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Longitudinal Impact of WTC Dust Inhalation on Rat Cardiac Tissue Transcriptomic Profiles

First responders (FR) exposed to the World Trade Center (WTC) Ground Zero air over the first week after the 9/11 disaster have an increased heart disease incidence compared to unexposed FR and the general population. To test if WTC dusts were causative agents, rats were exposed to WTC dusts (under i...

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Autores principales: Park, Sung-Hyun, Lu, Yuting, Shao, Yongzhao, Prophete, Colette, Horton, Lori, Sisco, Maureen, Lee, Hyun-Wook, Kluz, Thomas, Sun, Hong, Costa, Max, Zelikoff, Judith, Chen, Lung-Chi, Gorr, Matthew W., Wold, Loren E., Cohen, Mitchell D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8776213/
https://www.ncbi.nlm.nih.gov/pubmed/35055737
http://dx.doi.org/10.3390/ijerph19020919
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author Park, Sung-Hyun
Lu, Yuting
Shao, Yongzhao
Prophete, Colette
Horton, Lori
Sisco, Maureen
Lee, Hyun-Wook
Kluz, Thomas
Sun, Hong
Costa, Max
Zelikoff, Judith
Chen, Lung-Chi
Gorr, Matthew W.
Wold, Loren E.
Cohen, Mitchell D.
author_facet Park, Sung-Hyun
Lu, Yuting
Shao, Yongzhao
Prophete, Colette
Horton, Lori
Sisco, Maureen
Lee, Hyun-Wook
Kluz, Thomas
Sun, Hong
Costa, Max
Zelikoff, Judith
Chen, Lung-Chi
Gorr, Matthew W.
Wold, Loren E.
Cohen, Mitchell D.
author_sort Park, Sung-Hyun
collection PubMed
description First responders (FR) exposed to the World Trade Center (WTC) Ground Zero air over the first week after the 9/11 disaster have an increased heart disease incidence compared to unexposed FR and the general population. To test if WTC dusts were causative agents, rats were exposed to WTC dusts (under isoflurane [ISO] anesthesia) 2 h/day on 2 consecutive days; controls received air/ISO or air only. Hearts were collected 1, 30, 240, and 360 d post-exposure, left ventricle total RNA was extracted, and transcription profiles were obtained. The data showed that differentially expressed genes (DEG) for WTC vs. ISO rats did not reach any significance with a false discovery rate (FDR) < 0.05 at days 1, 30, and 240, indicating that the dusts did not impart effects beyond any from ISO. However, at day 360, 14 DEG with a low FDR were identified, reflecting potential long-term effects from WTC dust alone, and the majority of these DEG have been implicated as having an impact on heart functions. Furthermore, the functional gene set enrichment analysis (GSEA) data at day 360 showed that WTC dust could potentially impact the myocardial energy metabolism via PPAR signaling and heart valve development. This is the first study showing that WTC dust could significantly affect some genes that are associated with the heart/CV system, in the long term. Even > 20 years after the 9/11 disaster, this has potentially important implications for those FR exposed repeatedly at Ground Zero over the first week after the buildings collapsed.
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spelling pubmed-87762132022-01-21 Longitudinal Impact of WTC Dust Inhalation on Rat Cardiac Tissue Transcriptomic Profiles Park, Sung-Hyun Lu, Yuting Shao, Yongzhao Prophete, Colette Horton, Lori Sisco, Maureen Lee, Hyun-Wook Kluz, Thomas Sun, Hong Costa, Max Zelikoff, Judith Chen, Lung-Chi Gorr, Matthew W. Wold, Loren E. Cohen, Mitchell D. Int J Environ Res Public Health Article First responders (FR) exposed to the World Trade Center (WTC) Ground Zero air over the first week after the 9/11 disaster have an increased heart disease incidence compared to unexposed FR and the general population. To test if WTC dusts were causative agents, rats were exposed to WTC dusts (under isoflurane [ISO] anesthesia) 2 h/day on 2 consecutive days; controls received air/ISO or air only. Hearts were collected 1, 30, 240, and 360 d post-exposure, left ventricle total RNA was extracted, and transcription profiles were obtained. The data showed that differentially expressed genes (DEG) for WTC vs. ISO rats did not reach any significance with a false discovery rate (FDR) < 0.05 at days 1, 30, and 240, indicating that the dusts did not impart effects beyond any from ISO. However, at day 360, 14 DEG with a low FDR were identified, reflecting potential long-term effects from WTC dust alone, and the majority of these DEG have been implicated as having an impact on heart functions. Furthermore, the functional gene set enrichment analysis (GSEA) data at day 360 showed that WTC dust could potentially impact the myocardial energy metabolism via PPAR signaling and heart valve development. This is the first study showing that WTC dust could significantly affect some genes that are associated with the heart/CV system, in the long term. Even > 20 years after the 9/11 disaster, this has potentially important implications for those FR exposed repeatedly at Ground Zero over the first week after the buildings collapsed. MDPI 2022-01-14 /pmc/articles/PMC8776213/ /pubmed/35055737 http://dx.doi.org/10.3390/ijerph19020919 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Park, Sung-Hyun
Lu, Yuting
Shao, Yongzhao
Prophete, Colette
Horton, Lori
Sisco, Maureen
Lee, Hyun-Wook
Kluz, Thomas
Sun, Hong
Costa, Max
Zelikoff, Judith
Chen, Lung-Chi
Gorr, Matthew W.
Wold, Loren E.
Cohen, Mitchell D.
Longitudinal Impact of WTC Dust Inhalation on Rat Cardiac Tissue Transcriptomic Profiles
title Longitudinal Impact of WTC Dust Inhalation on Rat Cardiac Tissue Transcriptomic Profiles
title_full Longitudinal Impact of WTC Dust Inhalation on Rat Cardiac Tissue Transcriptomic Profiles
title_fullStr Longitudinal Impact of WTC Dust Inhalation on Rat Cardiac Tissue Transcriptomic Profiles
title_full_unstemmed Longitudinal Impact of WTC Dust Inhalation on Rat Cardiac Tissue Transcriptomic Profiles
title_short Longitudinal Impact of WTC Dust Inhalation on Rat Cardiac Tissue Transcriptomic Profiles
title_sort longitudinal impact of wtc dust inhalation on rat cardiac tissue transcriptomic profiles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8776213/
https://www.ncbi.nlm.nih.gov/pubmed/35055737
http://dx.doi.org/10.3390/ijerph19020919
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