Literature DB >> 1937566

Reciprocal haematopoietic cell transfers between C57BL/6 mice differing at the lpr locus.

E M Montecino-Rodriguez1, F Loor.   

Abstract

Reciprocal transfers of spleen and bone marrow cell suspensions have been performed between mice of the C57BL/6 (B6) genetic background, differing at the lymphoproliferation (lpr) locus. These immune system chimaeras were followed for almost one year after sublethal irradiation and cell reconstitution. In addition to the survival of the chimaeras, the major lymphoid organs (bone marrow, spleen, thymus and lymph nodes) were examined for cell numbers, percentages of membrane immunoglobulin-positive cells and responses to mitogenic stimulations with concanavalin and lipopolysaccharide. The [lpr----lpr] chimaeras were similar to untreated lpr mice. The [wild----lpr] did not develop the lpr-induced syndrome and remained similar to [wild----wild] chimaeras. Therefore, B6 wild haematopoietic stem cells could rescue sublethally irradiated B6 lpr mice from the lpr-induced autoimmune pathology. The radioresistant lpr environment alone was not sufficient to induce the lpr syndrome. It may however be required for its development since [lpr----wild] chimaeras displayed a profound aplasia of their lymphoid organs, together with a normal cellularity of their bone marrow. In contrast to chimaeras constructed with MRL mice, the [lpr----wild] B6 chimaeras did not die following the lpr haematopoietic stem cell transfer. Therefore, the lymphoid aplasia of [lpr----wild] radiation chimaeras does not result from an lpr graft-versus-host-like syndrome. More likely is that a normal, non-lpr, haematopoietic environment may not allow the differentiation of the lpr haematopoietic stem cells into the lymphoid lineages.

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Year:  1991        PMID: 1937566      PMCID: PMC1384681     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  17 in total

1.  Treatment of donor cells with L-leucyl-L-leucine methyl ester prevents induction of graft-vs-host-like reaction in [lpr/lpr----+/+] chimera.

Authors:  H Okuyama; S Kobayashi; H Harada; Y Kawaguchi; I Sekikawa
Journal:  Clin Immunol Immunopathol       Date:  1990-01

2.  Mechanism of L-leucyl-L-leucine methyl ester-mediated killing of cytotoxic lymphocytes: dependence on a lysosomal thiol protease, dipeptidyl peptidase I, that is enriched in these cells.

Authors:  D L Thiele; P E Lipsky
Journal:  Proc Natl Acad Sci U S A       Date:  1990-01       Impact factor: 11.205

3.  Histopathologic sequence of events in adult mice undergoing lethal graft-versus-host reaction developed across H-2 and/or non-H-2 histocompatibility barriers.

Authors:  H Rappaport; A Khalil; O Halle-Pannenko; L Pritchard; D Dantchev; G Mathé
Journal:  Am J Pathol       Date:  1979-07       Impact factor: 4.307

4.  Selective elimination of non-lpr lymphoid cells in mice undergoing lpr-mediated graft-vs-host disease.

Authors:  D L Perkins; J Michaelson; R M Glaser; A Marshak-Rothstein
Journal:  J Immunol       Date:  1987-09-01       Impact factor: 5.422

5.  Evidence for an intrinsic B cell defect in lpr/lpr mice apparent in neonatal chimeras.

Authors:  D L Perkins; R M Glaser; C A Mahon; J Michaelson; A Marshak-Rothstein
Journal:  J Immunol       Date:  1990-07-15       Impact factor: 5.422

6.  Generalized toxicity of L-leucyl-leucine-methyl ester for lymphocyte functions.

Authors:  A M Mowat; P A Leck
Journal:  Immunology       Date:  1990-04       Impact factor: 7.397

7.  The influence of IL-1 treatment on the reconstitution of the hemopoietic and immune systems after sublethal radiation.

Authors:  P Morrissey; K Charrier; L Bressler; A Alpert
Journal:  J Immunol       Date:  1988-06-15       Impact factor: 5.422

8.  The lpr gene is associated with resistance to engraftment by lymphoid but not erythroid stem cells from normal mice.

Authors:  D L Perkins; J Michaelson; A Marshak-Rothstein
Journal:  J Immunol       Date:  1987-01-15       Impact factor: 5.422

9.  Long-term observations of autoimmune-prone mice treated for autoimmune disease by allogeneic bone marrow transplantation.

Authors:  S Ikehara; R Yasumizu; M Inaba; S Izui; K Hayakawa; K Sekita; J Toki; K Sugiura; H Iwai; T Nakamura
Journal:  Proc Natl Acad Sci U S A       Date:  1989-05       Impact factor: 11.205

10.  Lethal graft-versus-host disease after bone marrow transplantation across minor histocompatibility barriers in mice. Prevention by removing mature T cells from marrow.

Authors:  R Korngold; J Sprent
Journal:  J Exp Med       Date:  1978-12-01       Impact factor: 14.307

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  4 in total

1.  Haematopoietic cell transfers between C57BL/6 mice differing at the lpr or gld locus.

Authors:  E M Montecino-Rodriguez; F Loor
Journal:  Immunology       Date:  1991-09       Impact factor: 7.397

2.  Influence of the lpr environment on the lymph node cell phenotypes in C57BL/6 nubg and nulpr chimeras.

Authors:  F Tiberghien; R Ceredig; F Loor
Journal:  Immunology       Date:  1994-12       Impact factor: 7.397

3.  Lack of transfer of lpr-type abnormalities (lymphoproliferation or lymphoid aplasia) in double congenic nude beige mice engrafted with lpr haematopoietic cells.

Authors:  F Tiberghien; F Pflumio; L Kuntz; F Loor
Journal:  Immunology       Date:  1993-05       Impact factor: 7.397

4.  Significant role of Fas ligand-binding but defective Fas receptor (CD95) in lymph node hyperplasia composed of abnormal double-negative T cells.

Authors:  Akio Matsuzawa; Motomu Shimizu; Yasutaka Takeda; Hisashi Nagase; Kazutoshi Sayama; Mikio Kimura
Journal:  Immunology       Date:  2002-08       Impact factor: 7.397

  4 in total

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