Differences in the Age-Dependent Release of a Low Molecular Weight Suppressor (LMWS) and Stimulators by Normal and NZB/W Lymphoid Organs

• Published in: The Journal of immunology (1950) Vol. 117; no. 4; pp. 1219 - 1225
• Main Authors: Ranney, David F, Steinberg, Alfred D
• Format: Journal Article
• Language: English
• Published: United States Am Assoc Immnol 01.10.1976
• Subjects: Aging; Animals; Cell-Free System; Dose-Response Relationship, Immunologic; Female; Immunosuppressive Agents - metabolism; Lymphoid Tissue - immunology; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Inbred NZB; Molecular Weight; Spleen - cytology; T-Lymphocytes - immunology
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.117.4.1219

The age-dependent release of soluble suppressors and stimulators of DNA synthesis by cultured thymocytes and spleen cells from C57BL/6 and BALB/c mice was compared with their release by NZB/W lymphoid organs. Spleen cells from the normal strains released high levels of suppressor early in life and gradually decresing quantities with age, NZB/W spleen cells exhibited an early deficiency followed by a later excess in the production of suppressor. These differences were quantitated by dose-response studies. Thymocytes from the normal strains released stimulatory factors throughout life. In contrast, NZB/W thymocytes stopped releasing stimulatory activity and began to produce suppressor after 2 1/2 to 4 months of life. This abnormal elaboration of suppressor by thymocytes occurred 2 months before its reappearance in the autologous spleen cell supernatant. Both the early and late-appearing (less than 1000). This activity was designed as low molecular weight suppressor (LMWS). Its aberrant production by their reported functional immunologic abnormalities. The following items were discussed: the production of LMWS by adherent spleen cells, its relationship to previously described regulators, its partial purification and initial chemical characterization, and exclusion of the naturally occurring inhibitors of lymphocyte activation, cortisol, corticosterone, cold thymidine, and cyclic AMP as the active molecule.