Literature DB >> 6832824

Effect of Micropolyspora faeni cells and cell wall fractions on rabbit alveolar macrophages.

D B Learn, I S Snyder.   

Abstract

The reactivity of alveolar macrophages (AM) to cells and cell wall fractions (CWF) of Micropolyspora faeni was investigated. Exposure of cultured AM to M. faeni and its CWF caused the AM to form clumps or aggregates which remained attached to the culture dish surface. Other gram-positive and gram-negative bacteria as well as yeast, zymosan, latex microspheres, and isolated peptidoglycan from Listeria monocytogenes did not cause this response. The response was independent of species source and antibody content of the serum used in culture. The use of heat-inactivated sera negated the role of complement activation in the aggregation of AM. AM cultures required a period of culture before exposure to cells or CWF for this response to occur. This response was both time and dose dependent. Rabbit peritoneal macrophages also exhibited the clumping response. Degradation of a purified CWF, fraction 3, with lysozyme greatly diminished the clumping response. Chemical purification of fraction 3 with periodate, formamide, or trichloracetic acid also decreased this activity. These data suggest that the major active component causing this response is peptidoglycan but that other materials associated with the cell wall may also be important. A soluble-factor chemotactic for normal rabbit AM was found in the culture fluid of AM exposed to fraction 3. M. faeni cells and CWF also caused normal rabbit AM to chemiluminesce.

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Year:  1983        PMID: 6832824      PMCID: PMC348037          DOI: 10.1128/iai.39.2.948-954.1983

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  26 in total

1.  Experimental granulomatous pneumonitis: immunologic, histologic, and ultrastructural correlations.

Authors:  R E Standford; J E Salvaggio
Journal:  Chest       Date:  1976-02       Impact factor: 9.410

2.  Choline-containing teichoic acid as a structural component of pneumococcal cell wall and its role in sensitivity to lysis by an autolytic enzyme.

Authors:  J L Mosser; A Tomasz
Journal:  J Biol Chem       Date:  1970-01-25       Impact factor: 5.157

3.  Hypersensitivity pneumonitis: experimental production in guinea pigs with antigens of Micropolyspora faeni.

Authors:  B Wilkie; B Pauli; M Gygax
Journal:  Pathol Microbiol (Basel)       Date:  1973

4.  Alveolar macrophage migration inhibition in animals immunized with thermophilic actinomycete antigen.

Authors:  T Kawai; J Salvaggio; J O Harris; P Arquembourg
Journal:  Clin Exp Immunol       Date:  1973-09       Impact factor: 4.330

5.  The pathology of the acute and chronic stages of farmer's lung.

Authors:  R M Seal; E J Hapke; G O Thomas; J C Meek; M Hayes
Journal:  Thorax       Date:  1968-09       Impact factor: 9.139

6.  In vitro synthesis of factor B of the alternative pathway of complement activation by mouse peritoneal macrophages.

Authors:  C Bentley; D Bitter-Suermann; U Hadding; V Brade
Journal:  Eur J Immunol       Date:  1976-06       Impact factor: 5.532

7.  Mechanism for the inflammatory response in primate lungs. Demonstration and partial characterization of an alveolar macrophage-derived chemotactic factor with preferential activity for polymorphonuclear leukocytes.

Authors:  J A Kazmierowski; J I Gallin; H Y Reynolds
Journal:  J Clin Invest       Date:  1977-02       Impact factor: 14.808

8.  Experimental production of hypersensitivity pneumonitis with bagasse and thermophilic actinomycete antigen.

Authors:  T Kawai; J Salvaggio; W Lake; J O Harris
Journal:  J Allergy Clin Immunol       Date:  1972-11       Impact factor: 10.793

9.  A quantitative study on the activation of the alternative pathway of complement by mouldy hay dust and thermophilic actinomycetes.

Authors:  J H Edwards
Journal:  Clin Allergy       Date:  1976-01

10.  Isolation and chemical structure of the peptidoglycan of Spirillum serpens cell walls.

Authors:  P E Kolenbrander; J C Ensign
Journal:  J Bacteriol       Date:  1968-01       Impact factor: 3.490

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