Literature DB >> 4927599

Some physical and radiobiological properties of immunologically reactive mouse spleen cells.

D Osoba.   

Abstract

Three classes of immunologically reactive cells, differing only slightly in size from each other, are required for the production of hemolysin-forming cells in culture. The three classes of cells can be detected in the normal mouse spleen by the combined use of rosette formation, velocity sedimentation, and irradiation. One class of cells (peak sedimentation velocity, 3.2 mm per hr) forms rosettes. The capacity of these cells to participate in immune responses to foreign erythrocytes is inhibited by relatively low doses of irradiation. These cells may be the immediate precursors of hemolysin-forming cells. A second class of cells (peak sedimentation velocity, 3.6 mm per hr) facilitates the production of hemolysin-forming cells by small numbers of normal spleen cells. Their facilitative activity is resistant to a relatively large dose of radiation. They do not form rosettes. The requirement of a third class of cells was deduced from the results of mixing experiments. Neither rosette-forming cells nor spleen cells largely depleted of rosette-forming cells could give rise to hemolysin-forming cells when cultured either alone or in the presence of large numbers of heavily irradiated cells. However, when rosette-forming cells, cells depleted of rosette-forming cells, and heavily irradiated cells were mixed together, hemolysin-forming cells were produced. The peak responses were found in fractions sedimenting at 4 mm per hr. Thus, it is suggested that these fractions contain a third class of cells. This class of cells does not form rosettes, but its function is inhibited by relatively low doses of radiation.

Entities:  

Mesh:

Substances:

Year:  1970        PMID: 4927599      PMCID: PMC2138742          DOI: 10.1084/jem.132.2.368

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


  12 in total

1.  A THREE-CELL INTERACTION REQUIRED FOR THE INDUCTION OF THE PRIMARY IMMUNE RESPONSE in vitro.

Authors:  D E Mosier; L W Coppleson
Journal:  Proc Natl Acad Sci U S A       Date:  1968-10       Impact factor: 11.205

2.  Primary immune response in cultures of spleen cells.

Authors:  J Marbrook
Journal:  Lancet       Date:  1967-12-16       Impact factor: 79.321

3.  Requirement of a nonproliferating class of cells for generation of immune responses in cell culture.

Authors:  J H Goldie; D Osoba
Journal:  Proc Soc Exp Biol Med       Date:  1970-04

4.  Rosette forming cells in non-immunized mice.

Authors:  R Laskov
Journal:  Nature       Date:  1968-08-31       Impact factor: 49.962

5.  Cellular deficit in thymectomized mice.

Authors:  D E Mosier; F W Fitch; D A Rowley; A J Davies
Journal:  Nature       Date:  1970-01-17       Impact factor: 49.962

6.  Membrane properties of living mammalian cells as studied by enzymatic hydrolysis of fluorogenic esters.

Authors:  B Rotman; B W Papermaster
Journal:  Proc Natl Acad Sci U S A       Date:  1966-01       Impact factor: 11.205

7.  X-ray resistant cell required for the induction of in vitro antibody formation.

Authors:  J Roseman
Journal:  Science       Date:  1969-09-12       Impact factor: 47.728

8.  Restriction of the capacity to respond to two antigens by single precursors of antibody-producing cells in culture.

Authors:  D Osoba
Journal:  J Exp Med       Date:  1969-01-01       Impact factor: 14.307

9.  Cell to cell interaction in the immune response. 3. Chromosomal marker analysis of single antibody-forming cells in reconstituted, irradiated, or thymectomized mice.

Authors:  G J Nossal; A Cunningham; G F Mitchell; J F Miller
Journal:  J Exp Med       Date:  1968-10-01       Impact factor: 14.307

10.  In vitro and in vivo studies of the immune response to sheep erythrocytes using partially purified cell preparations.

Authors:  J S Haskill; P Byrt; J Marbrook
Journal:  J Exp Med       Date:  1970-01-01       Impact factor: 14.307

View more
  19 in total

1.  The radiosensitivity of T and B lymphocytes in mice.

Authors:  Y Kataoka; T Sado
Journal:  Immunology       Date:  1975-07       Impact factor: 7.397

2.  Specific modulation of antibody production in vitro by soluble mediators.

Authors:  R M Gorczynski
Journal:  Immunology       Date:  1974-01       Impact factor: 7.397

3.  Different antibody responses to sheep and chicken red blood cells in mice.

Authors:  A Takada; Y Takada
Journal:  Immunology       Date:  1972-11       Impact factor: 7.397

4.  Restriction of specificity in the precursors of bone marrow-associated lymphocytes.

Authors:  L Lafleur; R G Miller; R A Phillips
Journal:  J Exp Med       Date:  1973-04-01       Impact factor: 14.307

5.  An in vivo primary response to 2,4,6-trinitrophenyl substituted erythrocytes.

Authors:  T L Pazdernik; E M Uyeki
Journal:  Immunology       Date:  1973-05       Impact factor: 7.397

6.  In vitro preferential effect of irradiation on cultured T lymphoid cell line.

Authors:  T Han; J L Pauly; J Minowada
Journal:  Clin Exp Immunol       Date:  1974-07       Impact factor: 4.330

7.  The functions of immune T and B rosette-forming cells.

Authors:  W Hall
Journal:  Immunology       Date:  1973-08       Impact factor: 7.397

8.  Antigenic characterization of murine rosette and plaque-forming cells.

Authors:  R Laskov; R Rabinowitz; M Schlesinger
Journal:  Immunology       Date:  1973-06       Impact factor: 7.397

9.  Thymus-derived rosettes are not "helper" cells.

Authors:  B E Elliott; J S Haskill; M A Axelrad
Journal:  J Exp Med       Date:  1973-11-01       Impact factor: 14.307

10.  Rosette-forming cells during immune response to Toxoplasma gondii in mice.

Authors:  K N Masihi; H Werner
Journal:  Infect Immun       Date:  1976-06       Impact factor: 3.441

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.