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TIFA protein expression is associated with pulmonary arterial hypertension
Tumor necrosis factor receptor-associated factor-interacting protein with a forkhead-associated domain (TIFA), a key regulator of inflammation, may be involved in the pathogenesis of pulmonary arterial hypertension (PAH). A total of 48 PAH patients (age 50.1 ± 13.1 years, 22.9% men), 25 hypertensive...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266829/ https://www.ncbi.nlm.nih.gov/pubmed/34238983 http://dx.doi.org/10.1038/s41598-021-93582-1 |
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author | Chang, Hao-Chih Wei, Tong-You Wade Wu, Pei-Yu Tsai, Ming-Daw Yu, Wen-Chung Chen, Chen-Huan Sung, Shih-Hsien |
author_facet | Chang, Hao-Chih Wei, Tong-You Wade Wu, Pei-Yu Tsai, Ming-Daw Yu, Wen-Chung Chen, Chen-Huan Sung, Shih-Hsien |
author_sort | Chang, Hao-Chih |
collection | PubMed |
description | Tumor necrosis factor receptor-associated factor-interacting protein with a forkhead-associated domain (TIFA), a key regulator of inflammation, may be involved in the pathogenesis of pulmonary arterial hypertension (PAH). A total of 48 PAH patients (age 50.1 ± 13.1 years, 22.9% men), 25 hypertensive subjects, and 26 healthy controls were enrolled. TIFA protein expression in peripheral blood mononuclear cells (PBMCs) and plasma interleukin (IL)-1β and tumor necrosis factor (TNF)-α were measured. Pulmonary arterial hemodynamics were derived from right heart catheterization. PAH patients had the highest expression of TIFA, TNF-α, and IL-1β. TIFA protein expression was significantly associated with IL-1β (r = 0.94; P < 0.001), TNF-α (r = 0.93; P < 0.001), mean pulmonary artery pressure (r = 0.41; P = 0.006), and pulmonary vascular resistance (r = 0.41; P = 0.007). TIFA protein expression could independently predict the presence of PAH (odds ratio [95% confidence interval per-0.1 standard deviation]: 1.72 [1.37–2.16]; P < 0.001) and outperformed echocardiographic estimation. Ex vivo silencing of TIFA protein expression in PBMCs led to the suppression of the cellular expression of IL-1β and TNF-α. IL-1β and TNF-α mediated 80.4% and 56.6% of the causal relationship between TIFA and PAH, respectively, supporting the idea that TIFA protein is involved in the pathogenesis of PAH. |
format | Online Article Text |
id | pubmed-8266829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82668292021-07-12 TIFA protein expression is associated with pulmonary arterial hypertension Chang, Hao-Chih Wei, Tong-You Wade Wu, Pei-Yu Tsai, Ming-Daw Yu, Wen-Chung Chen, Chen-Huan Sung, Shih-Hsien Sci Rep Article Tumor necrosis factor receptor-associated factor-interacting protein with a forkhead-associated domain (TIFA), a key regulator of inflammation, may be involved in the pathogenesis of pulmonary arterial hypertension (PAH). A total of 48 PAH patients (age 50.1 ± 13.1 years, 22.9% men), 25 hypertensive subjects, and 26 healthy controls were enrolled. TIFA protein expression in peripheral blood mononuclear cells (PBMCs) and plasma interleukin (IL)-1β and tumor necrosis factor (TNF)-α were measured. Pulmonary arterial hemodynamics were derived from right heart catheterization. PAH patients had the highest expression of TIFA, TNF-α, and IL-1β. TIFA protein expression was significantly associated with IL-1β (r = 0.94; P < 0.001), TNF-α (r = 0.93; P < 0.001), mean pulmonary artery pressure (r = 0.41; P = 0.006), and pulmonary vascular resistance (r = 0.41; P = 0.007). TIFA protein expression could independently predict the presence of PAH (odds ratio [95% confidence interval per-0.1 standard deviation]: 1.72 [1.37–2.16]; P < 0.001) and outperformed echocardiographic estimation. Ex vivo silencing of TIFA protein expression in PBMCs led to the suppression of the cellular expression of IL-1β and TNF-α. IL-1β and TNF-α mediated 80.4% and 56.6% of the causal relationship between TIFA and PAH, respectively, supporting the idea that TIFA protein is involved in the pathogenesis of PAH. Nature Publishing Group UK 2021-07-08 /pmc/articles/PMC8266829/ /pubmed/34238983 http://dx.doi.org/10.1038/s41598-021-93582-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Chang, Hao-Chih Wei, Tong-You Wade Wu, Pei-Yu Tsai, Ming-Daw Yu, Wen-Chung Chen, Chen-Huan Sung, Shih-Hsien TIFA protein expression is associated with pulmonary arterial hypertension |
title | TIFA protein expression is associated with pulmonary arterial hypertension |
title_full | TIFA protein expression is associated with pulmonary arterial hypertension |
title_fullStr | TIFA protein expression is associated with pulmonary arterial hypertension |
title_full_unstemmed | TIFA protein expression is associated with pulmonary arterial hypertension |
title_short | TIFA protein expression is associated with pulmonary arterial hypertension |
title_sort | tifa protein expression is associated with pulmonary arterial hypertension |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266829/ https://www.ncbi.nlm.nih.gov/pubmed/34238983 http://dx.doi.org/10.1038/s41598-021-93582-1 |
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