Literature DB >> 5950889

Antibody formation by single cells from lymph nodes and efferent lymph of sheep.

A J Cunningham, J B Smith, E H Mercer.   

Abstract

The antibody-forming cells which appear in the popliteal lymph node and efferent lymph of the sheep following immunization with boiled Salmonella have been studied by light and electron microscopy. Cells were incubated in monolayers with target erythrocytes sensitized with bacterial lipopolysaccharide. Three types of interaction between a proportion of the lymph cells and the erythrocytes surrounding them have been shown to indicate antibody formation: plaque-formation, immuno-cyto-adherence, and localized agglutination. At the peak of the response, 4 days after antigenic stimulation approximately 1 cell in every 200 from lymph node suspensions produces detectable specific antibody, while up to 1 cell in 20 in the lymph is active. For light microscope examination, individual antibody-forming cells were smeared in serum and stained with Leishman's stain. For electron microscopy, a number of active cells were clumped with antiserum to form a specimen of convenient size, then sectioned. Most of the active cells from efferent lymph are large and basophilic, while a small proportion are blastlike. These cells contain abundant free ribosomes and very little endoplasmic reticulum. In the node only, an additional class of antibody-forming plasma cells is found which have considerable amounts of endoplasmic reticulum in their cytoplasm.

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Year:  1966        PMID: 5950889      PMCID: PMC2138246          DOI: 10.1084/jem.124.4.701

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


  24 in total

1.  A SIMPLE METHOD FOR DETECTING SINGLE ANTIBODY-FORMING CELLS.

Authors:  O B ZAALBERG
Journal:  Nature       Date:  1964-06-20       Impact factor: 49.962

2.  MORPHOLOGICAL AND KINETIC STUDIES ON ANTIBODY-PRODUCING CELLS IN RAT LYMPH NODES.

Authors:  B M BALFOUR; E H COOPER; E L ALPEN
Journal:  Immunology       Date:  1965-03       Impact factor: 7.397

3.  The lymph-borne cells of the immune response.

Authors:  J G HALL; B MORRIS
Journal:  Q J Exp Physiol Cogn Med Sci       Date:  1963-07

4.  Helical arrangement of ribosomes in differentiating muscle cells.

Authors:  C H WADDINGTON; M M PERRY
Journal:  Exp Cell Res       Date:  1963-05       Impact factor: 3.905

5.  The formation of macroglobulin antibodies. I. Studies on adult humans.

Authors:  J LOSPALLUTO; W MILLER; B DORWARD; C W FINK
Journal:  J Clin Invest       Date:  1962-07       Impact factor: 14.808

6.  A method for electron microscopic examination of antibody-producing cells.

Authors:  A J Cunningham; J B Smith; E H Mercer
Journal:  Immunology       Date:  1966-11       Impact factor: 7.397

7.  A method of increased sensitivity for detecting single antibody-forming cells.

Authors:  A J Cunningham
Journal:  Nature       Date:  1965-09-04       Impact factor: 49.962

8.  Plaque Formation in Agar by Single Antibody-Producing Cells.

Authors:  N K Jerne; A A Nordin
Journal:  Science       Date:  1963-04-26       Impact factor: 47.728

9.  Electron microscopic observations on antibody-producing lymph node cells.

Authors:  T N Harris; K Hummeler; S Harris
Journal:  J Exp Med       Date:  1966-01-01       Impact factor: 14.307

10.  THE CELLULAR ORIGIN OF HUMAN IMMUNOGLOBULINS (GAMMA-2, GAMMA-1M, GAMMA-1A).

Authors:  R C MELLORS; L KORNGOLD
Journal:  J Exp Med       Date:  1963-09-01       Impact factor: 14.307

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  38 in total

1.  Differing effects of dietary protein deprivation on the production of rosette-forming cells in the lymph nodes and the spleen and on the levels of serum haemagglutinins in rats immunized to sheep red cells.

Authors:  A Aschkenasy
Journal:  Immunology       Date:  1973-04       Impact factor: 7.397

2.  Quantitative studies on the proliferation and differentiation of antibody-forming cells in lymph.

Authors:  J B Hay; M J Murphy; B Morris; M C Bessis
Journal:  Am J Pathol       Date:  1972-01       Impact factor: 4.307

3.  Antigenic characterization of murine rosette and plaque-forming cells.

Authors:  R Laskov; R Rabinowitz; M Schlesinger
Journal:  Immunology       Date:  1973-06       Impact factor: 7.397

4.  Electrophoretic analysis of antibody produced by single cells.

Authors:  J J Marchalonis; G J Nossal
Journal:  Proc Natl Acad Sci U S A       Date:  1968-11       Impact factor: 11.205

5.  In vitro stimulation of antibody formation by peritoneal cells. 3. Effect of active immunization on the subsequent in vitro performance of peritoneal and spleen cells.

Authors:  S Boris; A E Bussard; S Deutsch; G J Nossal
Journal:  Immunology       Date:  1970-11       Impact factor: 7.397

6.  An improved assay for haemolytic plaque-forming cells.

Authors:  J C Kennedy; M A Axelrad
Journal:  Immunology       Date:  1971-02       Impact factor: 7.397

7.  Functional symmetry amongst daughter cells arising in vitro from single antibody-forming cells.

Authors:  G J Nossal; H Lewis
Journal:  Immunology       Date:  1971-05       Impact factor: 7.397

8.  Cytodynamics of the immune response in two lines of mice genetically selected for "high" and "low" antibody synthesis.

Authors:  G Biozzi; C Stiffel; D Mouton; Y Bouthillier; C Decreusefond
Journal:  J Exp Med       Date:  1972-05-01       Impact factor: 14.307

9.  Inhibition of lymphocyte growth by Ulex seed extracts (USE).

Authors:  B Pirofsky; R Beaulieu; G H Davies
Journal:  Immunology       Date:  1981-08       Impact factor: 7.397

10.  Hyperbasophilic immunoblasts in circulating blood in chronic inflammatory rheumatic and collagen diseases.

Authors:  F Delbarre; A Le Gô; A Kahan
Journal:  Ann Rheum Dis       Date:  1975-10       Impact factor: 19.103

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