Literature DB >> 5782768

The uptake, storage, and intracellular hydrolysis of carbohydrates by macrophages.

Z A Cohn, B A Ehrenreich.   

Abstract

The exposure of cultivated mouse macrophages to sucrose (0.009-0.03 M) leads to the formation of large phase- and electron-lucent, acid phosphatase-positive vacuoles in the perinuclear region. The vacuolization process and the uptake of sucrose-(14)C is blocked by inhibitors of pinocytosis and stimulated by calf serum in the medium. These results suggest the uptake of sucrose by pinocytosis and its subsequent segregation and storage in secondary lysosomes. The addition of sucrose also increases the total content of three macrophage lysosomal hydrolases. The addition of invertase to the environment of sucrose-laden macrophages leads to the prompt shrinkage of the sucrose-containing lysosomes. This is accompanied by the intracellular hydrolysis of sucrose to fructose and glucose residues which are promptly excreted into the medium. The uptake of invertase, as indicated by the shrinkage of sucrose-containing vacuoles, is blocked by inhibitors of pinocytosis. No effect was noted when invertase was added to macrophages laden with Ficoll, a polysucrose which is not hydrolyzed by the enzyme. The influence of other carbohydrates was then investigated. Monosaccharides with molecular weights up to 220 did not produce vacuolization. However, a certain number of di-, tri-, and tetrasaccharides produced vacuolization identical with that of sucrose. Each of the disaccharides which produced vacuolization was resistant to the complement of macrophage hexosidases, whereas those that were ineffective were degraded by either macrophage or serum enzymes. The addition of beta-glucosidase to cellobiose-laden macrophages resulted in the shrinkage of vacuoles but did not alter the vacuoles of sucrose containing cells. The ability of small, neutral carbohydrates to produce lysosomal swelling is dependent upon both molecular weight and their resistance to lysosomal hydrolases.

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Year:  1969        PMID: 5782768      PMCID: PMC2138593          DOI: 10.1084/jem.129.1.201

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


  14 in total

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Authors:  D B BREWER; D HEATH
Journal:  Nature       Date:  1963-06-08       Impact factor: 49.962

2.  Pinocytosis.

Authors:  H HOLTER
Journal:  Int Rev Cytol       Date:  1959

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Authors:  D T JANIGAN; A SANTAMARIA; B F TRUMP
Journal:  J Histochem Cytochem       Date:  1960-09       Impact factor: 2.479

4.  Light and electron microscopic changes in proximal tubules of rats after administration of glucose, mannitol, sucrose, or dextran.

Authors:  A B MAUNSBACH; S C MADDEN; H LATTA
Journal:  Lab Invest       Date:  1962-06       Impact factor: 5.662

5.  The in vitro differentiation of mononuclear phagocytes. V. The formation of macrophage lysosomes.

Authors:  Z A Cohn; M E Fedorko; J G Hirsch
Journal:  J Exp Med       Date:  1966-04-01       Impact factor: 14.307

6.  The uptake and digestion of iodinated human serum albumin by macrophages in vitro.

Authors:  B A Ehrenreich; Z A Cohn
Journal:  J Exp Med       Date:  1967-11-01       Impact factor: 14.307

7.  The in vitro differentiation of mononuclear phagocytes. 3. The reversibility of granule and hydrolytic enzyme formation and the turnover of granule constituents.

Authors:  Z A Cohn; B Benson
Journal:  J Exp Med       Date:  1965-09-01       Impact factor: 14.307

8.  The isolation and selected properties of blood monocytes.

Authors:  W E Bennett; Z A Cohn
Journal:  J Exp Med       Date:  1966-01-01       Impact factor: 14.307

9.  The in vitro differentiation of mononuclear phagocytes. IV. The ultrastructure of macrophage differentiation in the peritoneal cavity and in culture.

Authors:  Z A Cohn; J G Hirsch; M E Fedorko
Journal:  J Exp Med       Date:  1966-04-01       Impact factor: 14.307

10.  The regulation of pinocytosis in mouse macrophages. II. Factors inducing vesicle formation.

Authors:  Z A Cohn; E Parks
Journal:  J Exp Med       Date:  1967-02-01       Impact factor: 14.307

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  62 in total

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Authors:  C B Saelinger; P F Bonventre; B Ivins; D Straus
Journal:  Infect Immun       Date:  1976-09       Impact factor: 3.441

2.  Cytotoxicity screening of single-walled carbon nanotubes: detection and removal of cytotoxic contaminants from carboxylated carbon nanotubes.

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3.  The breadth of macropinocytosis research.

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4.  Resistance to tumor necrosis factor-induced cell death mediated by PMCA4 deficiency.

Authors:  K Ono; X Wang; J Han
Journal:  Mol Cell Biol       Date:  2001-12       Impact factor: 4.272

5.  Passive diffusion of non-electrolytes across the lysosome membrane.

Authors:  G P Iveson; S J Bird; J B Lloyd
Journal:  Biochem J       Date:  1989-07-15       Impact factor: 3.857

6.  Normal peritoneal lymphocytes: A population with increased capacity for endocytosis.

Authors:  P J Catanzaro; R C Graham
Journal:  Am J Pathol       Date:  1974-10       Impact factor: 4.307

7.  Pinocytosis by human alveolar macrophages. Comparison of smokers and nonsmokers.

Authors:  H Yeager; S M Zimmet; S L Schwartz
Journal:  J Clin Invest       Date:  1974-08       Impact factor: 14.808

8.  A study of permeability of lysosomes to amino acids and small peptides.

Authors:  J B Lloyd
Journal:  Biochem J       Date:  1971-01       Impact factor: 3.857

9.  The effect of intralysosomal sucrose storage on the turnover of hamster fibroblast lysosomal and Golgi-apparatus enzymes.

Authors:  M J Warburton; C H Wynn
Journal:  Biochem J       Date:  1976-08-15       Impact factor: 3.857

10.  The Mikulicz cell in rhinoscleroma. Light, fluorescent and electron microscopic studies.

Authors:  E O Hoffmann; L D Loose; J C Harkin
Journal:  Am J Pathol       Date:  1973-10       Impact factor: 4.307

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