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

被引:11
作者
Mu, XY [1 ]
Thoman, ML [1 ]
机构
[1] Sidney Kimmel Canc Ctr, Dept Immunol, San Diego, CA 92121 USA
关键词
chimeric mice; aging; cytokines; differentiation;
D O I
10.1016/S0047-6374(99)00078-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A chimeric mouse model has been used to determine the effect of aging on the differentiation of CD8(+) T cells and on the regeneration capacity of the mature peripheral T cell pool after radiation induced depletion. Bone marrow cells from Thy 1.1(+) mice were transplanted into lethally irradiated young or aged mice (Thy 1.2(+)). After 6 weeks, splenic CD8(+) T cells were subjected 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 recipients, 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 mice, 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 the 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 < 0.01), suggesting that a significant over expansion of the Thy 1.2(+) CD8(+) subset occurred in young mice during regeneration. The Thy 1.1(+) CD8(+) T cells that developed in young hosts were of a naive phenotype with a majority of cells expressing a low level of CD44. In contrast, the majority of those 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 and IFN-gamma by Thy 1.1(+) CD8(+) T cells was affected by the age of the host. 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 influences the regeneration capacity of CD8(+) T cells. (C) 2000 Published by Elsevier Science Ireland Ltd. AII rights reserved.
引用
收藏
页码:113 / 124
页数:12
相关论文
共 30 条
[1]   Cellular interactions in thymocyte development [J].
Anderson, G ;
Moore, NC ;
Owen, JJT ;
Jenkinson, EJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :73-99
[2]  
BELL EB, 1987, J IMMUNOL, V139, P1379
[3]   The role of the thymus and recent thymic migrants in the maintenance of the adult peripheral lymphocyte pool [J].
Berzins, SP ;
Boyd, RL ;
Miller, JFAP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (11) :1839-1848
[4]   IS T-CELL MEMORY MAINTAINED BY CROSS-REACTIVE STIMULATION [J].
BEVERLEY, PCL .
IMMUNOLOGY TODAY, 1990, 11 (06) :203-205
[5]  
Engwerda CR, 1996, J IMMUNOL, V156, P3621
[6]   CELL-PROLIFERATION AND CYTOKINE PRODUCTION BY CD4+ CELLS FROM OLD MICE [J].
HOBBS, MV ;
ERNST, DN ;
TORBETT, BE ;
GLASEBROOK, AL ;
REHSE, MA ;
MCQUITTY, DN ;
THOMAN, ML ;
BOTTOMLY, K ;
ROTHERMEL, AL ;
NOONAN, DJ ;
WEIGLE, WO .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1991, 46 (04) :312-320
[7]  
HOBBS MV, 1993, J IMMUNOL, V150, P3602
[8]  
HOBBS MV, 1994, HUMAN CYTOKINES, P355
[9]   SEX-HORMONES AS NEGATIVE REGULATORS OF LYMPHOPOIESIS [J].
KINCADE, PW ;
MEDINA, KL ;
SMITHSON, G .
IMMUNOLOGICAL REVIEWS, 1994, 137 :119-134
[10]   POLYMORPHISM OF AGE-RELATED-CHANGES IN INTERLEUKIN (IL) PRODUCTION - DIFFERENTIAL CHANGES OF T HELPER SUBPOPULATIONS, SYNTHESIZING IL2, IL3 AND IL4 [J].
KUBO, M ;
CINADER, B .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (06) :1289-1296