Lymphocyte aging in bone marrow chimeras.

Chimeric mice provide a unique approach to the analysis of genetic factors associated with aging since cells with two genetically distinct backgrounds can be analyzed in the same animal. In this study, bone marrow chimeras were produced by reconstituting lethally irradiated female B6AF1 [(C57BL/6 female x A male)F1] mice with varying mixtures of T cell-depleted bone marrow cells from A (short-lived) and C57BL/6 (long-lived) mice. The phenotypic composition of the peripheral blood lymphocytes was analyzed using either a cytotoxicity assay or flow cytometry with indirect immunofluorescence. The percentage of A-derived lymphocytes in the peripheral blood following reconstitution was generally higher than the percentage of A bone marrow cells with which the irradiated mice were inoculated, suggesting that the cells from the A donor bone marrow were more efficient at marrow reconstitution than the cells from the C57BL/6 donor bone marrow. In order to determine whether the percentage of A- versus C57BL/6-derived cells changed with age in each animal, the chimeric mice were bled for phenotype analysis of peripheral blood lymphocytes between 2-6 months following reconstitution and at 2-3 month intervals until death. For most animals [93/127 (73%)], there was no consistent pattern of increase or decrease (> 20%) with regard to the percentage of A lymphocytes in the peripheral blood over time. However, in 34/127 (27%) of the chimeras, a change greater than 20% in the phenotypic composition of the peripheral blood lymphocytes was observed and these animals were considered unstable. Among these 34 unstable animals, 6 (18%) showed an overall increase in A-derived lymphocytes, 24 (71%) showed an overall decrease in A-derived lymphocytes, and 4 (12%) showed fluctuating increases and decreases over their lifespan. While the lifespans of the chimeric animals in these studies were considerably shorter than those reported for untreated mice of the same strain and gender, in these animals increased proportions of A cells were associated with significantly longer lifespans. In addition, the lifespan of the B6AF1 chimeric mice was a function of the proportion of A lymphocytes present in the peripheral blood over the course of the animal's life.