Literature DB >> 7451964

Analysis of NZB hyperdiploid spleen cells.

E S Raveche, O Alabaster, J H Tjio, J Taurog, A D Steinberg.   

Abstract

In order to study the cell types involved in the hyperdiploidy characteristic of NZB mice, flow cytometric techniques, which measure te DNA content of individual cells, have been used together with standard cytogenetic analysis. The aneuploid cells present in NZB mice were found to be clonally derived. These cells were of large size relative to nonaneuploid cells. They could not be removed by lysis with anti-Thy 1 plus complement nor were they present in the nylon-wool column nonadherent fraction, both of which are characteristic of T cells. By further cytotoxic analysis, the aneuploid cells were found not to express Ly-5 nor NK surface antigens, found on natural killer cells. The aneuploid cells had increased quantities of cell surface H-2 antigen. This marked susceptibility to lysis with anti-H-2 serum was associated with one or more extra copies of chromosome 17, which carries the H-2 complex. A large proportion of these cells also expressed surface Ia and Ig. The aneuploid cells found in the spleens of older NZB mice derive from bone marrow stem cells. Neonatally thymectomized and lethally irradiated NZB X DBA/2 recipients of anti-Thy-1 treated young NZB bone marrow cells ultimately developed aneuploid spleen cells. Such cells are not found in intact or thymectomized NZB Z DBA/2 mice nor in recipients of DBA/2 marrow. Finally, congenic NZB mice carrying the CBZ/N xid failed to develop aneuploidy. Taken together, these studies suggest that the aneuploid cell is a bone marrow-derived stem cell destined to differentiate into the B cell subset lacking in CBA/N mice.

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Year:  1981        PMID: 7451964

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  5 in total

1.  Polyclonal B cell activation in lupus-prone mice precedes and predicts the development of autoimmune disease.

Authors:  D M Klinman
Journal:  J Clin Invest       Date:  1990-10       Impact factor: 14.808

Review 2.  Murine models of chronic lymphocytic leukaemia: role of microRNA-16 in the New Zealand Black mouse model.

Authors:  Brian J Scaglione; Erica Salerno; Murugabaskar Balan; Frederick Coffman; Pablo Landgraf; Fatima Abbasi; Sergei Kotenko; Gerald E Marti; Elizabeth S Raveche
Journal:  Br J Haematol       Date:  2007-10-17       Impact factor: 6.998

3.  Clonal expansion of abnormal B cells in old NZB mice.

Authors:  M F Seldin; J Conroy; A D Steinberg; L A D'Hoosteleare; E S Raveche
Journal:  J Exp Med       Date:  1987-11-01       Impact factor: 14.307

4.  Genetic studies in NZB mice. V. Recombinant inbred lines demonstrate that separate genes control autoimmune phenotype.

Authors:  E S Raveche; E A Novotny; C T Hansen; J H Tjio; A D Steinberg
Journal:  J Exp Med       Date:  1981-05-01       Impact factor: 14.307

5.  Oncogene expression in autoimmune and normal peripheral blood mononuclear cells.

Authors:  D M Klinman; J F Mushinski; M Honda; Y Ishigatsubo; J D Mountz; E S Raveche; A D Steinberg
Journal:  J Exp Med       Date:  1986-05-01       Impact factor: 14.307

  5 in total

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