Literature DB >> 1569396

The extent of clonal structure in different lymphoid organs.

M H Hermans1, A Wubbena, F G Kroese, S V Hunt, R Cowan, D Opstelten.   

Abstract

To gain insight into the clonal organization of lymphoid organs, we studied the distribution in situ of donor-derived cells in near-physiological chimeras. We introduced RT7b fetal liver cells into nonirradiated congenic RT7a neonatal rats. The chimerism 6-20 wk after injection ranged from 0.3 to 20%. The numbers of cell clones simultaneously contributing to cell generation in a particular histological feature were deduced from the variance in donor cell distribution. In bone marrow and thymus, donor-derived lymphoid cells were found scattered among host cells, indicating a high mobility of cells. In bone marrow, donor cells were evenly distributed over the entire marrow, even at low chimerism. This indicates that leukopoiesis is maintained by the proliferation of many clones. In the thymus, the various lobules showed different quantities of donor-derived lymphoid cells. Mathematical analysis of these differences indicated that 17-18 cell division cycles occur in the cortex. In spleen, the distribution of donor-derived cells over the germinal centers indicated that 5 d after antigenic stimulation, germinal centers develop oligoclonally. The main conclusions of this work are that (a) bone marrow and thymus are highly polyclonal; (b) 17-18 divisions occur between prothymocyte and mature T cell; and (c) lymphoid cells disperse rapidly while proliferating and differentiating.

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Year:  1992        PMID: 1569396      PMCID: PMC2119216          DOI: 10.1084/jem.175.5.1255

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


  63 in total

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Authors:  D B Thomas; C M Smith; J M Sumpster
Journal:  J Anat       Date:  1976-09       Impact factor: 2.610

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3.  B lymphocyte-associated antigens on terminal deoxynucleotidyl transferase-positive cells and pre-B cells in bone marrow of the rat.

Authors:  D Opstelten; G J Deenen; J Rozing; S V Hunt
Journal:  J Immunol       Date:  1986-07-01       Impact factor: 5.422

4.  Numbers and dispersion of repopulating hematopoietic cell clones in radiation chimeras as functions of injected cell dose.

Authors:  H S Micklem; J E Lennon; J D Ansell; R A Gray
Journal:  Exp Hematol       Date:  1987-03       Impact factor: 3.084

5.  Deletion of self-reactive T cells before entry into the thymus medulla.

Authors:  H Hengartner; B Odermatt; R Schneider; M Schreyer; G Wälle; H R MacDonald; R M Zinkernagel
Journal:  Nature       Date:  1988-11-24       Impact factor: 49.962

6.  T-lymphocytes in rat lymphoid follicles are a subset of T helper cells.

Authors:  F G Kroese; A S Wubbena; P Joling; P Nieuwenhuis
Journal:  Adv Exp Med Biol       Date:  1985       Impact factor: 2.622

7.  Germinal centers develop oligoclonally.

Authors:  F G Kroese; A S Wubbena; H G Seijen; P Nieuwenhuis
Journal:  Eur J Immunol       Date:  1987-07       Impact factor: 5.532

8.  Fluorescence analysis and anatomic distribution of mouse T lymphocyte subsets defined by monoclonal antibodies to the antigens Thy-1, Lyt-1, Lyt-2, and T-200.

Authors:  W van Ewijk; P L van Soest; G J van den Engh
Journal:  J Immunol       Date:  1981-12       Impact factor: 5.422

9.  Large numbers of primitive stem cells are active simultaneously in aggregated embryo chimeric mice.

Authors:  D E Harrison; C Lerner; P C Hoppe; G A Carlson; D Alling
Journal:  Blood       Date:  1987-03       Impact factor: 22.113

10.  The MRC OX-44 antigen marks a functionally relevant subset among rat thymocytes.

Authors:  D J Paterson; J R Green; W A Jefferies; M Puklavec; A F Williams
Journal:  J Exp Med       Date:  1987-01-01       Impact factor: 14.307

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3.  How oligoclonal are germinal centers? A new method for estimating clonal diversity from immunohistological sections.

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  3 in total

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