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Silica inhalation altered telomere length and gene expression of telomere regulatory proteins in lung tissue of rats

Exposure to silica can cause lung fibrosis and cancer. Identification of molecular targets is important for the intervention and/or prevention of silica-induced lung diseases. Telomeres consist of tandem repeats of DNA sequences at the end of chromosomes, preventing chromosomal fusion and degradatio...

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Autores principales: Shoeb, Mohammad, Joseph, Pius, Kodali, Vamsi, Mustafa, Gul, Farris, Breanne Y., Umbright, Christina, Roberts, Jenny R., Erdely, Aaron, Antonini, James M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725592/
https://www.ncbi.nlm.nih.gov/pubmed/29230030
http://dx.doi.org/10.1038/s41598-017-17645-y
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author Shoeb, Mohammad
Joseph, Pius
Kodali, Vamsi
Mustafa, Gul
Farris, Breanne Y.
Umbright, Christina
Roberts, Jenny R.
Erdely, Aaron
Antonini, James M.
author_facet Shoeb, Mohammad
Joseph, Pius
Kodali, Vamsi
Mustafa, Gul
Farris, Breanne Y.
Umbright, Christina
Roberts, Jenny R.
Erdely, Aaron
Antonini, James M.
author_sort Shoeb, Mohammad
collection PubMed
description Exposure to silica can cause lung fibrosis and cancer. Identification of molecular targets is important for the intervention and/or prevention of silica-induced lung diseases. Telomeres consist of tandem repeats of DNA sequences at the end of chromosomes, preventing chromosomal fusion and degradation. Regulator of telomere length-1 (RTEL1) and telomerase reverse transcriptase (TERT), genes involved in telomere regulation and function, play important roles in maintaining telomere integrity and length. The goal of this study was to assess the effect of silica inhalation on telomere length and the regulation of RTEL1 and TERT. Lung tissues and blood samples were collected from rats at 4, 32, and 44 wk after exposure to 15 mg/m(3) of silica × 6 h/d × 5 d. Controls were exposed to air. At all-time points, RTEL1 expression was significantly decreased in lung tissue of the silica-exposed animals compared to controls. Also, significant increases in telomere length and TERT were observed in the silica group at 4 and 32 wk. Telomere length, RTEL1 and TERT expression may serve as potential biomarkers related to silica exposure and may offer insight into the molecular mechanism of silica-induced lung disease and tumorigeneses.
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spelling pubmed-57255922017-12-13 Silica inhalation altered telomere length and gene expression of telomere regulatory proteins in lung tissue of rats Shoeb, Mohammad Joseph, Pius Kodali, Vamsi Mustafa, Gul Farris, Breanne Y. Umbright, Christina Roberts, Jenny R. Erdely, Aaron Antonini, James M. Sci Rep Article Exposure to silica can cause lung fibrosis and cancer. Identification of molecular targets is important for the intervention and/or prevention of silica-induced lung diseases. Telomeres consist of tandem repeats of DNA sequences at the end of chromosomes, preventing chromosomal fusion and degradation. Regulator of telomere length-1 (RTEL1) and telomerase reverse transcriptase (TERT), genes involved in telomere regulation and function, play important roles in maintaining telomere integrity and length. The goal of this study was to assess the effect of silica inhalation on telomere length and the regulation of RTEL1 and TERT. Lung tissues and blood samples were collected from rats at 4, 32, and 44 wk after exposure to 15 mg/m(3) of silica × 6 h/d × 5 d. Controls were exposed to air. At all-time points, RTEL1 expression was significantly decreased in lung tissue of the silica-exposed animals compared to controls. Also, significant increases in telomere length and TERT were observed in the silica group at 4 and 32 wk. Telomere length, RTEL1 and TERT expression may serve as potential biomarkers related to silica exposure and may offer insight into the molecular mechanism of silica-induced lung disease and tumorigeneses. Nature Publishing Group UK 2017-12-11 /pmc/articles/PMC5725592/ /pubmed/29230030 http://dx.doi.org/10.1038/s41598-017-17645-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shoeb, Mohammad
Joseph, Pius
Kodali, Vamsi
Mustafa, Gul
Farris, Breanne Y.
Umbright, Christina
Roberts, Jenny R.
Erdely, Aaron
Antonini, James M.
Silica inhalation altered telomere length and gene expression of telomere regulatory proteins in lung tissue of rats
title Silica inhalation altered telomere length and gene expression of telomere regulatory proteins in lung tissue of rats
title_full Silica inhalation altered telomere length and gene expression of telomere regulatory proteins in lung tissue of rats
title_fullStr Silica inhalation altered telomere length and gene expression of telomere regulatory proteins in lung tissue of rats
title_full_unstemmed Silica inhalation altered telomere length and gene expression of telomere regulatory proteins in lung tissue of rats
title_short Silica inhalation altered telomere length and gene expression of telomere regulatory proteins in lung tissue of rats
title_sort silica inhalation altered telomere length and gene expression of telomere regulatory proteins in lung tissue of rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725592/
https://www.ncbi.nlm.nih.gov/pubmed/29230030
http://dx.doi.org/10.1038/s41598-017-17645-y
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