Induction of telomerase activity and maintenance of telomere length in virus-specific effector and memory CD8+ T cells

被引:41
作者
Hathcock, KS
Kaech, SM
Ahmed, R
Hodes, RJ
机构
[1] NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USA
[2] Emory Univ, Sch Med, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[4] NIA, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.4049/jimmunol.170.1.147
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Acute viral infections induce extensive proliferation and differentiation of virus-specific CD8(+) T cells. One mechanism reported to regulate the proliferative capacity of activated lymphocytes is mediated by the effect of telomerase in maintaining the length of telomeres in proliferating cells. We examined the regulation of telomerase activity and telomere length in naive CD8(+) T cells and in virus-specific CD8(+) T cells isolated from mice infected with lymphocytic choriomeningitis virus. These studies reveal that, compared with naive CD8(+) T cells, which express little or no telomerase activity, Ag-specific effector and long-lived memory CD8(+) T cells express high levels of telomerase activity. Despite the extensive clonal expansion that occurs during acute lymphocytic choriomeningitis virus infection, telomere length is maintained in both effector and memory CD8(+) T cells. These results suggest that induction of telomerase activity in Ag-specific effector and memory CD8(+) T cells is important for the extensive clonal expansion of both primary and secondary effector cells and for the maintenance and longevity of the memory CD8(+) T cell population.
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页码:147 / 152
页数:6
相关论文
共 29 条
[1]
SELECTION OF GENETIC-VARIANTS OF LYMPHOCYTIC CHORIOMENINGITIS VIRUS IN SPLEENS OF PERSISTENTLY INFECTED MICE - ROLE IN SUPPRESSION OF CYTO-TOXIC LYMPHOCYTE-T RESPONSE AND VIRAL PERSISTENCE [J].
AHMED, R ;
SALMI, A ;
BUTLER, LD ;
CHILLER, JM ;
OLDSTONE, MBA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (02) :521-540
[2]
Akbar AN, 2000, MECH AGEING DEV, V121, P69
[3]
EVIDENCE FOR A CRITICAL TELOMERE LENGTH IN SENESCENT HUMAN FIBROBLASTS [J].
ALLSOPP, RC ;
HARLEY, CB .
EXPERIMENTAL CELL RESEARCH, 1995, 219 (01) :130-136
[4]
Telomere shortening and tumor formation by mouse cells lacking telomerase RNA [J].
Blasco, MA ;
Lee, HW ;
Hande, MP ;
Samper, E ;
Lansdorp, PM ;
DePinho, RA ;
Greider, CW .
CELL, 1997, 91 (01) :25-34
[5]
Buchmeier M.J., 1999, PERSISTENT VIRAL INF, P575
[6]
TELOMERE LENGTH AND REPLICATIVE AGING IN HUMAN VASCULAR TISSUES [J].
CHANG, E ;
HARLEY, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (24) :11190-11194
[7]
Recruitment times, proliferation, and apoptosis rates during the CD8+ T-Cell response to lymphocytic choriomeningitis virus [J].
De Boer, RJ ;
Oprea, M ;
Antia, R ;
Murali-Krishna, K ;
Ahmed, R ;
Perelson, AS .
JOURNAL OF VIROLOGY, 2001, 75 (22) :10663-10669
[8]
Cutting edge: Increased expression of Bcl-2 in antigen-specific memory CD8+ T cells [J].
Grayson, JM ;
Zajac, AJ ;
Altman, JD ;
Ahmed, R .
JOURNAL OF IMMUNOLOGY, 2000, 164 (08) :3950-3954
[9]
Differentiating between memory and effector CD8 T cells by altered expression of cell surface O-glycans [J].
Harrington, LE ;
Galvan, M ;
Baum, LG ;
Altman, JD ;
Ahmed, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (07) :1241-1246
[10]
Hathcock KS, 1998, J IMMUNOL, V160, P5702