Abstract
The present report shows the capacity of hypothalamic extract (HE) to differentiate bone marrow cells to Thy-1+ cells in vitro. A two-step short-term culture was used. In the first step thymus and pituitary were co-cultured in the presence of HE. Supernatant was then transferred to a bone marrow cell suspension and following a period of culture, the percentage of Thy-1+ cells was determined by a microcytotoxicity assay. Results indicated that: (a) HE from young mice show a very efficient differentiating capacity; (b) HE from young mice is equally efficient when old pituitary, thymus and marrow are used; (c) HE from old donors has no capacity to differentiate T cells; (d) there is a progressive age-related decline of this capacity; and (e) there is a feed-back mechanism involved in this process. It is concluded that hypothalamic factors can regulate the differentiation of T cells and that this effect operates through a mechanism involving pituitary and thymus.
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Selected References
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- Arrenbrecht S. Specific binding of growth hormone to thymocytes. Nature. 1974 Nov 15;252(5480):255–257. doi: 10.1038/252255a0. [DOI] [PubMed] [Google Scholar]
- Bach J. F., Dardenne M. Studies on thymus products. II. Demonstration and characterization of a circulating thymic hormone. Immunology. 1973 Sep;25(3):353–366. [PMC free article] [PubMed] [Google Scholar]
- Bardos P., Bach J. F. Modulation of mouse natural killer cell activity by the serum thymic factor. Scand J Immunol. 1982 Oct;16(4):321–325. doi: 10.1111/j.1365-3083.1982.tb00730.x. [DOI] [PubMed] [Google Scholar]
- Blalock J. E. Production of neuroendocrine peptide hormones by the immune system. Prog Allergy. 1988;43:1–13. [PubMed] [Google Scholar]
- Bliznakov E. G., Wan Y. P., Chang D., Folkers K. Partial reactivation of impaired immune competence in aged mice by synthetic thymus factors. Biochem Biophys Res Commun. 1978 Feb 14;80(3):631–636. doi: 10.1016/0006-291x(78)91615-7. [DOI] [PubMed] [Google Scholar]
- Cross R. J., Markesbery W. R., Brooks W. H., Roszman T. L. Hypothalamic-immune interactions. I. The acute effect of anterior hypothalamic lesions on the immune response. Brain Res. 1980 Aug 25;196(1):79–87. doi: 10.1016/0006-8993(80)90717-9. [DOI] [PubMed] [Google Scholar]
- Dardenne M., Bach J. F. Studies on thymus products. I. Modification of rosette-forming cells by thymic extracts. Determination of the target RFC sub-population. Immunology. 1973 Sep;25(3):343–352. [PMC free article] [PubMed] [Google Scholar]
- Johnson H. M., Torres B. A. Immunoregulatory properties of neuroendocrine peptide hormones. Prog Allergy. 1988;43:37–67. [PubMed] [Google Scholar]
- Nagy E., Berczi I. Immunodeficiency in hypophysectomized rats. Acta Endocrinol (Copenh) 1978 Nov;89(3):530–537. doi: 10.1530/acta.0.0890530. [DOI] [PubMed] [Google Scholar]
- Prentice E. D., Lipscomb H., Metcalf W. K., Sharp J. G. Effects of hypophysectomy on DNCB-induced contact sensitivity in rats. Scand J Immunol. 1976;5(8):955–961. doi: 10.1111/j.1365-3083.1976.tb03047.x. [DOI] [PubMed] [Google Scholar]
- Russell D. H., Kibler R., Matrisian L., Larson D. F., Poulos B., Magun B. E. Prolactin receptors on human T and B lymphocytes: antagonism of prolactin binding by cyclosporine. J Immunol. 1985 May;134(5):3027–3031. [PubMed] [Google Scholar]
- SJODIN K., DALMASSO A. P., SMITH J. M., MARTINEZ C. THYMECTOMY IN NEWBORN AND ADULT MICE. Transplantation. 1963 Oct;1:521–525. doi: 10.1097/00007890-196301040-00011. [DOI] [PubMed] [Google Scholar]
- Savino W., Dardenne M., Papiernik M., Bach J. F. Thymic hormone-containing cells. Characterization and localization of serum thymic factor in young mouse thymus studied by monoclonal antibodies. J Exp Med. 1982 Aug 1;156(2):628–633. doi: 10.1084/jem.156.2.628. [DOI] [PMC free article] [PubMed] [Google Scholar]
