Systematic and Cell Type-Specific Telomere Length Changes in Subsets of Lymphocytes
Systematic and Cell Type-Specific Telomere Length Changes in Subsets of Lymphocytes
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DOI:
10.1155/2016/5371050
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发表时间:
2016-01-01
影响因子:
4.1
通讯作者:
Blackburn, Elizabeth H.
中科院分区:
文献类型:
--
作者:
Lin, Jue;Cheon, Joshua;Blackburn, Elizabeth H.
Telomeres, the protective DNA-protein complexes at the ends of linear chromosomes, are important for genome stability. Leukocyte or peripheral blood mononuclear cell (PBMC) telomere length is a potential biomarker for human aging that integrates genetic, environmental, and lifestyle factors and is associated with mortality and risks for major diseases. However, only a limited number of studies have examined longitudinal changes of telomere length and few have reported data on sorted circulating immune cells. We examined the average telomere length (TL) in CD4+, CD8+CD28+, and CD8+CD28- T cells, B cells, and PBMCs, cross-sectionally and longitudinally, in a cohort of premenopausal women. We report that TL changes over 18 months were correlated among these three T cell types within the same participant. Additionally, PBMC TL change was also correlated with those of all three T cell types, and B cells. The rate of shortening for B cells was significantly greater than for the three T cell types. CD8+CD28- cells, despite having the shortest TL, showed significantly more rapid attrition when compared to CD8+CD28+ T cells. These results suggest systematically coordinated, yet cell type-specific responses to factors and pathways contribute to telomere length regulation.