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Vitamin D(3) decreases TNF-α-induced inflammation in lung epithelial cells through a reduction in mitochondrial fission and mitophagy
Previous work has shown an association between vitamin D(3) deficiency and an increased risk for acquiring various inflammatory diseases. Vitamin D(3) can reduce morbidity and mortality in these patients via different mechanisms. Lung inflammation is an important event in the initiation and developm...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Netherlands
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275919/ https://www.ncbi.nlm.nih.gov/pubmed/34255241 http://dx.doi.org/10.1007/s10565-021-09629-6 |
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author | Chen, Yu-Chen Sung, Hsin-Ching Chuang, Tzu-Yi Lai, Tsai-Chun Lee, Tzu-Lin Lee, Chiang-Wen Lee, I.-Ta Chen, Yuh-Lien |
author_facet | Chen, Yu-Chen Sung, Hsin-Ching Chuang, Tzu-Yi Lai, Tsai-Chun Lee, Tzu-Lin Lee, Chiang-Wen Lee, I.-Ta Chen, Yuh-Lien |
author_sort | Chen, Yu-Chen |
collection | PubMed |
description | Previous work has shown an association between vitamin D(3) deficiency and an increased risk for acquiring various inflammatory diseases. Vitamin D(3) can reduce morbidity and mortality in these patients via different mechanisms. Lung inflammation is an important event in the initiation and development of respiratory disorders. However, the anti-inflammatory effects of vitamin D(3) and the underlying mechanisms remained to be determined. The purpose of this study was to examine the effects and mechanisms of action of vitamin D(3) (Vit. D) on the expression of intercellular adhesion molecule-1 (ICAM-1) in vitro and in vivo with or without tumor necrosis factor α (TNF-α) treatment. Pretreatment with Vit. D reduced the expression of ICAM-1 and leukocyte adhesion in TNF-α-treated A549 cells. TNF-α increased the accumulation of mitochondrial reactive oxygen species (mtROS), while Vit. D reduced this effect. Pretreatment with Vit. D attenuated TNF-α-induced mitochondrial fission, as shown by the increased expression of mitochondrial fission factor (Mff), phosphorylated dynamin-related protein 1 (p-DRP1), and mitophagy-related proteins (BCL2/adenovirus E1B 19 kDa protein-interacting protein 3, Bnip3) in A549 cells. Inhibition of DRP1 or Mff significantly decreased ICAM-1 expression. In addition, we found that Vit. D decreased TNF-α-induced ICAM-1 expression, mitochondrial fission, and mitophagy via the AKT and NF-κB pathways. Moreover, ICAM-1 expression, mitochondrial fission, and mitophagy were increased in the lung tissues of TNF-α-treated mice, while Vit. D supplementation reduced these effects. In this study, we elucidated the mechanisms by which Vit. D reduces the expression of adhesion molecules in models of airway inflammation. Vit. D might be served as a novel therapeutic agent for the targeting of epithelial activation in lung inflammation. GRAPHICAL ABSTRACT: [Image: see text] Graphical Headlights: • The expression of DRP1 and Mff, mitochondrial fission-related proteins, was increased in TNF-α-treated A549 cells. • The expression of Bnip3 and LC3B, mitophagy-related proteins, was increased in TNF-α-treated A549 cells. • Vit. D pretreatment decreased TNF-α-induced inflammation through the reduction of mitochondrial fission and mitophagy in A549 cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10565-021-09629-6. |
format | Online Article Text |
id | pubmed-8275919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-82759192021-07-14 Vitamin D(3) decreases TNF-α-induced inflammation in lung epithelial cells through a reduction in mitochondrial fission and mitophagy Chen, Yu-Chen Sung, Hsin-Ching Chuang, Tzu-Yi Lai, Tsai-Chun Lee, Tzu-Lin Lee, Chiang-Wen Lee, I.-Ta Chen, Yuh-Lien Cell Biol Toxicol Original Article Previous work has shown an association between vitamin D(3) deficiency and an increased risk for acquiring various inflammatory diseases. Vitamin D(3) can reduce morbidity and mortality in these patients via different mechanisms. Lung inflammation is an important event in the initiation and development of respiratory disorders. However, the anti-inflammatory effects of vitamin D(3) and the underlying mechanisms remained to be determined. The purpose of this study was to examine the effects and mechanisms of action of vitamin D(3) (Vit. D) on the expression of intercellular adhesion molecule-1 (ICAM-1) in vitro and in vivo with or without tumor necrosis factor α (TNF-α) treatment. Pretreatment with Vit. D reduced the expression of ICAM-1 and leukocyte adhesion in TNF-α-treated A549 cells. TNF-α increased the accumulation of mitochondrial reactive oxygen species (mtROS), while Vit. D reduced this effect. Pretreatment with Vit. D attenuated TNF-α-induced mitochondrial fission, as shown by the increased expression of mitochondrial fission factor (Mff), phosphorylated dynamin-related protein 1 (p-DRP1), and mitophagy-related proteins (BCL2/adenovirus E1B 19 kDa protein-interacting protein 3, Bnip3) in A549 cells. Inhibition of DRP1 or Mff significantly decreased ICAM-1 expression. In addition, we found that Vit. D decreased TNF-α-induced ICAM-1 expression, mitochondrial fission, and mitophagy via the AKT and NF-κB pathways. Moreover, ICAM-1 expression, mitochondrial fission, and mitophagy were increased in the lung tissues of TNF-α-treated mice, while Vit. D supplementation reduced these effects. In this study, we elucidated the mechanisms by which Vit. D reduces the expression of adhesion molecules in models of airway inflammation. Vit. D might be served as a novel therapeutic agent for the targeting of epithelial activation in lung inflammation. GRAPHICAL ABSTRACT: [Image: see text] Graphical Headlights: • The expression of DRP1 and Mff, mitochondrial fission-related proteins, was increased in TNF-α-treated A549 cells. • The expression of Bnip3 and LC3B, mitophagy-related proteins, was increased in TNF-α-treated A549 cells. • Vit. D pretreatment decreased TNF-α-induced inflammation through the reduction of mitochondrial fission and mitophagy in A549 cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10565-021-09629-6. Springer Netherlands 2021-07-13 2022 /pmc/articles/PMC8275919/ /pubmed/34255241 http://dx.doi.org/10.1007/s10565-021-09629-6 Text en © The Author(s), under exclusive licence to Springer Nature B.V. 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Chen, Yu-Chen Sung, Hsin-Ching Chuang, Tzu-Yi Lai, Tsai-Chun Lee, Tzu-Lin Lee, Chiang-Wen Lee, I.-Ta Chen, Yuh-Lien Vitamin D(3) decreases TNF-α-induced inflammation in lung epithelial cells through a reduction in mitochondrial fission and mitophagy |
title | Vitamin D(3) decreases TNF-α-induced inflammation in lung epithelial cells through a reduction in mitochondrial fission and mitophagy |
title_full | Vitamin D(3) decreases TNF-α-induced inflammation in lung epithelial cells through a reduction in mitochondrial fission and mitophagy |
title_fullStr | Vitamin D(3) decreases TNF-α-induced inflammation in lung epithelial cells through a reduction in mitochondrial fission and mitophagy |
title_full_unstemmed | Vitamin D(3) decreases TNF-α-induced inflammation in lung epithelial cells through a reduction in mitochondrial fission and mitophagy |
title_short | Vitamin D(3) decreases TNF-α-induced inflammation in lung epithelial cells through a reduction in mitochondrial fission and mitophagy |
title_sort | vitamin d(3) decreases tnf-α-induced inflammation in lung epithelial cells through a reduction in mitochondrial fission and mitophagy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8275919/ https://www.ncbi.nlm.nih.gov/pubmed/34255241 http://dx.doi.org/10.1007/s10565-021-09629-6 |
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