Cargando…
Chronic obstructive sleep apnea accelerates pulmonary remodeling via TGF-β/miR-185/CoLA1 signaling in a canine model
Chronic obstructive sleep apnea syndrome (OSAS) is considered to be associated with pulmonary diseases. However, the roles and mechanisms of OSA in pulmonary remodeling remain ambiguous. Thus, this study was aimed to elucidate the morphological and mechanical action of OSA in lung remodeling. In the...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295371/ https://www.ncbi.nlm.nih.gov/pubmed/27542203 http://dx.doi.org/10.18632/oncotarget.11296 |
_version_ | 1782505422893088768 |
---|---|
author | Ding, Xue Yu, Chengyuan Liu, Yang Yan, Sen Li, Wenpeng Wang, Dingyu Sun, Li Han, Yu Li, Minghui Zhang, Song Yun, Fengxiang Zhao, Hongwei Li, Yue |
author_facet | Ding, Xue Yu, Chengyuan Liu, Yang Yan, Sen Li, Wenpeng Wang, Dingyu Sun, Li Han, Yu Li, Minghui Zhang, Song Yun, Fengxiang Zhao, Hongwei Li, Yue |
author_sort | Ding, Xue |
collection | PubMed |
description | Chronic obstructive sleep apnea syndrome (OSAS) is considered to be associated with pulmonary diseases. However, the roles and mechanisms of OSA in pulmonary remodeling remain ambiguous. Thus, this study was aimed to elucidate the morphological and mechanical action of OSA in lung remodeling. In the present study, we employed a novel OSA model to mimic the OSA patient and investigate the role of OSA in pulmonary remodeling. We showed that pulmonary artery pressure of OSA group has no significant increased compared with the sham group. Nevertheless, we found that fibrotic tissue was predominantly located around the bronchi and vascular in the lung. Additionally, inflammatory cell infiltration was also detected in the peribonchial and perivascular space. The morphological change in OSA canines was ascertained by ultrastructure variation characterized by mitochondrial swelling, lamellar bodies degeneration and vascular smooth muscle incrassation. Moreover, sympathetic nerve sprouting was markedly increased in OSA group. Mechanistically, we showed that several pivotal proteins including collagen type I(CoLA1), GAP-43, TH and NGF were highly expressed in OSA groups. Furthermore, we found OSA could activated the expression of TGF-β, which subsequently suppressed miR-185 and promoted CoL A1 expression. This signaling cascade leads to pulmonary remodeling. In conclusion, Our data demonstrates that OSA can accelerate the progression of pulmonary remodeling through TGF-β/miR-185/CoLA1 signaling, which would potentially provide therapeutic strategies for chronic OSAS. |
format | Online Article Text |
id | pubmed-5295371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-52953712017-02-08 Chronic obstructive sleep apnea accelerates pulmonary remodeling via TGF-β/miR-185/CoLA1 signaling in a canine model Ding, Xue Yu, Chengyuan Liu, Yang Yan, Sen Li, Wenpeng Wang, Dingyu Sun, Li Han, Yu Li, Minghui Zhang, Song Yun, Fengxiang Zhao, Hongwei Li, Yue Oncotarget Research Paper: Pathology Chronic obstructive sleep apnea syndrome (OSAS) is considered to be associated with pulmonary diseases. However, the roles and mechanisms of OSA in pulmonary remodeling remain ambiguous. Thus, this study was aimed to elucidate the morphological and mechanical action of OSA in lung remodeling. In the present study, we employed a novel OSA model to mimic the OSA patient and investigate the role of OSA in pulmonary remodeling. We showed that pulmonary artery pressure of OSA group has no significant increased compared with the sham group. Nevertheless, we found that fibrotic tissue was predominantly located around the bronchi and vascular in the lung. Additionally, inflammatory cell infiltration was also detected in the peribonchial and perivascular space. The morphological change in OSA canines was ascertained by ultrastructure variation characterized by mitochondrial swelling, lamellar bodies degeneration and vascular smooth muscle incrassation. Moreover, sympathetic nerve sprouting was markedly increased in OSA group. Mechanistically, we showed that several pivotal proteins including collagen type I(CoLA1), GAP-43, TH and NGF were highly expressed in OSA groups. Furthermore, we found OSA could activated the expression of TGF-β, which subsequently suppressed miR-185 and promoted CoL A1 expression. This signaling cascade leads to pulmonary remodeling. In conclusion, Our data demonstrates that OSA can accelerate the progression of pulmonary remodeling through TGF-β/miR-185/CoLA1 signaling, which would potentially provide therapeutic strategies for chronic OSAS. Impact Journals LLC 2016-08-15 /pmc/articles/PMC5295371/ /pubmed/27542203 http://dx.doi.org/10.18632/oncotarget.11296 Text en Copyright: © 2016 Ding et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper: Pathology Ding, Xue Yu, Chengyuan Liu, Yang Yan, Sen Li, Wenpeng Wang, Dingyu Sun, Li Han, Yu Li, Minghui Zhang, Song Yun, Fengxiang Zhao, Hongwei Li, Yue Chronic obstructive sleep apnea accelerates pulmonary remodeling via TGF-β/miR-185/CoLA1 signaling in a canine model |
title | Chronic obstructive sleep apnea accelerates pulmonary remodeling via TGF-β/miR-185/CoLA1 signaling in a canine model |
title_full | Chronic obstructive sleep apnea accelerates pulmonary remodeling via TGF-β/miR-185/CoLA1 signaling in a canine model |
title_fullStr | Chronic obstructive sleep apnea accelerates pulmonary remodeling via TGF-β/miR-185/CoLA1 signaling in a canine model |
title_full_unstemmed | Chronic obstructive sleep apnea accelerates pulmonary remodeling via TGF-β/miR-185/CoLA1 signaling in a canine model |
title_short | Chronic obstructive sleep apnea accelerates pulmonary remodeling via TGF-β/miR-185/CoLA1 signaling in a canine model |
title_sort | chronic obstructive sleep apnea accelerates pulmonary remodeling via tgf-β/mir-185/cola1 signaling in a canine model |
topic | Research Paper: Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295371/ https://www.ncbi.nlm.nih.gov/pubmed/27542203 http://dx.doi.org/10.18632/oncotarget.11296 |
work_keys_str_mv | AT dingxue chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel AT yuchengyuan chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel AT liuyang chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel AT yansen chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel AT liwenpeng chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel AT wangdingyu chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel AT sunli chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel AT hanyu chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel AT liminghui chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel AT zhangsong chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel AT yunfengxiang chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel AT zhaohongwei chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel AT liyue chronicobstructivesleepapneaacceleratespulmonaryremodelingviatgfbmir185cola1signalinginacaninemodel |