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Organic dust inhibits surfactant protein expression by reducing thyroid transcription factor-1 levels in human lung epithelial cells
Exposure to organic dust is a risk factor for the development of respiratory diseases. Surfactant proteins (SP) reduce alveolar surface tension and modulate innate immune responses to control lung inflammation. Therefore, changes in SP levels could contribute to the development of organic-dust-induc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830861/ https://www.ncbi.nlm.nih.gov/pubmed/30774012 http://dx.doi.org/10.1177/1753425919827360 |
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author | Natarajan, Kartiga Gangam, Keerthi Meganathan, Velmurugan Gottipati, Koteswara R Mitchell, Courtney Boggaram, Vijay |
author_facet | Natarajan, Kartiga Gangam, Keerthi Meganathan, Velmurugan Gottipati, Koteswara R Mitchell, Courtney Boggaram, Vijay |
author_sort | Natarajan, Kartiga |
collection | PubMed |
description | Exposure to organic dust is a risk factor for the development of respiratory diseases. Surfactant proteins (SP) reduce alveolar surface tension and modulate innate immune responses to control lung inflammation. Therefore, changes in SP levels could contribute to the development of organic-dust-induced respiratory diseases. Because information on the effects of organic dust on SP levels is lacking, we studied the effects of dust from a poultry farm on SP expression. We found that dust extract reduced SP-A and SP-B mRNA and protein levels in H441 human lung epithelial cells by inhibiting their promoter activities, but did not have any effect on SP-D protein levels. Dust extract also reduced SP-A and SP-C levels in primary human alveolar epithelial cells. The inhibitory effects were not due to LPS or protease activities present in dust extract or mediated via oxidative stress, but were dependent on a heat-labile factor(s). Thyroid transcription factor-1, a key transcriptional activator of SP expression, was reduced in dust-extract-treated cells, indicating that its down-regulation mediates inhibition of SP levels. Our study implies that down-regulation of SP levels by organic dust could contribute to the development of lung inflammation and respiratory diseases in humans. |
format | Online Article Text |
id | pubmed-6830861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-68308612019-11-20 Organic dust inhibits surfactant protein expression by reducing thyroid transcription factor-1 levels in human lung epithelial cells Natarajan, Kartiga Gangam, Keerthi Meganathan, Velmurugan Gottipati, Koteswara R Mitchell, Courtney Boggaram, Vijay Innate Immun Original Articles Exposure to organic dust is a risk factor for the development of respiratory diseases. Surfactant proteins (SP) reduce alveolar surface tension and modulate innate immune responses to control lung inflammation. Therefore, changes in SP levels could contribute to the development of organic-dust-induced respiratory diseases. Because information on the effects of organic dust on SP levels is lacking, we studied the effects of dust from a poultry farm on SP expression. We found that dust extract reduced SP-A and SP-B mRNA and protein levels in H441 human lung epithelial cells by inhibiting their promoter activities, but did not have any effect on SP-D protein levels. Dust extract also reduced SP-A and SP-C levels in primary human alveolar epithelial cells. The inhibitory effects were not due to LPS or protease activities present in dust extract or mediated via oxidative stress, but were dependent on a heat-labile factor(s). Thyroid transcription factor-1, a key transcriptional activator of SP expression, was reduced in dust-extract-treated cells, indicating that its down-regulation mediates inhibition of SP levels. Our study implies that down-regulation of SP levels by organic dust could contribute to the development of lung inflammation and respiratory diseases in humans. SAGE Publications 2019-02-06 2019-02 /pmc/articles/PMC6830861/ /pubmed/30774012 http://dx.doi.org/10.1177/1753425919827360 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Natarajan, Kartiga Gangam, Keerthi Meganathan, Velmurugan Gottipati, Koteswara R Mitchell, Courtney Boggaram, Vijay Organic dust inhibits surfactant protein expression by reducing thyroid transcription factor-1 levels in human lung epithelial cells |
title | Organic dust inhibits surfactant protein expression by reducing
thyroid transcription factor-1 levels in human lung epithelial
cells |
title_full | Organic dust inhibits surfactant protein expression by reducing
thyroid transcription factor-1 levels in human lung epithelial
cells |
title_fullStr | Organic dust inhibits surfactant protein expression by reducing
thyroid transcription factor-1 levels in human lung epithelial
cells |
title_full_unstemmed | Organic dust inhibits surfactant protein expression by reducing
thyroid transcription factor-1 levels in human lung epithelial
cells |
title_short | Organic dust inhibits surfactant protein expression by reducing
thyroid transcription factor-1 levels in human lung epithelial
cells |
title_sort | organic dust inhibits surfactant protein expression by reducing
thyroid transcription factor-1 levels in human lung epithelial
cells |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830861/ https://www.ncbi.nlm.nih.gov/pubmed/30774012 http://dx.doi.org/10.1177/1753425919827360 |
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