Cutting edge: Antigen-dependent regulation of telomerase activity in murine T cells

被引:0
作者
Hathcock, KS
Weng, NP
Merica, R
Jenkins, MK
Hodes, R
机构
[1] NIA, NIH, Bethesda, MD 20892 USA
[2] NCI, Expt Immunol Branch, Bethesda, MD 20892 USA
[3] Univ Minnesota, Dept Microbiol, Ctr Immunol, Minneapolis, MN 55455 USA
关键词
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Telomeres, structures on the ends of linear chromosomes, function to maintain chromosomal integrity, Telomere shortening occurs with cell division and provides a mechanism for limiting the replicative potential of normal human somatic cells. Telomerase, a ribonucleoprotein enzyme, synthesizes telomeric repeats on chromosomal termini, potentially extending the capacity for cell division. The present study demonstrates that resting T cells express little/no activity, and optimal Ag-specific induction of telomerase activity in vitro requires both TCR and CD28-B7 costimulatory signals. Regulation of telomerase in T cells during in vivo Ag-dependent activation was also assessed by adoptive transfer of TCR transgenic T cells and subsequent Ag challenge. Under these conditions, telomerase was induced in transgenic T cells coincident with a phase of extensive clonal expansion, These findings suggest that telomerase may represent an adoptive response that functions to preserve replicative potential in Ag-reactive lymphocytes.
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页码:5702 / 5706
页数:5
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