Aging affects the regeneration of the CD8(+) T cell compartment in bone marrow transplanted mice

Authors
Citation
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
Citations number
30
Categorie Soggetti
Cell & Developmental Biology
Journal title
MECHANISMS OF AGEING AND DEVELOPMENT
ISSN journal
00476374 → ACNP
Volume
112
Issue
2
Year of publication
2000
Pages
113 - 124
Database
ISI
SICI code
0047-6374(20000103)112:2<113:AATROT>2.0.ZU;2-O
Abstract
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.