Abstract
The present studies have shown that cells capable of specific localization in response to challenge with CRBC or SRBC synthesize DNA very rapidly during the period from 2–5 days (peak 3 days) post primary immunization. This has been done by incubating the antigenically stimulated lymphoid cells with [3H] or [14C]thymidine in vitro for 45 min before adoptive transfer to syngeneic recipients. Specifically localizing cells (SLC) labeled in this way may ultimately account for up to 50% of the 3H or 14C present in a set of specifically challenged lymph nodes 3 days later. The data presented are consistent with the hypothesis that SLC numerically constitute only a very small fraction of the total number of recirculating lymphocytes trapped in antigenically stimulated lymph nodes, and that the demonstration of specific localization therefore depends upon selectively labeling these SLC relative to other recirculating cells. Attempts to selectively label the RNA of SLC with the precursor uridine have to date met with only very limited success.
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- Andersson J., Möller G., Sjöberg O. Selective induction of DNA synthesis in T and B lymphocytes. Cell Immunol. 1972 Aug;4(4):381–393. doi: 10.1016/0008-8749(72)90040-8. [DOI] [PubMed] [Google Scholar]
- COTTIER H., ODARTCHENKO N., KEISER G., HESS M., STONER R. D. INCORPORATION OF TRITIATED NUCLEOSIDES AND AMINO ACIDS INTO LYMPHOID AND PLASMOCYTOID CELLS DURING SECONDARY RESPONSE TO TETANUS TOXOID IN MICE. Ann N Y Acad Sci. 1964 Feb 28;113:612–626. doi: 10.1111/j.1749-6632.1964.tb40694.x. [DOI] [PubMed] [Google Scholar]
- DUTTON R. W., EADY J. D. AN IN VITRO SYSTEM FOR THE STUDY OF THE MECHANISM OF ANTIGENIC STIMULATION IN THE SECONDARY RESPONSE. Immunology. 1964 Jan;7:40–53. [PMC free article] [PubMed] [Google Scholar]
- DUTTON R. W. THE EFFECT OF ANTIGEN ON THE PROLIFERATION OF SPLEEN CELL SUSPENSIONS FROM TOLERANT RABBITS. J Immunol. 1964 Nov;93:814–815. [PubMed] [Google Scholar]
- Davies A. J., Leuchars E., Wallis V., Koller P. C. The mitotic response of thymus-derived cells to antigenic stimulus. Transplantation. 1966 Jul;4(4):438–451. doi: 10.1097/00007890-196607000-00008. [DOI] [PubMed] [Google Scholar]
- Delovitch T. L., Baglioni C. Estimation of light-chain gene reiteration of mouse immunoglobulin by DNA-RNA hybridization. Proc Natl Acad Sci U S A. 1973 Jan;70(1):173–178. doi: 10.1073/pnas.70.1.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dutton R. W., Mishell R. I. Cell populations and cell proliferation in the in vitro response of normal mouse spleen to heterologous erythrocytes. Analysis by the hot pulse technique. J Exp Med. 1967 Sep 1;126(3):443–454. doi: 10.1084/jem.126.3.443. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Elfenbein G. J., Shevach E. M., Green I. Proliferation by bone marrow-derived lymphocytes in response to antigenic stimulation in vitro. J Immunol. 1972 Oct;109(4):870–874. [PubMed] [Google Scholar]
- Emeson E. E., Thursh D. R. Immunologically specific retention of long-lived lymphoid cells in antigenically stimulated lymph nodes. J Immunol. 1971 Mar;106(3):635–643. [PubMed] [Google Scholar]
- Falkoff R., Kettman J. Differential stimulation of precursor cells and carrier-specific thymus-derived cell activity in the in vivo reponse to heterologous erythrocytes in mice. J Immunol. 1972 Jan;108(1):54–58. [PubMed] [Google Scholar]
- Feldmann M., Basten A. Cell interactions in the immune response in vitro. IV. Comparison of the effects of antigen-specific and allogeneic thymus-derived cell factors. J Exp Med. 1972 Oct 1;136(4):722–736. doi: 10.1084/jem.136.4.722. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GOWANS J. L., KNIGHT E. J. THE ROUTE OF RE-CIRCULATION OF LYMPHOCYTES IN THE RAT. Proc R Soc Lond B Biol Sci. 1964 Jan 14;159:257–282. doi: 10.1098/rspb.1964.0001. [DOI] [PubMed] [Google Scholar]
- Gery I., Krüger J., Spiesel S. Z. Stimulation of B-lymphocytes by endotoxin. Reactions of thymus-deprived mice and karyotypic analysis of dividing cells in mice bearing T 6 T 6 thymus grafts. J Immunol. 1972 Apr;108(4):1088–1091. [PubMed] [Google Scholar]
- Harris G. Antibody production in vitro. I. Single cell studies of the secondary response to sheep erythrocytes. J Exp Med. 1968 Apr 1;127(4):661–674. doi: 10.1084/jem.127.4.661. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Harris G., Pelc S. R. Incorporation of [3H] thymidine into the spleens of intact mice during the immune response to sheep erythrocytes (SRC). Immunology. 1970 Dec;19(6):865–878. [PMC free article] [PubMed] [Google Scholar]
- Hartmann K. U. Induction of a hemolysin response in vitro. Interaction of cells of bone marrow origin and thymic origin. J Exp Med. 1970 Dec 1;132(6):1267–1278. doi: 10.1084/jem.132.6.1267. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Howard J. C., Hunt S. V., Gowans J. L. Identification of marrow-derived and thymus-derived small lymphocytes in the lymphoid tissue and thoracic duct lymph of normal rats. J Exp Med. 1972 Feb 1;135(2):200–219. doi: 10.1084/jem.135.2.200. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ito T., Shearer G. M., Trizio D., Cudkowicz G. B cell activation in vivo by nonantigen-specific interaction with T cells. Frequency of immune responses increased by immunization with two antigens. J Exp Med. 1972 Aug 1;136(2):381–386. doi: 10.1084/jem.136.2.381. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jacobs R. P., Blaese R. M., Oppenheim J. J. Inhibition of antigen-stimulated in vitro proliferation of thymic dependent chicken spleen cells by specific antibody. J Immunol. 1972 Aug;109(2):324–333. [PubMed] [Google Scholar]
- Katz D. H., Osborne D. P., Jr The allogeneic effect in inbred mice. II. Establishment of the cellular interactions required for enhancement of antibody production by the graft-versus-host reaction. J Exp Med. 1972 Sep 1;136(3):455–465. doi: 10.1084/jem.136.3.455. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Krüger J., Gershon R. K. DNA synthetic response of thymocytes to a variety of antigens. J Immunol. 1972 Mar;108(3):581–585. [PubMed] [Google Scholar]
- MITCHELL J., MCDONALD W., NOSSAL G. J. AUTORADIOGRAPHIC STUDIES OF THE IMMUNE RESPONSE. 3. DIFFERENTIAL LYMPHOPOIESIS IN VARIOUS ORGANS. Aust J Exp Biol Med Sci. 1963 Aug;41:SUPPL411–SUPPL421. doi: 10.1038/icb.1963.62. [DOI] [PubMed] [Google Scholar]
- Miller H. C., Cudkowicz G. Antigen-specific cells in mouse bone marrow. I. Lasting effects of priming on immunocyte production by transferred marrow. J Exp Med. 1970 Dec 1;132(6):1122–1137. doi: 10.1084/jem.132.6.1122. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mond J. J., Takahashi T., Thorbecke G. J. Thymus-derived cell (T cell) activation by heterologous antigens as a replacement of specific immune T cells in the transfer of the secondary response to sheep erythrocytes. J Exp Med. 1972 Oct 1;136(4):715–721. doi: 10.1084/jem.136.4.715. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nordin A. A., Cosenza H., Sell S. Immunoglobulin classes of antibody-forming cells in mice. IV. The incorporation of tritiated thymidine into IgM and gamma 1 plaque-forming cells during the primary immune response. J Immunol. 1970 Jul;105(1):154–161. [PubMed] [Google Scholar]
- O'Brien T. F., Coons A. H. STUDIES ON ANTIBODY PRODUCTION : VII. THE EFFECT OF 5-BROMODEOXYURIDINE ON THE IN VITRO ANAMNESTIC ANTIBODY RESPONSE. J Exp Med. 1963 Jun 1;117(6):1063–1074. doi: 10.1084/jem.117.6.1063. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Paul W. E., Siskind G. W., Benacerraf B. Specificity of cellular immune responses. Antigen concentration dependence of stimulation of DNA synthesis in vitro by specifically sensitized cells, as an expression of the binding characteristics of cellular antibody. J Exp Med. 1968 Jan 1;127(1):25–42. doi: 10.1084/jem.127.1.25. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pelc S. R. Metabolic DNA in ciliated protozoa, salivary gland chromosomes, and mammalian cells. Int Rev Cytol. 1972;32:327–355. doi: 10.1016/s0074-7696(08)60344-7. [DOI] [PubMed] [Google Scholar]
- Piguet P. F., Vassalli P. Thymus-independent (B) cell proliferation in spleen cell cultures of mouse radiation chimeras stimulated by phytohemagglutinin or allogeneic cells. J Exp Med. 1972 Oct 1;136(4):962–967. doi: 10.1084/jem.136.4.962. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rubin A. S., Coons A. H. Specific heterologous enhancement of immune responses. 3. Partial characterization of supernatant material with enhancing activity. J Immunol. 1972 Jun;108(6):1597–1604. [PubMed] [Google Scholar]
- Saunders G. C. Maturation of hemolysin-producing cell clones. I. The kinetics of the induction period of an in vitro hemolysin response to erythrocyte antigen. J Exp Med. 1969 Sep 1;130(3):543–556. doi: 10.1084/jem.130.3.543. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Strober S. Initiation of antibody responses by different classes of lymphocytes. V. Fundamental changes in the physiological characteristics of virgin thymus-independent ("B") lymphocytes and "B" memory cells. J Exp Med. 1972 Oct 1;136(4):851–871. doi: 10.1084/jem.136.4.851. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thursh D. R., Emeson E. E. The immunologically specific retention of recirculating long-lived lymphocytes in lymph nodes stimulated by xenogeneic erythrocytes. J Exp Med. 1972 Apr 1;135(4):754–763. doi: 10.1084/jem.135.4.754. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WISSLER R. W., FITCH F. W., LA VIA M. F., GUNDERSON C. H. The cellular basis for antibody formation. J Cell Physiol Suppl. 1957 Dec;50(Suppl 1):265–301. doi: 10.1002/jcp.1030500417. [DOI] [PubMed] [Google Scholar]
- Werdelin O., Foley P. S., Rose N. R., McCluskey R. T. The growth of the cell population in the draining popliteal lymph node of rats injected with rat adrenal in Freund's Adjuvant. Immunology. 1971 Dec;21(6):1059–1063. [PMC free article] [PubMed] [Google Scholar]
- Wolstencroft R. A., Dumonde D. C. In vitro studies of cell-mediated immunity. I. Induction of lymphocyte transformation by a soluble "mitogenic" factor derived from interaction of sensitized guinea-pig lymphoid cells with specific antigen. Immunology. 1970 Apr;18(4):599–610. [PMC free article] [PubMed] [Google Scholar]