Abstract
Ig+ spleen cells were analysed by light scatter analysis on a flow cytometer and two distinct subpopulations were identified. The large Ig+ cells (10-11 micron in diameter) were found in spleen and bone marrow, whereas the small Ig+ cells (7-8 micron in diameter) were found in all lymphoid tissues. Of the total Ig+ splenic lymphocytes, 40-60% were large Ig+ cells and had surface IgM, Ia and Fc gamma receptors. The large Ig+ cells were highly enriched for responsiveness to the B-cell mitogens, anti-Ig, Nocardia water-soluble mitogen and LPS, whereas the small Ig+ splenic cells had little or no responsiveness to these mitogens.
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- Ahmed A., Scher I., Sharrow S. O., Smith A. H., Paul W. E., Sachs D. H., Sell K. W. B-lymphocyte heterogeneity: development and characterization of an alloantiserum which distinguishes B-lymphocyte differentiation alloantigens. J Exp Med. 1977 Jan 1;145(1):101–110. doi: 10.1084/jem.145.1.101. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Anderson J., Melchers F. T cell-dependent activation of resting B cells: requirement for both nonspecific unrestricted and antigen-specific Ia-restricted soluble factors. Proc Natl Acad Sci U S A. 1981 Apr;78(4):2497–2501. doi: 10.1073/pnas.78.4.2497. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Birch R. E., Bernier G. M., Fanger M. W. Lymphocytes in the rabbit expressing receptors for the Fc portion of rabbit immunoglobulin. J Immunol. 1978 Jun;120(6):1869–1875. [PubMed] [Google Scholar]
- Cavaillon J. M., Udupa T. N., Chou C. T., Cinader B., Haeffner-Cavaillon N., Dubiski S. Rabbit B spleen lymphocytes and T helper cells. I. Responsiveness to mitogens of B cell subpopulations of different sedimentation velocities and subpopulations bearing or lacking Fcgamma receptors. J Immunol. 1979 Nov;123(5):2231–2238. [PubMed] [Google Scholar]
- Coutinho A., Möller G. Thymus-independent B-cell induction and paralysis. Adv Immunol. 1975;21:113–236. doi: 10.1016/s0065-2776(08)60220-5. [DOI] [PubMed] [Google Scholar]
- DeFranco A. L., Kung J. T., Paul W. E. Regulation of growth and proliferation in B cell subpopulations. Immunol Rev. 1982;64:161–182. doi: 10.1111/j.1600-065x.1982.tb00423.x. [DOI] [PubMed] [Google Scholar]
- Eskinazi D. P., Bessinger B. A., McNicholas J. M., Leary A. L., Knight K. L. Expression of an unidentified immunoglobulin isotype on rabbit Ig-bearing lymphocytes. J Immunol. 1979 Feb;122(2):469–474. [PubMed] [Google Scholar]
- Finkelman F. D., Lipsky P. E. The role of cell membrane immunoglobulin in primate B lymphocyte differentiation. Immunol Rev. 1979;45:117–139. doi: 10.1111/j.1600-065x.1979.tb00275.x. [DOI] [PubMed] [Google Scholar]
- Goding J. W. Conjugation of antibodies with fluorochromes: modifications to the standard methods. J Immunol Methods. 1976;13(3-4):215–226. doi: 10.1016/0022-1759(76)90068-5. [DOI] [PubMed] [Google Scholar]
- Gorczynski R. M., Feldmann M. B Cell heterogeneity - difference in the size of B lymphocytes responding to T dependent and T independent antigens. Cell Immunol. 1975 Jul;18(1):88–97. doi: 10.1016/0008-8749(75)90039-8. [DOI] [PubMed] [Google Scholar]
- Howard M., Farrar J., Hilfiker M., Johnson B., Takatsu K., Hamaoka T., Paul W. E. Identification of a T cell-derived b cell growth factor distinct from interleukin 2. J Exp Med. 1982 Mar 1;155(3):914–923. doi: 10.1084/jem.155.3.914. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Huber B., Gershon R. K., Cantor H. Identification of a B-cell surface structure involved in antigen-dependent triggering: absence of this structure on B cells from CBA/N mutant mice. J Exp Med. 1977 Jan 1;145(1):10–20. doi: 10.1084/jem.145.1.10. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Isakson P. C., Puré E., Vitetta E. S., Krammer P. H. T cell-derived B cell differentiation factor(s). Effect on the isotype switch of murine B cells. J Exp Med. 1982 Mar 1;155(3):734–748. doi: 10.1084/jem.155.3.734. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Keightley R. G., Cooper M. D., Lawton A. R. The T cell dependence of B cell differentiation induced by pokeweed mitogen. J Immunol. 1976 Nov;117(5 Pt 1):1538–1544. [PubMed] [Google Scholar]
- Kishimoto T., Ishizaka K. Regulation of antibody response in vitro. VI. Carrier-specific helper cells for IgG and IgE antibody response. J Immunol. 1973 Sep;111(3):720–732. [PubMed] [Google Scholar]
- Kulenkampff J., Janossy G., Greaves M. F. Acid esterase in human lymphoid cells and leukaemic blasts: a marker for T lymphocytes. Br J Haematol. 1977 Jun;36(2):231–240. doi: 10.1111/j.1365-2141.1977.tb00644.x. [DOI] [PubMed] [Google Scholar]
- L'age-Stehr J., Herzenberg L. A. Immunological memory in mice. I. Physical separation and partial characterization of memory cells for different immunoglobulin classes from each other and from antibody-producing cells. J Exp Med. 1970 Jun 1;131(6):1093–1108. doi: 10.1084/jem.131.6.1093. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Linthicum D. S., Sell S. Surface immunoglobulin on rabbit lymphoid cells. II. Ultrastructural distribution of b4 allotypic determinants and morphology of spleen lymphocytes. Cell Immunol. 1974 Jun;12(3):459–471. doi: 10.1016/0008-8749(74)90101-4. [DOI] [PubMed] [Google Scholar]
- Loken M. R. Separation of viable T and B lymphocytes using a cytochemical stain, Hoechst 33342. J Histochem Cytochem. 1980 Jan;28(1):36–39. doi: 10.1177/28.1.6153191. [DOI] [PubMed] [Google Scholar]
- Manconi P. E., Marrosu M. G., Paghi L., Correale G., Zaccheo D. Alpha-naphthyl acetate esterase activity in human lymphocytes: distribution in lymphocyte subpopulations and in mitogen-activated cells. Scand J Immunol. 1979;9(2):99–104. doi: 10.1111/j.1365-3083.1979.tb02711.x. [DOI] [PubMed] [Google Scholar]
- McNicholas J. M., Raffeld M., Loken M. R., Reiter H., Knight K. L. Monoclonal antibodies to rabbit lymphoid cells: preparation and characterization of a T-cell-specific antibody. Mol Immunol. 1981 Sep;18(9):815–822. doi: 10.1016/0161-5890(81)90003-1. [DOI] [PubMed] [Google Scholar]
- Mond J. J., Scher I., Cossman J., Kessler S., Mongini P. K., Hansen C., Finkelman F. D., Paul W. E. Role of the thymus in directing the development of a subset of B lymphocytes. J Exp Med. 1982 Mar 1;155(3):924–936. doi: 10.1084/jem.155.3.924. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mosier D. E., Scher I., Paul W. E. In vitro responses of CBA/N mice: spleen cells of mice with an X-linked defect that precludes immune responses to several thymus-independent antigens can respond to TNP-lipopolysaccharide. J Immunol. 1976 Oct;117(4):1363–1369. [PubMed] [Google Scholar]
- Shek P. N., Chou C. T., Dubiski S., Cinader B. Volume, adherence properties, membrane antigens and mitogen responsiveness of rabbit lymphoid cell subpopulations. Immunol Commun. 1975;4(1):81–93. doi: 10.3109/08820137509055763. [DOI] [PubMed] [Google Scholar]
- Teodorescu M., Mayer E. P., Reiter H., Dray S. Rabbit lymphocyte subpopulations. I. Separation of Ig+ and Ig- cells and their interaction in cultures stimulated by mitogens. Cell Immunol. 1976 Mar 1;22(1):66–75. doi: 10.1016/0008-8749(76)90007-1. [DOI] [PubMed] [Google Scholar]

