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Adipocyte dysfunction promotes lung inflammation and aberrant repair: a potential target of COPD
BACKGROUND: Obesity and chronic obstructive pulmonary disease (COPD) are prevailing worldwide, bringing a heavy medical burden. Clinical and pathophysiological relationship between obesity and COPD is paradoxical and elusive. We aim to explore their inherent associations from clinical, genetic, and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10597776/ https://www.ncbi.nlm.nih.gov/pubmed/37886639 http://dx.doi.org/10.3389/fendo.2023.1204744 |
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author | Zhang, Si-jin Qin, Xian-zheng Zhou, Jie He, Bin-feng Shrestha, Surendra Zhang, Jing Hu, Wei-ping |
author_facet | Zhang, Si-jin Qin, Xian-zheng Zhou, Jie He, Bin-feng Shrestha, Surendra Zhang, Jing Hu, Wei-ping |
author_sort | Zhang, Si-jin |
collection | PubMed |
description | BACKGROUND: Obesity and chronic obstructive pulmonary disease (COPD) are prevailing worldwide, bringing a heavy medical burden. Clinical and pathophysiological relationship between obesity and COPD is paradoxical and elusive. We aim to explore their inherent associations from clinical, genetic, and animal levels. METHODS: We performed literature review and cohort analysis of patients with COPD to compare lung function, symptom, and prognosis among different weight groups. After retrieving datasets of obesity and COPD in Gene Expression Omnibus (GEO) database, we carried out differentially expressed gene analysis, functional enrichment, protein–protein interactions network, and weighted gene co-expression network analysis. Then, we acquired paraffin-embedded lung tissues of fatty acid–binding protein 4–Cre-BMPR2(fl/fl) conditional knockout (CKO) mice that were characterized by adipocyte-specific knockout of bone morphogenetic protein receptor 2 (BMPR2) for staining and analysis. RESULTS: Our cohort study reports the effect of obesity on COPD is inconsistent with previous clinical studies. Lung function of overweight group was statistically superior to that of other groups. We also found that the inflammatory factors were significantly increased hub genes, and cytokine-associated pathways were enriched in white adipose tissue of patients with obesity. Similarly, injury repair–associated genes and pathways were further enhanced in the small airways of patients with COPD. CKO mice spontaneously developed lung injury, emphysema, and pulmonary vascular remodeling, along with increased infiltration of macrophages. BMPR2-defiecient adipocytes had dysregulated expression of adipocytokines. CONCLUSION: Inflammation and abnormal repair might be potential mechanisms of the pathological association between obesity and COPD. BMPR2-associated adipocyte dysfunction promoted lung inflammation and aberrant repair, in which adipocytokines might play a role and thus could be a promising therapeutic target. |
format | Online Article Text |
id | pubmed-10597776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105977762023-10-26 Adipocyte dysfunction promotes lung inflammation and aberrant repair: a potential target of COPD Zhang, Si-jin Qin, Xian-zheng Zhou, Jie He, Bin-feng Shrestha, Surendra Zhang, Jing Hu, Wei-ping Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Obesity and chronic obstructive pulmonary disease (COPD) are prevailing worldwide, bringing a heavy medical burden. Clinical and pathophysiological relationship between obesity and COPD is paradoxical and elusive. We aim to explore their inherent associations from clinical, genetic, and animal levels. METHODS: We performed literature review and cohort analysis of patients with COPD to compare lung function, symptom, and prognosis among different weight groups. After retrieving datasets of obesity and COPD in Gene Expression Omnibus (GEO) database, we carried out differentially expressed gene analysis, functional enrichment, protein–protein interactions network, and weighted gene co-expression network analysis. Then, we acquired paraffin-embedded lung tissues of fatty acid–binding protein 4–Cre-BMPR2(fl/fl) conditional knockout (CKO) mice that were characterized by adipocyte-specific knockout of bone morphogenetic protein receptor 2 (BMPR2) for staining and analysis. RESULTS: Our cohort study reports the effect of obesity on COPD is inconsistent with previous clinical studies. Lung function of overweight group was statistically superior to that of other groups. We also found that the inflammatory factors were significantly increased hub genes, and cytokine-associated pathways were enriched in white adipose tissue of patients with obesity. Similarly, injury repair–associated genes and pathways were further enhanced in the small airways of patients with COPD. CKO mice spontaneously developed lung injury, emphysema, and pulmonary vascular remodeling, along with increased infiltration of macrophages. BMPR2-defiecient adipocytes had dysregulated expression of adipocytokines. CONCLUSION: Inflammation and abnormal repair might be potential mechanisms of the pathological association between obesity and COPD. BMPR2-associated adipocyte dysfunction promoted lung inflammation and aberrant repair, in which adipocytokines might play a role and thus could be a promising therapeutic target. Frontiers Media S.A. 2023-10-10 /pmc/articles/PMC10597776/ /pubmed/37886639 http://dx.doi.org/10.3389/fendo.2023.1204744 Text en Copyright © 2023 Zhang, Qin, Zhou, He, Shrestha, Zhang and Hu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Zhang, Si-jin Qin, Xian-zheng Zhou, Jie He, Bin-feng Shrestha, Surendra Zhang, Jing Hu, Wei-ping Adipocyte dysfunction promotes lung inflammation and aberrant repair: a potential target of COPD |
title | Adipocyte dysfunction promotes lung inflammation and aberrant repair: a potential target of COPD |
title_full | Adipocyte dysfunction promotes lung inflammation and aberrant repair: a potential target of COPD |
title_fullStr | Adipocyte dysfunction promotes lung inflammation and aberrant repair: a potential target of COPD |
title_full_unstemmed | Adipocyte dysfunction promotes lung inflammation and aberrant repair: a potential target of COPD |
title_short | Adipocyte dysfunction promotes lung inflammation and aberrant repair: a potential target of COPD |
title_sort | adipocyte dysfunction promotes lung inflammation and aberrant repair: a potential target of copd |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10597776/ https://www.ncbi.nlm.nih.gov/pubmed/37886639 http://dx.doi.org/10.3389/fendo.2023.1204744 |
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