Literature DB >> 131176

Antigen-initiated B-lymphocyte differentiation. VIII. Sedimentation velocity and buoyant density characterization of virgin antibody-forming cell progenitors in the adoptive immune response of unprimed CBA mice to 4-hydroxy-3-iodo-5-nitrophenylacetic acid-polymerized bacterial flagellin antigen.

J M Fidler, M C Howard, K Shortman.   

Abstract

The characteristics of antibody-forming cell (AFC) progenitors lacking previous contact with specific antigen (virgin AFC progenitors) has been studied using sedimentation velocity and buoyant density separation for the investigation of physically distinct B-cell subpopulations. Functional characterization of isolated subsets was made using a quantitative adoptive immune assay for the IgM AFC progenitors responding to the antigen 4-hydroxy-3-iodo-5-nitrophenylacetic acid conjugated polymerized bacterial flagellin. Extensive heterogeneity is present among B lymphocytes, only some subpopulations of which exhibit AFC progenitor function. In the spleen of adult conventional CBA mice, atypically fast sedimenting cells of low buoyant density are active, while typical small B lymphocytes do not appear to be progenitors of IgM AFC. Spleen of adult specific pathogen-free (SPF), germfree, and athymic nude mice give similar results, although a minor population of typical slowly sedimenting dense cells are active in the latter two sources. Adult conventional bone marrow cells are as physically and functionally heterogeneous as splenic B cells, and although a significant proportion of AFC progenitor activity is found among dense, slowly sedimenting cells, most of the activity is among low density, faster sedimenting cells. In contrast to this situation in adult animals, where most of the unprimed AFC progenitors are large, atypical B cells, the spleens of neonatal mice provide a site where virgin AFC progenitors with the physical properties of typical small B lymphocytes are found. While being present in conventional and SPF neonatal spleens, these virgin cells are predominant in 7-day-old germfree mouse spleen. These findings suggest that the newborn virgin B cell is a typical small lymphocyte. However, few cells of this type are found in the adult animal. The unprimed AFC-progenitor population in the adult consists of large, fast sedimenting, low buoyant density, adherent cells, the physical properties of which are characteristic of activated B lymphocytes. It is suggested that these atypical cells are derived from the small newborn virgin B cell by the nonspecific effects of environmental antigenic stimuli.

Entities:  

Mesh:

Substances:

Year:  1976        PMID: 131176      PMCID: PMC2190190          DOI: 10.1084/jem.143.5.1220

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


  37 in total

Review 1.  T cell control of antibody production.

Authors:  R K Gershon
Journal:  Contemp Top Immunobiol       Date:  1974

Review 2.  Physical procedures for the separation of animal cells.

Authors:  K Shortman
Journal:  Annu Rev Biophys Bioeng       Date:  1972

3.  Evidence for the existence of multipotential lympho-hematopoietic stem cells in adult rat.

Authors:  P C Nowell; B E Hirsch; D H Fox; D B Wilson
Journal:  J Cell Physiol       Date:  1970-04       Impact factor: 6.384

4.  The migration of lymphocytes from bone marrow to popliteal lymph nodes demonstrated by selective bone marrow labeling with 3 H-thymidine in vivo.

Authors:  F Brahim; D G Osmond
Journal:  Anat Rec       Date:  1973-04

5.  The separation of different cell classes from lymphoid organs. II. The purification and analysis of lymphocyte populations by equilibrium density gradient centrifugation.

Authors:  K Shortman
Journal:  Aust J Exp Biol Med Sci       Date:  1968-08

6.  Antibody production by mice repopulated with limited numbers of clones of lymphoid cell precursors.

Authors:  J Trentin; N Wolf; V Cheng; W Fahlberg; D Weiss; R Bonhag
Journal:  J Immunol       Date:  1967-06       Impact factor: 5.422

7.  Antigen-initiated B lymphocyte differentiation. V. Electrophoretic separation of different subpopulations of AFC progenitors for unprimed IgM and memory IgG responses to the NIP determinant.

Authors:  R A Schlegel; H von Boehmer; K Shortman
Journal:  Cell Immunol       Date:  1975-03       Impact factor: 4.868

8.  Differentiation of lymphocytes in mouse bone marrow. II. Kinetics of maturation and renewal of antiglobulin-binding cells studied by double labeling.

Authors:  D G Osmond; G J Nossal
Journal:  Cell Immunol       Date:  1974-07       Impact factor: 4.868

9.  The in vitro immune response to sheep erythrocytes by fractionated spleen cells: biological and immunological differences.

Authors:  J S Haskill; J Marbrook
Journal:  J Immunol Methods       Date:  1971-09       Impact factor: 2.303

10.  A quantitative assay for the progenitors of bone marrow-associated lymphocytes.

Authors:  L Lafleur; R G Miller; R A Phillips
Journal:  J Exp Med       Date:  1972-06-01       Impact factor: 14.307

View more
  5 in total

1.  Heteroantisera prepared against B lymphocytes at different stages of differentiation. II. Functional analysis of cytotoxicity to different B-cell populations.

Authors:  R M Gorczynski
Journal:  Immunology       Date:  1977-05       Impact factor: 7.397

Review 2.  A revisionist history of adult marrow stem cell biology or 'they forgot about the discard'.

Authors:  P Quesenberry; L Goldberg
Journal:  Leukemia       Date:  2017-05-22       Impact factor: 11.528

3.  Activation of B chronic lymphocytic leukaemia cells by Branhamella catarrhalis.

Authors:  J E Calvert; S J Proctor; R Jefferis
Journal:  Immunology       Date:  1987-01       Impact factor: 7.397

4.  Characteristics of human B cells responsive to the T-independent mitogen Branhamella catarrhalis.

Authors:  J E Calvert; A Calogeras
Journal:  Immunology       Date:  1986-05       Impact factor: 7.397

5.  Defective colony formation by B lymphocytes from CBA/N and C3H/HeJ mice.

Authors:  P W Kincade
Journal:  J Exp Med       Date:  1977-02-01       Impact factor: 14.307

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.