Systematic and Cell Type-Specific Telomere Length Changes in Subsets of Lymphocytes

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 a...

Full description

Saved in:
Bibliographic Details
Main Authors: Jue Lin, Joshua Cheon, Rashida Brown, Michael Coccia, Eli Puterman, Kirstin Aschbacher, Elizabeth Sinclair, Elissa Epel, Elizabeth H. Blackburn
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2016/5371050
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832566671981674496
author Jue Lin
Joshua Cheon
Rashida Brown
Michael Coccia
Eli Puterman
Kirstin Aschbacher
Elizabeth Sinclair
Elissa Epel
Elizabeth H. Blackburn
author_facet Jue Lin
Joshua Cheon
Rashida Brown
Michael Coccia
Eli Puterman
Kirstin Aschbacher
Elizabeth Sinclair
Elissa Epel
Elizabeth H. Blackburn
author_sort Jue Lin
collection DOAJ
description 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.
format Article
id doaj-art-48a1f1ef7877424287eef9edd47c545b
institution Kabale University
issn 2314-8861
2314-7156
language English
publishDate 2016-01-01
publisher Wiley
record_format Article
series Journal of Immunology Research
spelling doaj-art-48a1f1ef7877424287eef9edd47c545b2025-02-03T01:03:28ZengWileyJournal of Immunology Research2314-88612314-71562016-01-01201610.1155/2016/53710505371050Systematic and Cell Type-Specific Telomere Length Changes in Subsets of LymphocytesJue Lin0Joshua Cheon1Rashida Brown2Michael Coccia3Eli Puterman4Kirstin Aschbacher5Elizabeth Sinclair6Elissa Epel7Elizabeth H. Blackburn8Department of Biochemistry and Biophysics, University of California San Francisco, San Francisco, CA 94143, USADepartment of Biochemistry and Biophysics, University of California San Francisco, San Francisco, CA 94143, USADivision of Epidemiology, University of California Berkeley, Berkeley, CA 94720, USADepartment of Psychiatry, University of California San Francisco, San Francisco, CA 94118, USASchool of Kinesiology, University of British Columbia, Vancouver, BC, V6T 1Z1, CanadaDepartment of Psychiatry, University of California San Francisco, San Francisco, CA 94118, USACore Immunology Lab, Division of Experimental Medicine, University of California San Francisco, San Francisco, CA 94110, USADepartment of Psychiatry, University of California San Francisco, San Francisco, CA 94118, USADepartment of Biochemistry and Biophysics, University of California San Francisco, San Francisco, CA 94143, USATelomeres, 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.http://dx.doi.org/10.1155/2016/5371050
spellingShingle Jue Lin
Joshua Cheon
Rashida Brown
Michael Coccia
Eli Puterman
Kirstin Aschbacher
Elizabeth Sinclair
Elissa Epel
Elizabeth H. Blackburn
Systematic and Cell Type-Specific Telomere Length Changes in Subsets of Lymphocytes
Journal of Immunology Research
title Systematic and Cell Type-Specific Telomere Length Changes in Subsets of Lymphocytes
title_full Systematic and Cell Type-Specific Telomere Length Changes in Subsets of Lymphocytes
title_fullStr Systematic and Cell Type-Specific Telomere Length Changes in Subsets of Lymphocytes
title_full_unstemmed Systematic and Cell Type-Specific Telomere Length Changes in Subsets of Lymphocytes
title_short Systematic and Cell Type-Specific Telomere Length Changes in Subsets of Lymphocytes
title_sort systematic and cell type specific telomere length changes in subsets of lymphocytes
url http://dx.doi.org/10.1155/2016/5371050
work_keys_str_mv AT juelin systematicandcelltypespecifictelomerelengthchangesinsubsetsoflymphocytes
AT joshuacheon systematicandcelltypespecifictelomerelengthchangesinsubsetsoflymphocytes
AT rashidabrown systematicandcelltypespecifictelomerelengthchangesinsubsetsoflymphocytes
AT michaelcoccia systematicandcelltypespecifictelomerelengthchangesinsubsetsoflymphocytes
AT eliputerman systematicandcelltypespecifictelomerelengthchangesinsubsetsoflymphocytes
AT kirstinaschbacher systematicandcelltypespecifictelomerelengthchangesinsubsetsoflymphocytes
AT elizabethsinclair systematicandcelltypespecifictelomerelengthchangesinsubsetsoflymphocytes
AT elissaepel systematicandcelltypespecifictelomerelengthchangesinsubsetsoflymphocytes
AT elizabethhblackburn systematicandcelltypespecifictelomerelengthchangesinsubsetsoflymphocytes