Literature DB >> 3155688

Capacity of small B cell-enriched populations to stimulate mixed lymphocyte reactions: marked differences between irradiated vs. mitomycin C-treated stimulators.

S R Webb, J H Li, D B Wilson, J Sprent.   

Abstract

To investigate whether small B cells can stimulate mixed lymphocyte reactions (MLR), highly purified populations of large vs. small B cell fractions were tested for their capacity to evoke MLR across Mls vs. H-2 barriers. Large B cell fractions stimulated high MLR to Mls and H-2 determinants, irrespective of whether the stimulators were exposed to irradiation or pretreated with mitomycin C. In accord with the findings of others, irradiated small B cell fractions proved to be very poor stimulators of MLR. Significantly, however, mitomycin C-treated small B cell fractions elicited high MLR, particularly to Mls determinants. The finding that small B cell fractions treated with irradiation are poor stimulators of T cells correlates with the known radiosensitivity of B cells. In this respect, the widely held view that small B cells do not have antigen-presenting cell (APC) function rests largely on studies with irradiated B cells. The present finding that T cells respond well to small B cells treated with mitomycin C, however, indicates that small B cell fractions do have APC function. Whether the APC function of small B cells reflects a response to resting B cells per se rather than to cells undergoing activation in vitro, however, remains to be ascertained.

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Year:  1985        PMID: 3155688     DOI: 10.1002/eji.1830150118

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  15 in total

1.  DBA/2J (Mls-1a) B-cell differentiation in BALB.xid recipients.

Authors:  K Tocce; K Suppiah; C Rago; R Liberchuk; K Duffy; J Riggs
Journal:  Immunology       Date:  2000-01       Impact factor: 7.397

Review 2.  Antigen presenting cells.

Authors:  D L Hamilos
Journal:  Immunol Res       Date:  1989       Impact factor: 2.829

3.  Multi-gene/allele control of Mlsb of CBA/H.

Authors:  R E Click; A Adelmann
Journal:  Immunogenetics       Date:  1989       Impact factor: 2.846

4.  Allostimulatory analysis of a newly-defined and widely-distributed Mls superantigen.

Authors:  J J Ryan; H B LeJeune; J J Mond; F D Finkelman
Journal:  Immunogenetics       Date:  1991       Impact factor: 2.846

5.  Functional and epigenetic studies reveal multistep differentiation and plasticity of in vitro-generated and in vivo-derived follicular T helper cells.

Authors:  Kristina T Lu; Yuka Kanno; Jennifer L Cannons; Robin Handon; Paul Bible; Abdel G Elkahloun; Stacie M Anderson; Lai Wei; Hongwei Sun; John J O'Shea; Pamela L Schwartzberg
Journal:  Immunity       Date:  2011-10-20       Impact factor: 31.745

6.  The expression of Mlsc determinants on Mlsa, Mlsb, and Mlsx prototypic strains.

Authors:  R Abe; R J Hodes
Journal:  Immunogenetics       Date:  1988       Impact factor: 2.846

7.  Multigene control of Mlsc.

Authors:  R E Click; A Adelmann
Journal:  Immunogenetics       Date:  1988       Impact factor: 2.846

8.  H-2-linked genes determine the level of the primary in vitro anti-Mls response.

Authors:  S Macphail; O Stutman
Journal:  Immunogenetics       Date:  1986       Impact factor: 2.846

9.  Clonal analysis of the Mls system. A reappraisal of polymorphism and allelism among Mlsa, Mlsc, and Mlsd.

Authors:  R Abe; J J Ryan; R J Hodes
Journal:  J Exp Med       Date:  1987-04-01       Impact factor: 14.307

10.  Restricted tissue distribution of Mlsa determinants. Stimulation of Mlsa-reactive T cells by B cells but not by dendritic cells or macrophages.

Authors:  S R Webb; A Okamoto; Y Ron; J Sprent
Journal:  J Exp Med       Date:  1989-01-01       Impact factor: 14.307

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