Literature DB >> 521634

Use and functional properties of peripheral blood lymphocytes in mice.

P Chandler, T Matsunaga, D Benjamin, E Simpson.   

Abstract

Peripheral blood lymphocytes (PBL) were isolated and examined for their ability to respond in vitro to H-2 and H-Y antigens and also to hapten conjugated syngeneic cells. In addition, these lymphocytes were tested as antigen and target cells in in vitro mixed lymphocyte reaction and in chromium release cell mediated lympholysis respectively, as well as serving as targets for the H-2 typing of chimeric mice. Two methods were used to isolate the lymphocytes: a density gradient separation and a double water lysis technique. PBL, prepared by either method compared favourably with splenic lymphocytes in all aspects of anti-H-2 cytotoxicity but could not be used as responder for anti-H-Y cytotoxicity. In addition a method has been developed using PBL as targets for H-2 typing of both allophenic and irradiation chimeric mice. The small numbers of cells required for each of these procedures allows for the preselection of suitable mice and/or multiple experimental determinations on individual mice.

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Year:  1979        PMID: 521634     DOI: 10.1016/0022-1759(79)90147-9

Source DB:  PubMed          Journal:  J Immunol Methods        ISSN: 0022-1759            Impact factor:   2.303


  3 in total

1.  H-Y antigen in Sxr mice detected by H-2-restricted cytotoxic T cells.

Authors:  E Simpson; P Edwards; S Wachtel; A McLaren; P Chandler
Journal:  Immunogenetics       Date:  1981       Impact factor: 2.846

2.  Special proliferative sites are not needed for seeding and proliferation of transfused bone marrow cells in normal syngeneic mice.

Authors:  G Brecher; J D Ansell; H S Micklem; J H Tjio; E P Cronkite
Journal:  Proc Natl Acad Sci U S A       Date:  1982-08       Impact factor: 11.205

3.  Development of B lymphocytes in mice heterozygous for the X-linked immunodeficiency (xid) mutation. xid inhibits development of all splenic and lymph node B cells at a stage subsequent to their initial formation in bone marrow.

Authors:  L M Forrester; J D Ansell; H S Micklem
Journal:  J Exp Med       Date:  1987-04-01       Impact factor: 14.307

  3 in total

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