Literature DB >> 5807279

The chemical nature of macrophage RNA-antigen complexes and their relevance to immune induction.

G E Roelants, J W Goodman.   

Abstract

10 different compounds, including natural and synthetic polypeptides, proteins, polysaccharides, amino acids, and steroid hormones, were assayed for their capacity to form complexes with peritoneal exudate cell RNA. Only molecules carrying negatively charged groups were able to do so. The formation of RNA-antigen complexes was unrelated to the immuno-potency of the "antigen," was not an enzyme-dependent reaction, did not require the synthesis of RNA following introduction of the antigen, did not seem to involve antigen-specific RNAs, was not specific for macrophages, since HeLa cells could be used as effectively, and occurred when purified RNA was mixed with antigen only in the presence of divalent cations. The complexes were very stable, once formed, but could be dissociated by exhaustive dialysis against buffers containing a chelating agent. The macrophage RNA-antigen complex therefore appears to be a chelate between anionic groups on the two components. Based on the total absence of a relationship between immunogenicity and the capacity to form such complexes, as well as the nonspecific nature of complex formation at every level examined, it appears unlikely that RNA-antigen complexes play a physiologically significant role in immune induction.

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Year:  1969        PMID: 5807279      PMCID: PMC2138705          DOI: 10.1084/jem.130.3.557

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


  36 in total

1.  Immunochemical studies on the poly-gamma-D-glutamyl capsule of Bacillus anthracis. I. Characterization of the polypeptide and of the specificity of its reaction with rabbit antisera.

Authors:  J W Goodman; D E Nitecki
Journal:  Biochemistry       Date:  1966-02       Impact factor: 3.162

2.  The effect of environment on the structure and helix-coil transition of soluble ribonucleic acid.

Authors:  D B Millar; R F Steiner
Journal:  Biochemistry       Date:  1966-07       Impact factor: 3.162

3.  Renaturation of transfer ribonucleic acids through site binding of magnesium.

Authors:  T Lindahl; A Adams; J R Fresco
Journal:  Proc Natl Acad Sci U S A       Date:  1966-04       Impact factor: 11.205

Review 4.  Separation of subcellular particles.

Authors:  A P Mathias
Journal:  Br Med Bull       Date:  1966-05       Impact factor: 4.291

5.  Induction in vitro of antibodies to phage T2: antigens in the RNA extract employed.

Authors:  H P Friedman; A B Stavitsky; J M Solomon
Journal:  Science       Date:  1965-09-03       Impact factor: 47.728

6.  Antibody formation initiated in vitro. 3. Antibody formation and allotypic specificity directed by ribonucleic acid from peritoneal exudate cells.

Authors:  F L Adler; M Fishman; S Dray
Journal:  J Immunol       Date:  1966-10       Impact factor: 5.422

7.  Immunogenicity of a series of alpha,N-DNP-L-lysines.

Authors:  S F Schlossman; A Yaron; S Ben-Efraim; H A Sober
Journal:  Biochemistry       Date:  1965-08       Impact factor: 3.162

8.  Helix-coil transition of polyl-glutamic acid and polyl-lysine in D2O.

Authors:  P Appel; J T Yang
Journal:  Biochemistry       Date:  1965-07       Impact factor: 3.162

9.  Genetic control of the antibody response. I. Demonstration of determinant-specific differences in response to synthetic polypeptide antigens in two strains of inbred mice.

Authors:  H O McDevitt; M Sela
Journal:  J Exp Med       Date:  1965-09-01       Impact factor: 14.307

10.  The behavior of hapten-poly-L-lysine conjugates as complete antigens in genetic responder and as haptens in nonresponder guinea pigs.

Authors:  I Green; W E Paul; B Benacerraf
Journal:  J Exp Med       Date:  1966-05-01       Impact factor: 14.307

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  8 in total

Review 1.  Gene activation during immune reaction.

Authors:  D Jachertz
Journal:  Mol Cell Biochem       Date:  1979-03-19       Impact factor: 3.396

Review 2.  Studies of antigen-RNA and immunity.

Authors:  J S Garvey; E B Reilly
Journal:  Mol Cell Biochem       Date:  1979-03-05       Impact factor: 3.396

3.  Distribution of antigen fragments of IgG among the nucleotides of RNA.

Authors:  D Nachkov; L Wassilewa; K Tsankova; L Christophorov
Journal:  Experientia       Date:  1973-02-15

4.  Uptake of radioiodinated antigens by human monocytes.

Authors:  S E Salmon; V B Morhenn; M J Cline
Journal:  Clin Exp Immunol       Date:  1971-03       Impact factor: 4.330

5.  Preliminary characterization of "immunogenic" ribonucleic acid derived from rat peritoneal exudate cells.

Authors:  S J Archer; C J Wust
Journal:  Infect Immun       Date:  1973-08       Impact factor: 3.441

6.  The immunogenicity of antigen bound to the plasma membrane of macrophages.

Authors:  E R Unanue; J C Cerottini
Journal:  J Exp Med       Date:  1970-04-01       Impact factor: 14.307

7.  Potentiation of the T-lymphocyte response to mitogens. II. The cellular source of potentiating mediator(s).

Authors:  I Gery; B H Waksman
Journal:  J Exp Med       Date:  1972-07-01       Impact factor: 14.307

8.  The interaction of soluble horseradish peroxidase with mouse peritoneal macrophages in vitro.

Authors:  R M Steinman; Z A Cohn
Journal:  J Cell Biol       Date:  1972-10       Impact factor: 10.539

  8 in total

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