Literature DB >> 5334544

The ultrastructure and function of the cells in lymph following antigenic stimulation.

J G Hall, B Morris, G D Moreno, M C Bessis.   

Abstract

When a lymph node receives an antigenic stimulus the cell population in the efferent lymph changes and large basophilic cells appear. During a secondary immune response cells of this type may account for over 50% of the cells present in lymph. When examined by electron microscopy, many of these cells were found to be primitive undifferentiated blast cells with many free ribosomes in their cytoplasm and only an occasional piece of endoplasmic reticulum. Their nuclear chromatin was sparse and the nuclei contained several nucleoli. Many other cells which were judged to be more differentiated had large numbers of ribosomes arranged in clusters which took the form of rosettes or spirals. These cells also had more ergastoplasm but this occurred usually in the form of short pieces of disorganized endoplasmic reticulum. No cells with the ultrastructure of classical plasma cells were found in efferent lymph although these cells were abundant in the stimulated lymph nodes. It was shown that when the lymph which contained these cells was collected quantitatively no systemic immunity developed even though a vigorous immune response took place in the lymph node with the formation of many plasma cells. Failure of the systemic immune response to develop could not be explained merely in terms of the loss of antibody. It was concluded that these basophilic cells rather than antigen are responsible for propagating the immune response throughout the body and that they depend on an intact lymphatic pathway for their immediate transport. This view was supported by experiments which showed that these cells are capable of initiating immune responses in other lymph nodes of the same animal and of transferring active immunity between chimeric twins. The most likely explanation of these results is that the basophilic lymphoid cells carry out their messenger function by developing into plasma cells at sites remote from the site at which antigen is localized. However this has yet to be proven and the possibility remains that these mobile, highly motile, RNA-rich cells may express their messenger function by transferring information to other effector cells.

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Year:  1967        PMID: 5334544      PMCID: PMC2138347          DOI: 10.1084/jem.125.1.91

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


  24 in total

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Authors:  J G HALL; B MORRIS
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Authors:  J G HALL; B MORRIS
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4.  Surgical techniques for the collection of lymph from unanaesthetized sheep.

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6.  Studies on the rôle of lymphocytes in antibody production.

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Journal:  Acta Derm Venereol       Date:  1952       Impact factor: 4.437

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

Authors:  A J Cunningham; J B Smith; E H Mercer
Journal:  J Exp Med       Date:  1966-10-01       Impact factor: 14.307

8.  THE ORIGIN OF THE CELLS IN THE EFFERENT LYMPH FROM A SINGLE LYMPH NODE.

Authors:  J G HALL; B MORRIS
Journal:  J Exp Med       Date:  1965-06-01       Impact factor: 14.307

9.  Cytochemistry and electron microscopy. The preservation of cellular ultrastructure and enzymatic activity by aldehyde fixation.

Authors:  D D SABATINI; K BENSCH; R J BARRNETT
Journal:  J Cell Biol       Date:  1963-04       Impact factor: 10.539

10.  STUDIES ON ANTIBODY PRODUCTION. IX. THE CELLULAR LOCALIZATION OF ANTIGEN MOLECULES (FERRITIN) IN THE SECONDARY RESPONSE.

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Journal:  J Exp Med       Date:  1964-04-01       Impact factor: 14.307

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  47 in total

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2.  Intracellular distribution of antibody in immunocytes responding to primary challenge with horseradish peroxidase.

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

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4.  Blood microcirculation in the lymph node in xanthomatosis.

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5.  Ontogenetic development of antibody formation in response to different doses of gram-negative microorganisms in young rabbits. II. The relationship between the secondary reaction and primary antigen dose and an attempt to induce tolerance.

Authors:  J Medlín; H Tlaskalová; J Sterzl
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6.  The in vivo functions and properties of persisting cell-stimulating factor.

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Journal:  Immunology       Date:  1984-09       Impact factor: 7.397

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8.  Lymphocyte emigration from lymph nodes by blood in the pig and efferent lymph in the sheep.

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9.  Distribution of plaque-forming cells in the mouse for a protein antigen. Evidence for highly active parathymic lymph nodes following intraperitoneal injection of hen lysozyme.

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Journal:  Immunology       Date:  1976-06       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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