Abstract
Corticosteroids suppress the humoral antibody response of mice to sheep erythrocytes. This response depends on interactions between thymus-derived helper cells and bone marrow-derived antibody-forming cell precursors (AFC precursors). Previous experiments had shown that spleen cells (a mixture of thymus-derived and marrow-derived cells) were sensitive to corticosteroids while AFC precursors in the bone marrow were resistant. The present experiments showed that the thymus of a mouse given 2.5 mg of hydrocortisone acetate, although containing only about 5% of the number of cells of a normal thymus, was as effective as a normal thymus in cooperating with bone marrow when transferred to irradiated syngeneic mice and stimulated with SRBC. The proliferative response of thymus helper cells to SRBC was also resistant to hydrocortisone. In this context, the majority of thymic cells are in the cortex, are rapidly dividing, are sensitive to corticosteroids and are not iminunocompetent. A small number of thymic cells, probably located in the medulla, are resistant to corticosteroids, but are immunocompetent since they can serve as helper cells. The hydrocortisone-sensitive phase of the splenic response to SRBC was found to be the bone marrow-derived AFC precursor since spleens from hydrocortisone-treated donors had immunocompetence restored by normal bone marrow but not by normal thymus cells.
Full Text
The Full Text of this article is available as a PDF (515.9 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Andersson B., Blomgren H. Evidence for a small pool of immunocompetent cells in the mouse thymus. Its role in the humoral antibody response against sheep erythrocytes, bovine serum albumin, ovalbumin and the NIP determinant. Cell Immunol. 1970 Oct;1(4):362–371. doi: 10.1016/0008-8749(70)90014-6. [DOI] [PubMed] [Google Scholar]
- BERGLUND K. Studies on factors which condition the effect of cortisone on antibody production. I. The significance of time of hormone administration in primary hemolysin response. Acta Pathol Microbiol Scand. 1956;38(4):311–328. doi: 10.1111/j.1699-0463.1956.tb01707.x. [DOI] [PubMed] [Google Scholar]
- Blomgren H., Andersson B. Evidence for a small pool of immunocompetent cells in the mouse thymus. Exp Cell Res. 1969 Oct;57(2):185–192. doi: 10.1016/0014-4827(69)90140-2. [DOI] [PubMed] [Google Scholar]
- Borum K. Pattern of cell production and cell migration in mouse thymus studied by autoradiography. Scand J Haematol. 1968;5(5):339–352. doi: 10.1111/j.1600-0609.1968.tb01758.x. [DOI] [PubMed] [Google Scholar]
- Brahim F., Osmond D. G. Migration of bone marrow lymphocytes demonstrated by selective bone marrow labeling with thymidine-H3. Anat Rec. 1970 Oct;168(2):139–159. doi: 10.1002/ar.1091680202. [DOI] [PubMed] [Google Scholar]
- Claman H. N., Chaperon E. A. Immunologic complementation between thymus and marrow cells--a model for the two-cell theory of immunocompetence. Transplant Rev. 1969;1:92–113. doi: 10.1111/j.1600-065x.1969.tb00137.x. [DOI] [PubMed] [Google Scholar]
- Cohen J. J., Fschbach M., Claman H. N. Hydrocortisne resistance of graft vs host activity in mouse thymus, spleen and bone marrow. J Immunol. 1970 Nov;105(5):1146–1150. [PubMed] [Google Scholar]
- Cohen J. J. Hydrocortisone resistance of activated initiator cells in graft versus host reactions. Nature. 1971 Jan 22;229(5282):274–275. doi: 10.1038/229274a0. [DOI] [PubMed] [Google Scholar]
- DOUGHERTY T. F. Effect of hormones on lympatic tissue. Physiol Rev. 1952 Oct;32(4):379–401. doi: 10.1152/physrev.1952.32.4.379. [DOI] [PubMed] [Google Scholar]
- ISHIDATE M., METCALF D. THE PATTERN OF LYMPHOPOIESIS IN THE MOUSE THYMUS AFTER CORTISONE ADMINISTRATION OR ADRENALECTOMY. Aust J Exp Biol Med Sci. 1963 Dec;41:637–649. doi: 10.1038/icb.1963.53. [DOI] [PubMed] [Google Scholar]
- Radovich J., Hemingsen H., Talmage D. W. The enhancing effect of bone marrow cells on the immune response of irradiated mice reconstituted with spleen cells from normal and immunized donors. J Immunol. 1968 Apr;100(4):756–759. [PubMed] [Google Scholar]
- SAINTE-MARIE G., LEBLOND C. P. CYTOLOGIC FEATURES AND CELLULAR MIGRATION IN THE CORTEX AND MEDULLA OF THYMUS IN THE YOUNG ADULT RAT. Blood. 1964 Mar;23:275–299. [PubMed] [Google Scholar]
- Schaumburg B. P., Bojesen E. Specificity and thermodynamic properties of the corticosteroid binding to a receptor of rat thymocytes in vitro. Biochim Biophys Acta. 1968 Nov 12;170(1):172–188. doi: 10.1016/0304-4165(68)90171-2. [DOI] [PubMed] [Google Scholar]
- Schlesinger M., Golakai V. K. Loss of thymus-distinctive serological characteristics in mice under certain conditions. Science. 1967 Mar 3;155(3766):1114–1116. doi: 10.1126/science.155.3766.1114. [DOI] [PubMed] [Google Scholar]
- Shortman K., Diener E., Russell P., Armstrong W. D. The role of nonlymphoid accessory cells in the immune response to different antigens. J Exp Med. 1970 Mar 1;131(3):461–482. doi: 10.1084/jem.131.3.461. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson J., van Furth R. The effect of glucocorticosteroids on the kinetics of mononuclear phagocytes. J Exp Med. 1970 Mar 1;131(3):429–442. doi: 10.1084/jem.131.3.429. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WARNER N. L. THE IMMUNOLOGICAL ROLE OF DIFFERENT LYMPHOID ORGANS IN THE CHICKEN. II. THE IMMUNOLOGICAL COMPETENCE OF THYMIC CELL SUSPENSIONS. Aust J Exp Biol Med Sci. 1964 Jun;42:401–416. doi: 10.1038/icb.1964.38. [DOI] [PubMed] [Google Scholar]
- Weber W. T. Difference between medullary and cortical thymic lymphocytes of the pig in their response to phytohemagglutinin. J Cell Physiol. 1966 Oct;68(2):117–125. doi: 10.1002/jcp.1040680206. [DOI] [PubMed] [Google Scholar]