Senescence-related change in autologous mixed-lymphocyte reaction in senescence-accelerated mice

• Published in: Mechanisms of ageing and development Vol. 99; no. 1; pp. 19 - 32
• Main Authors: Kimura, S, Fukai, T, Morisaki, I, Daikoku, H, Hamada, S
• Format: Journal Article
• Language: English
• Published: Shannon Elsevier Ireland Ltd 01.12.1997; Elsevier Science
• Subjects: Aging - immunology; Animals; Autologous mixed-lymphocyte reaction; Biological and medical sciences; Fundamental and applied biological sciences. Psychology; Fundamental immunology; Immunobiology; Immunophenotyping; Kinetics; Mice; Mice, Inbred BALB C; Mice, Inbred Strains; Modulation of the immune response (stimulation, suppression); Murine T lymphocyte; Senescence-accelerated mice; Senescence-related change; Spleen - cytology; T-Lymphocyte Subsets - immunology; Time Factors; Senescence-accelerated mice; Senescence-related change; Murine T lymphocyte; Autologous mixed-lymphocyte reaction; Vertebrata; Senescence; Mammalia; Mixed lymphocyte reaction; Mouse; Rodentia; T-Lymphocyte; Immune regulation; Autologous system; Immune system
• ISSN: 0047-6374; 1872-6216
• DOI: 10.1016/S0047-6374(97)00085-7

Using the senescence-accelerated mouse (SAM) strains, we examined the senescence-related changes of autologous mixed-lymphocyte reaction (AMLR) as well as the phenotypic alteration of the T cell subsets. Splenic T cells from senescence-prone (SAM-P) and resistant (SAM-R) strains of mice were incubated with autologous non-T cells, and AMLR was measured on day 1–5. The kinetics of AMLR responses revealed a marked alteration in senescent SAM-P but not in non-senescent SAM-R mice, in which the peak response occurred at day 1, the response decreasing thereafter up to day 5. Similar senescence-related change was observed in aged (24-month-old) SAM-R and BALB/c mice. Furthermore, the T cells from the aged SAM-R mice cultured with non-senescent syngeneic non-T cells showed a very similar pattern to that cultured with autologous non-T cells. Flow cytometric analysis of T cell phenotype indicated that the percentage of CD4+CD45RBhi T cells correlated with the peak AMLR responses in both SAM-P and SAM-R mice, and that the percentage of the T cell subset with extrathymic properties was significantly higher in SAM-P mice. These findings suggest that the alteration in kinetics of AMLR is related to senescence but not to the strain of mice, and may reflect a senescence-related dysfunction of the autoregulatory immune mechanisms of T cells.