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The role and mechanism of 1,25-dihydroxyvitamin D(3) in regulating the Rho-kinase signaling pathway in asthmatic rats

BACKGROUND: Bronchial asthma (referred to as asthma in the present study) is the most common chronic airway inflammatory disease in childhood. The present study aimed to investigate the effect of 1,25-dihydroxyvitamin D(3) [1,25-(OH)(2)D(3)] on VDR expression, which is closely associated with asthma...

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Detalles Bibliográficos
Autores principales: Tian, Wei-Min, Chen, Wei-Wei, Chen, Yu, Lin, Chen-Xi, Huang, Jin-Xian, Song, Ya-Ping, Yang, Yun-Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107869/
https://www.ncbi.nlm.nih.gov/pubmed/34012827
http://dx.doi.org/10.21037/tp-20-365
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author Tian, Wei-Min
Chen, Wei-Wei
Chen, Yu
Lin, Chen-Xi
Huang, Jin-Xian
Song, Ya-Ping
Yang, Yun-Gang
author_facet Tian, Wei-Min
Chen, Wei-Wei
Chen, Yu
Lin, Chen-Xi
Huang, Jin-Xian
Song, Ya-Ping
Yang, Yun-Gang
author_sort Tian, Wei-Min
collection PubMed
description BACKGROUND: Bronchial asthma (referred to as asthma in the present study) is the most common chronic airway inflammatory disease in childhood. The present study aimed to investigate the effect of 1,25-dihydroxyvitamin D(3) [1,25-(OH)(2)D(3)] on VDR expression, which is closely associated with asthmatic airway smooth muscle cells (ASMCs), and explored its role and mechanism in the Rho-kinase signaling pathway. METHODS: The acute asthma model was induced by ovalbumin (OVA) and pertussis bacillus, and ASMCs obtained from asthmatic rats were cultured in vitro. These cells were randomly divided into five groups: control (N) group, TNF-α (TNF) group, 1,25-(OH)(2)D(3) (VD) group, dexamethasone (DXM) group, and 1,25-(OH)(2)D(3) + DXM (L) group. The protein expression levels of VDR, ROCK, MLC20 and P-MLC20 were detected by western blot, and the mRNA expression levels of VDR, ROCK, MLC20 and P-MLC20 were detected by real-time quantitative PCR. RESULTS: The expression of ROCK, MLC20 and P-MLC20 in each treatment group were significantly lower, when compared to the TNF group (P<0.05), but this remained stronger than (P<0.05) or similar to (P>0.05) that in the N group. CONCLUSIONS: The regulation mechanism of 1,25-(OH)(2)D(3) in alleviating asthma should be correlated to its regulation of the expression of related signaling molecules in the Rho-kinase signaling pathway, and this effect may be achieved by regulating the mRNA and protein expression of the VDR gene.
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spelling pubmed-81078692021-05-18 The role and mechanism of 1,25-dihydroxyvitamin D(3) in regulating the Rho-kinase signaling pathway in asthmatic rats Tian, Wei-Min Chen, Wei-Wei Chen, Yu Lin, Chen-Xi Huang, Jin-Xian Song, Ya-Ping Yang, Yun-Gang Transl Pediatr Original Article BACKGROUND: Bronchial asthma (referred to as asthma in the present study) is the most common chronic airway inflammatory disease in childhood. The present study aimed to investigate the effect of 1,25-dihydroxyvitamin D(3) [1,25-(OH)(2)D(3)] on VDR expression, which is closely associated with asthmatic airway smooth muscle cells (ASMCs), and explored its role and mechanism in the Rho-kinase signaling pathway. METHODS: The acute asthma model was induced by ovalbumin (OVA) and pertussis bacillus, and ASMCs obtained from asthmatic rats were cultured in vitro. These cells were randomly divided into five groups: control (N) group, TNF-α (TNF) group, 1,25-(OH)(2)D(3) (VD) group, dexamethasone (DXM) group, and 1,25-(OH)(2)D(3) + DXM (L) group. The protein expression levels of VDR, ROCK, MLC20 and P-MLC20 were detected by western blot, and the mRNA expression levels of VDR, ROCK, MLC20 and P-MLC20 were detected by real-time quantitative PCR. RESULTS: The expression of ROCK, MLC20 and P-MLC20 in each treatment group were significantly lower, when compared to the TNF group (P<0.05), but this remained stronger than (P<0.05) or similar to (P>0.05) that in the N group. CONCLUSIONS: The regulation mechanism of 1,25-(OH)(2)D(3) in alleviating asthma should be correlated to its regulation of the expression of related signaling molecules in the Rho-kinase signaling pathway, and this effect may be achieved by regulating the mRNA and protein expression of the VDR gene. AME Publishing Company 2021-04 /pmc/articles/PMC8107869/ /pubmed/34012827 http://dx.doi.org/10.21037/tp-20-365 Text en 2021 Translational Pediatrics. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Tian, Wei-Min
Chen, Wei-Wei
Chen, Yu
Lin, Chen-Xi
Huang, Jin-Xian
Song, Ya-Ping
Yang, Yun-Gang
The role and mechanism of 1,25-dihydroxyvitamin D(3) in regulating the Rho-kinase signaling pathway in asthmatic rats
title The role and mechanism of 1,25-dihydroxyvitamin D(3) in regulating the Rho-kinase signaling pathway in asthmatic rats
title_full The role and mechanism of 1,25-dihydroxyvitamin D(3) in regulating the Rho-kinase signaling pathway in asthmatic rats
title_fullStr The role and mechanism of 1,25-dihydroxyvitamin D(3) in regulating the Rho-kinase signaling pathway in asthmatic rats
title_full_unstemmed The role and mechanism of 1,25-dihydroxyvitamin D(3) in regulating the Rho-kinase signaling pathway in asthmatic rats
title_short The role and mechanism of 1,25-dihydroxyvitamin D(3) in regulating the Rho-kinase signaling pathway in asthmatic rats
title_sort role and mechanism of 1,25-dihydroxyvitamin d(3) in regulating the rho-kinase signaling pathway in asthmatic rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107869/
https://www.ncbi.nlm.nih.gov/pubmed/34012827
http://dx.doi.org/10.21037/tp-20-365
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