugally separated subcellular fractions of liver homogenate indicated clearly that the acid hydrolases associated mainly with the "large granular" fraction, which consists of mitochondria, lysosomes, and microsomes and that infection with BCG caused significant increase of the enzymes specifically in this fraction. Differences in the pattern of location among centrifugally separated fraction of liver homogenate were observed between acid phosphatase and the other two acid hydrolases. MP cultured in vitro doubled their acid phosphatases content within 24 hours, whereas beta-glucuronidase rather decreased in the same cells.

Entities:  

Keywords:  ACID PHOSPHATASE; BLOOD; BODY FLUIDS; CATHEPSIN; ENZYME TESTS; EXPERIMENTAL LAB STUDY; GLUCURONIDASE; HISTOCYTOCHEMISTRY; LIVER ENZYMOLOGY; LYSOSOMES; MICE; MICROSCOPY, ELECTRON; MYCOBACTERIUM BOVIS; PERITONEUM; PHAGOCYTOSIS; RETICULOENDOTHELIAL SYSTEM; TUBERCULOSIS IMMUNITY

Mesh:

Substances:

Year:  1965        PMID: 14278227      PMCID: PMC2137994          DOI: 10.1084/jem.121.5.727

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  17 in total

1.  THE BASIS FOR IMMUNITY TO MOUSE TYPHOID. 3. CELL-BOUND ANTIBODY.

Authors:  D ROWLEY; K J TURNER; C R JENKIN
Journal:  Aust J Exp Biol Med Sci       Date:  1964-04

2.  FACTORS AFFECTING THE LYSOSOMAL MEMBRANE AND AVAILABILITY OF ENZYMES.

Authors:  P L SAWANT; I D DESAI; A L TAPPEL
Journal:  Arch Biochem Biophys       Date:  1964-05       Impact factor: 4.013

3.  HYDROLASES OF MONONUCLEAR EXUDATE CELLS AND TUBERCULOSIS. I. EXUDATE CHARACTERISTICS, ESTERASES, PROTEINASES, AND LIPASE.

Authors:  A M DANNENBERG; W E BENNETT
Journal:  Arch Pathol       Date:  1963-11

4.  A histochemical study of acid and alkaline phosphatase in mouse livers during various conditions modifying activity of the reticuloendothelial system.

Authors:  G J THORBECKE; L J OLD; B BENACERRAF; D A CLARKE
Journal:  J Histochem Cytochem       Date:  1961-07       Impact factor: 2.479

5.  The adsorption of antigen by spleen cells previously treated with antiserum in vitro.

Authors:  S V BOYDEN; E SORKIN
Journal:  Immunology       Date:  1960-07       Impact factor: 7.397

6.  The isolation and properties of a proteolytic enzyme, cathepsin D, from bovine spleen.

Authors:  E M PRESS; R R PORTER; J CEBRA
Journal:  Biochem J       Date:  1960-03       Impact factor: 3.857

7.  Cytochemical observations on chicken monocytes macrophages and giant cells in tissue culture.

Authors:  L P WEISS; D W FAWCETT
Journal:  J Histochem Cytochem       Date:  1953-01       Impact factor: 2.479

8.  Increased activity of acid phosphatase and beta-glucuronidase in the liver and spleen of mice after intraperitoneal administration of various macromolecular substances.

Authors:  A E MEIJER; R G WILLIGHAGEN
Journal:  Biochem Pharmacol       Date:  1961-12       Impact factor: 5.858

9.  Studies on lysosomes. I. The effects of endotoxin, endotoxin tolerance, and cortisone on the release of acid hydrolases from a granular fraction of rabbit liver.

Authors:  G WEISSMANN; L THOMAS
Journal:  J Exp Med       Date:  1962-10-01       Impact factor: 14.307

10.  THE IMMUNOLOGICAL BASIS OF ACQUIRED CELLULAR RESISTANCE.

Authors:  G B MACKANESS
Journal:  J Exp Med       Date:  1964-07-01       Impact factor: 14.307

View more
  21 in total

1.  Acid phosphatase activity of virulent and avirulent clones of Leishmania donovani promastigotes.

Authors:  K Katakura; A Kobayashi
Journal:  Infect Immun       Date:  1988-11       Impact factor: 3.441

2.  Protection against dysentery infection (Shigella sonnei) by cells of peritoneal exudate, spleen, thymus, bone marrow and mesenteric lymph nodes of non-immune and specifically immunized mice.

Authors:  N B Kamzolkina
Journal:  Folia Microbiol (Praha)       Date:  1974       Impact factor: 2.099

3.  Experimental lung injury. I. Bacterial pneumonia: ultrastructural, autoradiographic and histochemical observations.

Authors:  J H Pine; W R Richter; J R Esterly
Journal:  Am J Pathol       Date:  1973-10       Impact factor: 4.307

4.  [On the formation of cytoplasmic vacuoles of leukocytes in vitro. I. Formation of cytoplasmic vacuoles in dependence on inflammatory processes (author's transl)].

Authors:  G Seebach; C Eschenbach
Journal:  Klin Wochenschr       Date:  1974-07-15

5.  Cell-mediated immunological processes in leprosy.

Authors:  J L Turk
Journal:  Bull World Health Organ       Date:  1969       Impact factor: 9.408

Review 6.  Cellular hypersensitivity and cellular immunity in the pathogensis of tuberculosis: specificity, systemic and local nature, and associated macrophage enzymes.

Authors:  A M Dannenberg
Journal:  Bacteriol Rev       Date:  1968-06

7.  Some biochemical aspects of the immune macrophage.

Authors:  G C Hard
Journal:  Br J Exp Pathol       Date:  1970-02

8.  Levels of lysosomal enzymes in tissues of mice infected with Mycoplasma fermentans.

Authors:  M G Gabridge; D M Yip; K Hedges
Journal:  Infect Immun       Date:  1975-08       Impact factor: 3.441

9.  Effects of BCG infection on the susceptibility of mouse macrophages to endotoxin.

Authors:  D L Peavy; R E Baughn; D M Musher; D M Musher
Journal:  Infect Immun       Date:  1979-04       Impact factor: 3.441

10.  Endotoxin-induced hepatic damage in BCG-infected mice.

Authors:  J W Shands; V C Senterfitt
Journal:  Am J Pathol       Date:  1972-04       Impact factor: 4.307

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.