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The development of nasal polyps involves early middle meatus mucous remodeling via TGF-β1 mediated PAI-1 reduction()

OBJECTIVE: Our study aimed to elucidate the effect of PAI-1 (Plasminogen Activator Inhibitor-1) and t-PA (Tissue-type Plasminogen Activator) in tissue remodeling in nasal polyps patients. METHODS: Samples were streamed as early Nasal Polyps (eNP, n = 10) and inferior tissue from the same patient, ma...

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Autores principales: Liu, Yijun, Shu, Longlan, Jiang, Xiaocong, Zhang, Yue, Chen, Qian, Shen, Yang, Yang, Yucheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164765/
https://www.ncbi.nlm.nih.gov/pubmed/36841712
http://dx.doi.org/10.1016/j.bjorl.2023.01.007
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author Liu, Yijun
Shu, Longlan
Jiang, Xiaocong
Zhang, Yue
Chen, Qian
Shen, Yang
Yang, Yucheng
author_facet Liu, Yijun
Shu, Longlan
Jiang, Xiaocong
Zhang, Yue
Chen, Qian
Shen, Yang
Yang, Yucheng
author_sort Liu, Yijun
collection PubMed
description OBJECTIVE: Our study aimed to elucidate the effect of PAI-1 (Plasminogen Activator Inhibitor-1) and t-PA (Tissue-type Plasminogen Activator) in tissue remodeling in nasal polyps patients. METHODS: Samples were streamed as early Nasal Polyps (eNP, n = 10) and inferior tissue from the same patient, mature Nasal Polyps (mNP, n = 14), and Control group (n = 15), respectively. Immunohistochemistry and immunofluorescence were applied to detect localization. Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR) and Western blot were used to measure different levels among three groups. The mNP tissue was cultured in vitro and treated with TGF-β1 (Transforming Growth Factor-beta 1) activator, TGF-β1 inhibitor (SB431542), and PAI-1 inhibitor (TM5275); then Western blot, qRT-PCR, and ELISA were used to assess changes. RESULTS: The immunohistochemistry and immunofluorescence showed that PAI-1 expression decreased in eNP and mNP, mainly in epithelium and glands. The transcriptional expression and protein level of TGF-β1/t-PA/PAI-1/Collagen1 were lower in eNP than IT while mNP group demonstrated lower mRNA expression and protein level of TGF-β1/t-PA/PAI-1/Collagen1 than Control group. In mNP tissue culture in vitro, TGF-β1 activator elevated t-PA, PAI-1, and Collagen1 with higher release of PAI-1 and Collagen1 in supernatant, whereas SB431542 suppressed above reactions; TM5275 lowered transcriptional and protein level of Collagen1 in supernatant. CONCLUSION: Early Nasal polyps’ formation in middle meatus mucous is related with fibrillation system PAI-1/t-PA and tissue remodeling; moreover, nasal polyps’ development is regulated by TGF-β1-mediated PAI-1 reduction. LEVEL OF EVIDENCE: 3b.
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spelling pubmed-101647652023-05-09 The development of nasal polyps involves early middle meatus mucous remodeling via TGF-β1 mediated PAI-1 reduction() Liu, Yijun Shu, Longlan Jiang, Xiaocong Zhang, Yue Chen, Qian Shen, Yang Yang, Yucheng Braz J Otorhinolaryngol Original Article OBJECTIVE: Our study aimed to elucidate the effect of PAI-1 (Plasminogen Activator Inhibitor-1) and t-PA (Tissue-type Plasminogen Activator) in tissue remodeling in nasal polyps patients. METHODS: Samples were streamed as early Nasal Polyps (eNP, n = 10) and inferior tissue from the same patient, mature Nasal Polyps (mNP, n = 14), and Control group (n = 15), respectively. Immunohistochemistry and immunofluorescence were applied to detect localization. Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR) and Western blot were used to measure different levels among three groups. The mNP tissue was cultured in vitro and treated with TGF-β1 (Transforming Growth Factor-beta 1) activator, TGF-β1 inhibitor (SB431542), and PAI-1 inhibitor (TM5275); then Western blot, qRT-PCR, and ELISA were used to assess changes. RESULTS: The immunohistochemistry and immunofluorescence showed that PAI-1 expression decreased in eNP and mNP, mainly in epithelium and glands. The transcriptional expression and protein level of TGF-β1/t-PA/PAI-1/Collagen1 were lower in eNP than IT while mNP group demonstrated lower mRNA expression and protein level of TGF-β1/t-PA/PAI-1/Collagen1 than Control group. In mNP tissue culture in vitro, TGF-β1 activator elevated t-PA, PAI-1, and Collagen1 with higher release of PAI-1 and Collagen1 in supernatant, whereas SB431542 suppressed above reactions; TM5275 lowered transcriptional and protein level of Collagen1 in supernatant. CONCLUSION: Early Nasal polyps’ formation in middle meatus mucous is related with fibrillation system PAI-1/t-PA and tissue remodeling; moreover, nasal polyps’ development is regulated by TGF-β1-mediated PAI-1 reduction. LEVEL OF EVIDENCE: 3b. Elsevier 2023-02-14 /pmc/articles/PMC10164765/ /pubmed/36841712 http://dx.doi.org/10.1016/j.bjorl.2023.01.007 Text en © 2023 Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial. Published by Elsevier España, S.L.U. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Liu, Yijun
Shu, Longlan
Jiang, Xiaocong
Zhang, Yue
Chen, Qian
Shen, Yang
Yang, Yucheng
The development of nasal polyps involves early middle meatus mucous remodeling via TGF-β1 mediated PAI-1 reduction()
title The development of nasal polyps involves early middle meatus mucous remodeling via TGF-β1 mediated PAI-1 reduction()
title_full The development of nasal polyps involves early middle meatus mucous remodeling via TGF-β1 mediated PAI-1 reduction()
title_fullStr The development of nasal polyps involves early middle meatus mucous remodeling via TGF-β1 mediated PAI-1 reduction()
title_full_unstemmed The development of nasal polyps involves early middle meatus mucous remodeling via TGF-β1 mediated PAI-1 reduction()
title_short The development of nasal polyps involves early middle meatus mucous remodeling via TGF-β1 mediated PAI-1 reduction()
title_sort development of nasal polyps involves early middle meatus mucous remodeling via tgf-β1 mediated pai-1 reduction()
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10164765/
https://www.ncbi.nlm.nih.gov/pubmed/36841712
http://dx.doi.org/10.1016/j.bjorl.2023.01.007
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