Cargando…

Blood Cell Telomere Length Is a Dynamic Feature

There is a considerable heterogeneity in blood cell telomere length (TL) for individuals of similar age and recent studies have revealed that TL changes by time are dependent on TL at baseline. TL is partly inherited, but results from several studies indicate that e.g. life style and/or environmenta...

Descripción completa

Detalles Bibliográficos
Autores principales: Svenson, Ulrika, Nordfjäll, Katarina, Baird, Duncan, Roger, Laureline, Osterman, Pia, Hellenius, Mai-Lis, Roos, Göran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123359/
https://www.ncbi.nlm.nih.gov/pubmed/21720548
http://dx.doi.org/10.1371/journal.pone.0021485
_version_ 1782206977125908480
author Svenson, Ulrika
Nordfjäll, Katarina
Baird, Duncan
Roger, Laureline
Osterman, Pia
Hellenius, Mai-Lis
Roos, Göran
author_facet Svenson, Ulrika
Nordfjäll, Katarina
Baird, Duncan
Roger, Laureline
Osterman, Pia
Hellenius, Mai-Lis
Roos, Göran
author_sort Svenson, Ulrika
collection PubMed
description There is a considerable heterogeneity in blood cell telomere length (TL) for individuals of similar age and recent studies have revealed that TL changes by time are dependent on TL at baseline. TL is partly inherited, but results from several studies indicate that e.g. life style and/or environmental factors can affect TL during life. Collectively, these studies imply that blood cell TL might fluctuate during a life time and that the actual TL at a defined time point is the result of potential regulatory mechanism(s) and environmental factors. We analyzed relative TL (RTL) in subsequent blood samples taken six months apart from 50 individuals and found significant associations between RTL changes and RTL at baseline. Individual RTL changes per month were more pronounced than the changes recorded in a previously studied population analyzed after 10 years’ follow up. The data argues for an oscillating TL pattern which levels out at longer follow up times. In a separate group of five blood donors, a marked telomere loss was demonstrated within a six month period for one donor where after TL was stabilized. PCR determined RTL changes were verified by Southern blotting and STELA (single telomere elongation length analysis). The STELA demonstrated that for the donor with a marked telomere loss, the heterogeneity of the telomere distribution decreased considerably, with a noteworthy loss of the largest telomeres. In summary, the collected data support the concept that individual blood cell telomere length is a dynamic feature and this will be important to recognize in future studies of human telomere biology.
format Online
Article
Text
id pubmed-3123359
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-31233592011-06-29 Blood Cell Telomere Length Is a Dynamic Feature Svenson, Ulrika Nordfjäll, Katarina Baird, Duncan Roger, Laureline Osterman, Pia Hellenius, Mai-Lis Roos, Göran PLoS One Research Article There is a considerable heterogeneity in blood cell telomere length (TL) for individuals of similar age and recent studies have revealed that TL changes by time are dependent on TL at baseline. TL is partly inherited, but results from several studies indicate that e.g. life style and/or environmental factors can affect TL during life. Collectively, these studies imply that blood cell TL might fluctuate during a life time and that the actual TL at a defined time point is the result of potential regulatory mechanism(s) and environmental factors. We analyzed relative TL (RTL) in subsequent blood samples taken six months apart from 50 individuals and found significant associations between RTL changes and RTL at baseline. Individual RTL changes per month were more pronounced than the changes recorded in a previously studied population analyzed after 10 years’ follow up. The data argues for an oscillating TL pattern which levels out at longer follow up times. In a separate group of five blood donors, a marked telomere loss was demonstrated within a six month period for one donor where after TL was stabilized. PCR determined RTL changes were verified by Southern blotting and STELA (single telomere elongation length analysis). The STELA demonstrated that for the donor with a marked telomere loss, the heterogeneity of the telomere distribution decreased considerably, with a noteworthy loss of the largest telomeres. In summary, the collected data support the concept that individual blood cell telomere length is a dynamic feature and this will be important to recognize in future studies of human telomere biology. Public Library of Science 2011-06-24 /pmc/articles/PMC3123359/ /pubmed/21720548 http://dx.doi.org/10.1371/journal.pone.0021485 Text en Svenson et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Svenson, Ulrika
Nordfjäll, Katarina
Baird, Duncan
Roger, Laureline
Osterman, Pia
Hellenius, Mai-Lis
Roos, Göran
Blood Cell Telomere Length Is a Dynamic Feature
title Blood Cell Telomere Length Is a Dynamic Feature
title_full Blood Cell Telomere Length Is a Dynamic Feature
title_fullStr Blood Cell Telomere Length Is a Dynamic Feature
title_full_unstemmed Blood Cell Telomere Length Is a Dynamic Feature
title_short Blood Cell Telomere Length Is a Dynamic Feature
title_sort blood cell telomere length is a dynamic feature
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123359/
https://www.ncbi.nlm.nih.gov/pubmed/21720548
http://dx.doi.org/10.1371/journal.pone.0021485
work_keys_str_mv AT svensonulrika bloodcelltelomerelengthisadynamicfeature
AT nordfjallkatarina bloodcelltelomerelengthisadynamicfeature
AT bairdduncan bloodcelltelomerelengthisadynamicfeature
AT rogerlaureline bloodcelltelomerelengthisadynamicfeature
AT ostermanpia bloodcelltelomerelengthisadynamicfeature
AT helleniusmailis bloodcelltelomerelengthisadynamicfeature
AT roosgoran bloodcelltelomerelengthisadynamicfeature