Xy. Mu et Ml. Thoman, Aging affects the regeneration of the CD8(+) T cell compartment in bone marrow transplanted mice, MECH AGE D, 112(2), 2000, pp. 113-124
A chimeric mouse model has been used to determine the effect of aging on th
e differentiation of CD8(+) T cells and on the regeneration capacity of the
mature peripheral T cell pool after radiation induced depletion. Bone marr
ow cells from Thy 1.1(+) mice were transplanted into lethally irradiated yo
ung or aged mice (Thy 1.2(+)). After 6 weeks, splenic CD8(+) T cells were s
ubjected to phenotypic and functional examinations by flow cytometry. Both
young and aged mice were able to develop donor derived (Thy 1.1(+)) CD8(+)
T cells. Although the absolute number of T cells was reduced in aged recipi
ents, the ratio of CD4(+) to CD8(+) T cells of donor-origin was the same in
young Thy 1.1(+) control mice as it was in both young and aged chimeric mi
ce, indicating that aging has no effect on the ratio of CD4(+) to CD8(+) T
cells produced by the thymus. However, the percentage of CD8(+) cells in th
e total Thy 1.2(+) (host-origin)T cell population was significantly higher
in young chimeric mice than in age-matched Thy 1.2(+) control mice (P < 0.0
1), suggesting that a significant over expansion of the Thy 1.2(+) CD8(+) s
ubset occurred in young mice during regeneration. The Thy 1.1(+) CD8(+) T c
ells that developed in young hosts were of a naive phenotype with a majorit
y of cells expressing a low level of CD44. In contrast, the majority of tho
se that developed in the aged host displayed a memory phenotype with a high
percentage of cells being CD44(hi). In addition, the production of IL-4 an
d IFN-gamma by Thy 1.1(+) CD8(+) T cells was affected by the age of the hos
t. A greater fraction of aged Thy 1.1(+) CD8(+) T cells could be induced to
produce either IFN-gamma or IL-4 than young CD8(+) T cells. These results
suggested that the aged microenvironment has a significant effect on newly
developed CD8(+) T cells and that the age of the microenvironment also infl
uences the regeneration capacity of CD8(+) T cells. (C) 2000 Published by E
lsevier Science Ireland Ltd. AII rights reserved.